Dietary Fiber and Gut Microbiota: Surprising Key Effects
Discover how ‘dietary fiber and gut microbiota’ interact to boost your health. Learn the critical role fiber plays in gut ecosystem balance.

Dietary fiber and gut microbiota have a crucial impact on our health.
The relationship between dietary fiber and gut microbiota is complex.
Dietary fiber plays a significant role in maintaining overall health.
Gut microbiota is influenced by dietary fiber intake.
Understanding the connection between dietary fiber and gut microbiota is important for our well-being.

Main Findings
- Increased dietary fiber consumption positively influences metabolic health by altering gut microbiota.
- Dietary fiber affects gut microbiota composition and function, enriching certain species adapted to environmental changes in the ecosystem.
- These changes can lead to increased production of short-chain fatty acids (SCFAs), which can reduce metabolic syndrome symptoms like hyperlipidemia, hyperglycemia, hyperinsulinemia, and hypercholesterolemia.
- Further research is needed to fully understand dietary fiber–microbiome interactions, but increasing habitual fiber intake is seen as a promising and cost-effective method to reduce the burden of metabolic disease.
Introduction to Dietary Fiber
The human gastrointestinal tract (GIT) houses a complex microbial ecosystem with around 3.3 million microbial genes in the gut microbiota ✅ Trusted Source
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Qin, J.; Li, R.; Raes, J.; Arumugam, M.; Burgdorf, K.S.; Manichanh, C.; Nielsen, T.; Pons, N.; Levenez, F.; Yamada, T.; et al. A human gut microbial gene catalogue established by metagenomic sequencing. Nature 2010, 464, 59–65.
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Diet, antibiotics, exercise, age, and metabolic diseases like obesity, T2DM, and CVD influence microbial signatures ✅ Trusted Source
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Bäckhed, F.; Ley, R.E.; Sonnenburg, J.L.; Peterson, D.A.; Gordon, J.I. Host-bacterial mutualism in the human intestine. Science 2005, 307, 1915–1920.
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Singh, R.K.; Chang, H.-W.; Yan, D.; Lee, K.M.; Ucmak, D.; Wong, K.; Abrouk, M.; Farahnik, B.; Nakamura, M.; Zhu, T.H.; et al. Influence of diet on the gut microbiome and implications for human health. J. Transl. Med. 2017, 15, 1–17.
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Ferrer, M.; Méndez-García, C.; Rojo, D.; Barbas, C.; Moya, A. Antibiotic use and microbiome function. Biochem. Pharmacol. 2017, 134, 114–126.
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Tang, W.W.; Hazen, S.L. The contributory role of gut microbiota in cardiovascular disease. J. Clin. Investig. 2014, 124, 4204–4211.
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A low-fiber Western diet links to increased metabolic diseases ✅ Trusted Source
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Van Dam, R.M.; Rimm, E.B.; Willett, W.C.; Stampfer, M.J.; Hu, F.B. Dietary Patterns and Risk for Type 2 Diabetes Mellitus in U.S. Men. Ann. Intern. Med. 2002, 136, 201–209.
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Lutsey, P.L.; Steffen, L.M.; Stevens, J. Dietary Intake and the Development of the Metabolic Syndrome. Circulation 2008, 117, 754–761.
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To improve health and prevent diseases, methods like fecal microbial transplants (FMT) modify gut microbes.
Dietary fiber intervention also reshapes the microbiota for better health ✅ Trusted Source
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Fuentes, S.; van Nood, E.; Tims, S.; Jong, I.H.-D.; Ter-Braak, C.J.; Keller, J.J.; Zoetendal, E.G.; de Vos, W.M. Reset of a critically disturbed microbial ecosystem: Faecal transplant in recurrent Clostridium difficile infection. ISME J. 2014, 8, 1621–1633.
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O’Grady, J.; O’Connor, E.M.; Shanahan, F. Review article: Dietary fibre in the era of microbiome science. Aliment. Pharmacol. Ther. 2019, 49, 506–515.
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Evidence from studies shows that different dietary fibers and their fermentation products, like short-chain fatty acids (SCFAs), benefit metabolism ✅ Trusted Source
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den Besten, G.; Van Eunen, K.; Groen, A.K.; Venema, K.; Reijngoud, D.J.; Bakker, B.M. The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism. J. Lipid Res. 2013, 54, 2325–2340.
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SCFAs from fiber fermentation in the colon help regulate glucose and lipid metabolism ✅ Trusted Source
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den Besten, G.; Van Eunen, K.; Groen, A.K.; Venema, K.; Reijngoud, D.J.; Bakker, B.M. The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism. J. Lipid Res. 2013, 54, 2325–2340.
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Understanding how specific fibers impact microbiota and their metabolic effects offers therapeutic potential for metabolic diseases.
Understanding Dietary Fiber
Dietary fiber, plant-based carbs indigestible by our enzymes, undergo anaerobic fermentation by specific gut microbes, producing short-chain fatty acids (SCFAs) ✅ Trusted Source
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de Menezes, E.W.; Giuntini, E.B.; Dan, M.C.T.; Sardá, F.A.H.; Lajolo, F.M. Codex dietary fibre definition—Justification for inclusion of carbohydrates from 3 to 9 degrees of polymerisation. Food Chem. 2013, 140, 581–585.
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Definitions of dietary fiber vary globally; European standards accept fibers with 3 monomeric units, while others require at least 10 ✅ Trusted Source
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Stephen, A.M.; Champ, M.M.-J.; Cloran, S.J.; Fleith, M.; Van Lieshout, L.; Mejborn, H.; Burley, V.J. Dietary fibre in Europe: Current state of knowledge on definitions, sources, recommendations, intakes and relationships to health. Nutr. Res. Rev. 2017, 30, 149–190.
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Makki, K.; Deehan, E.C.; Walter, J.; Bäckhed, F. The Impact of Dietary Fiber on Gut Microbiota in Host Health and Disease. Cell Host Microbe 2018, 23, 705–715.
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Fibers with ≥10 units include cellulose, hemicellulose, gums, pectin, mucilage, inulin, psyllium, β-glucan, and resistant starch (RS) ✅ Trusted Source
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O’Grady, J.; O’Connor, E.M.; Shanahan, F. Review article: Dietary fibre in the era of microbiome science. Aliment. Pharmacol. Ther. 2019, 49, 506–515.
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Those with 3-9 units are called resistant oligosaccharides, like GOS and FOS ✅ Trusted Source
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Eswaran, S.; Muir, J.; Chey, W.D. Fiber and Functional Gastrointestinal Disorders. Am. J. Gastroenterol. 2013, 108, 718–727.
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Despite differing definitions, all fiber types influence gut microbiota, affecting host metabolism.
Fiber's impact on the host relies on properties like solubility, viscosity, and fermentability, which vary across types ✅ Trusted Source
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Bijkerk, C.J.; Muris, J.W.M.; Knottnerus, J.A.; Hoes, A.W.; De Wit, N.J. Systematic review: The role of different types of fibre in the treatment of irritable bowel syndrome. Aliment. Pharmacol. Ther. 2004, 19, 245–251.
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Solubility refers to water dissolution, fermentability indicates microbial metabolism, and viscosity describes gel-like formation in water.
"Microbiota-accessible carbohydrate" (MAC) excludes insoluble fibers.
Highly soluble, fermentable, and viscous fibers, such as β-glucan, gums, and pectin, are examples ✅ Trusted Source
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Dhingra, D.; Michael, M.; Rajput, H.; Patil, R.T. Dietary fibre in foods: A review. J. Food Sci. Technol. 2011, 49, 255–266.
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How Fiber Shapes Our Gut Bacteria
Dietary fiber wields significant influence over the composition, diversity, and richness of the gut microbiome by providing a range of substrates for fermentation reactions carried out by specific microbe species with the necessary enzymatic machinery ✅ Trusted Source
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Walter, J. Murine Gut Microbiota—Diet Trumps Genes. Cell Host Microbe 2015, 17, 3–5.
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The large intestine hosts numerous microbiota species specializing in fiber fermentation, and various types of dietary fiber undergo breakdown.
When dietary fiber intake increases, it alters the nutritional environment in the intestines, allowing these fiber-loving bacteria to thrive ✅ Trusted Source
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Walter, J. Murine Gut Microbiota—Diet Trumps Genes. Cell Host Microbe 2015, 17, 3–5.
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Conversely, those with low fiber diets tend to exhibit reduced microbial diversity, as their diets often feature animal proteins and fats instead ✅ Trusted Source
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Makki, K.; Deehan, E.C.; Walter, J.; Bäckhed, F. The Impact of Dietary Fiber on Gut Microbiota in Host Health and Disease. Cell Host Microbe 2018, 23, 705–715.
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Studies from different regions and socioeconomic backgrounds consistently highlight the impact of diet on human gastrointestinal tract microbial populations ✅ Trusted Source
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De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696.
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Yatsunenko, T.; Rey, F.E.; Manary, M.J.; Trehan, I.; Dominguez-Bello, M.G.; Contreras, M.; Magris, M.; Hidalgo, G.; Baldassano, R.N.; Anokhin, A.P.; et al. Human gut microbiome viewed across age and geography. Nature 2012, 486, 222–227.
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Ou, J.; Carbonero, F.; Zoetendal, E.G.; Delany, J.P.; Wang, M.; Newton, K.; Gaskins, H.R.; O’Keefe, S.J.D. Diet, microbiota, and microbial metabolites in colon cancer risk in rural Africans and African Americans. Am. J. Clin. Nutr. 2013, 98, 111–120.
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David, L.A.; Maurice, C.F.; Carmody, R.N.; Gootenberg, D.B.; Button, J.E.; Wolfe, B.E.; Ling, A.V.; Devlin, A.S.; Varma, Y.; Fischbach, M.A.; et al. Diet rapidly and reproducibly alters the human gut microbiome. Nat. Cell Biol. 2014, 505, 559–563.
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Schnorr, S.L.; Candela, M.; Rampelli, S.; Centanni, M.; Consolandi, C.; Basaglia, G.; Turroni, S.; Biagi, E.; Peano, C.; Severgnini, M.; et al. Gut microbiome of the Hadza hunter-gatherers. Nat. Commun. 2014, 5, 3654.
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Sonnenburg, E.D.; Sonnenburg, J.L. Starving our Microbial Self: The Deleterious Consequences of a Diet Deficient in Mi-crobiota-Accessible Carbohydrates. Cell Metab. 2014, 20, 779–786.
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Clemente, J.C.; Pehrsson, E.C.; Blaser, M.J.; Sandhu, K.; Gao, Z.; Wang, B.; Magris, M.; Hidalgo, G.; Contreras, M.; Noya-Alarcón, Ó.; et al. The microbiome of uncontacted Amerindians. Sci. Adv. 2015, 1, e1500183.
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Martínez, I.; Stegen, J.C.; Maldonado-Gómez, M.X.; Eren, A.M.; Siba, P.M.; Greenhill, A.R.; Walter, J. The Gut Microbiota of Rural Papua New Guineans: Composition, Diversity Patterns, and Ecological Processes. Cell Rep. 2015, 11, 527–538.
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De Filippo, C.; Di Paola, M.; Ramazzotti, M.; Albanese, D.; Pieraccini, G.; Banci, E.; Miglietta, F.; Cavalieri, D.; Lionetti, P. Diet, Environments, and Gut Microbiota. A Preliminary Investigation in Children Living in Rural and Urban Burkina Faso and Italy. Front. Microbiol. 2017, 8, 1979.
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One common thread is the significantly higher fiber consumption among individuals in less developed and rural societies compared to those in industrialized nations ✅ Trusted Source
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De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696.
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✅ Trusted Source
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Sonnenburg, E.D.; Sonnenburg, J.L. Starving our Microbial Self: The Deleterious Consequences of a Diet Deficient in Mi-crobiota-Accessible Carbohydrates. Cell Metab. 2014, 20, 779–786.
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Intriguingly, industrialized nations, characterized by low fiber intake, often experience a higher prevalence of metabolic and inflammatory diseases like obesity and IBD.

For instance, De Filippo et al. (2010) ✅ Trusted Source
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De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696.
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found differences in gut microbiomes between Burkina Fasian and Italian children.
Burkina Fasian children displayed higher levels of Actinobacteria, Bacteroidetes, and Prevotella, whereas Italian children exhibited a higher abundance of Firmicutes and Proteobacteria ✅ Trusted Source
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De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696.
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A similar study by the same author comparing four cohorts with varying degrees of urbanization noted reduced fiber consumption among urban Italian and urban Burkina Faso children, reflected in lower Prevotella species in their microbiota ✅ Trusted Source
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De Filippo, C.; Di Paola, M.; Ramazzotti, M.; Albanese, D.; Pieraccini, G.; Banci, E.; Miglietta, F.; Cavalieri, D.; Lionetti, P. Diet, Environments, and Gut Microbiota. A Preliminary Investigation in Children Living in Rural and Urban Burkina Faso and Italy. Front. Microbiol. 2017, 8, 1979.
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These microbiota differences mirrored those reported by Ou et al. (2013) ✅ Trusted Source
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Ou, J.; Carbonero, F.; Zoetendal, E.G.; Delany, J.P.; Wang, M.; Newton, K.; Gaskins, H.R.; O’Keefe, S.J.D. Diet, microbiota, and microbial metabolites in colon cancer risk in rural Africans and African Americans. Am. J. Clin. Nutr. 2013, 98, 111–120.
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when comparing rural South Africans with African Americans.
In 2015, a study comparing the microbiota of Papua New Guineans with Americans revealed an altered Prevotella:Bacteroides ratio in the fecal microbiota of Papua New Guineans, who consumed a fiber-rich diet.
They exhibited a high abundance of Prevotella but a low abundance of Faecalibacterium, Ruminococcus, Bifidobacterium, Bacteroides, Blautia, Bilophila, and Alistipes ✅ Trusted Source
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Martínez, I.; Stegen, J.C.; Maldonado-Gómez, M.X.; Eren, A.M.; Siba, P.M.; Greenhill, A.R.; Walter, J. The Gut Microbiota of Rural Papua New Guineans: Composition, Diversity Patterns, and Ecological Processes. Cell Rep. 2015, 11, 527–538.
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Yatsunenko et al. (2012) ✅ Trusted Source
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Yatsunenko, T.; Rey, F.E.; Manary, M.J.; Trehan, I.; Dominguez-Bello, M.G.; Contreras, M.; Magris, M.; Hidalgo, G.; Baldassano, R.N.; Anokhin, A.P.; et al. Human gut microbiome viewed across age and geography. Nature 2012, 486, 222–227.
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found similar results when comparing individuals from Venezuela, Malawi, and the USA.
Another study investigated the microbiota of the Yanomami tribe in rural Venezuela, revealing a higher abundance of Prevotella and a lower abundance of Bacteroides compared to individuals from the USA ✅ Trusted Source
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Clemente, J.C.; Pehrsson, E.C.; Blaser, M.J.; Sandhu, K.; Gao, Z.; Wang, B.; Magris, M.; Hidalgo, G.; Contreras, M.; Noya-Alarcón, Ó.; et al. The microbiome of uncontacted Amerindians. Sci. Adv. 2015, 1, e1500183.
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Additionally, the Yanomami population had lower levels of other Bacteroidetes family members, including Bacteroidales, Mollicutes, and Verrucomicrobia, and an increased abundance of the genus Phascolarctobacterium, known for SCFA production ✅ Trusted Source
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Wu, F.; Guo, X.; Zhang, J.; Zhang, M.; Ou, Z.; Peng, Y. Phascolarctobacterium faecium abundant colonization in human gastrointestinal tract. Exp. Ther. Med. 2017, 14, 3122–3126.
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A study comparing the Tanzanian Hadza tribe to Italians found an abundance of well-known fiber-degrading bacteria in both populations, including Firmicutes families like Lachnospiraceae, Ruminococcaceae, Veillonellaceae, Clostridiales Incertae Sedis XIV, and Clostridiaceae.
Similar to other studies, Prevotella was enriched in the Hadza microbiome, while their Italian counterparts had a lower abundance of Bacteroides ✅ Trusted Source
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Schnorr, S.L.; Candela, M.; Rampelli, S.; Centanni, M.; Consolandi, C.; Basaglia, G.; Turroni, S.; Biagi, E.; Peano, C.; Severgnini, M.; et al. Gut microbiome of the Hadza hunter-gatherers. Nat. Commun. 2014, 5, 3654.
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Another study in the USA linked higher Prevotella levels to fiber degradation and reported correlations with Roseburia, Eubacterium rectale, Faecalibacterium prausnitzii, and increased total SCFAs concentrations in response to a plant-based diet ✅ Trusted Source
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David, L.A.; Maurice, C.F.; Carmody, R.N.; Gootenberg, D.B.; Button, J.E.; Wolfe, B.E.; Ling, A.V.; Devlin, A.S.; Varma, Y.; Fischbach, M.A.; et al. Diet rapidly and reproducibly alters the human gut microbiome. Nat. Cell Biol. 2014, 505, 559–563.
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These findings underscore the profound impact of dietary fiber on the microbiota.
Industrialized nations typically exhibit higher abundances of Bacteroides, Bifidobacterium, Ruminococcus, Faecalibacterium, Alistipes, Bilophila, and Blautia ✅ Trusted Source
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De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696.
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Yatsunenko, T.; Rey, F.E.; Manary, M.J.; Trehan, I.; Dominguez-Bello, M.G.; Contreras, M.; Magris, M.; Hidalgo, G.; Baldassano, R.N.; Anokhin, A.P.; et al. Human gut microbiome viewed across age and geography. Nature 2012, 486, 222–227.
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✅ Trusted Source
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Schnorr, S.L.; Candela, M.; Rampelli, S.; Centanni, M.; Consolandi, C.; Basaglia, G.; Turroni, S.; Biagi, E.; Peano, C.; Severgnini, M.; et al. Gut microbiome of the Hadza hunter-gatherers. Nat. Commun. 2014, 5, 3654.
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✅ Trusted Source
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Martínez, I.; Stegen, J.C.; Maldonado-Gómez, M.X.; Eren, A.M.; Siba, P.M.; Greenhill, A.R.; Walter, J. The Gut Microbiota of Rural Papua New Guineans: Composition, Diversity Patterns, and Ecological Processes. Cell Rep. 2015, 11, 527–538.
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✅ Trusted Source
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De Filippo, C.; Di Paola, M.; Ramazzotti, M.; Albanese, D.; Pieraccini, G.; Banci, E.; Miglietta, F.; Cavalieri, D.; Lionetti, P. Diet, Environments, and Gut Microbiota. A Preliminary Investigation in Children Living in Rural and Urban Burkina Faso and Italy. Front. Microbiol. 2017, 8, 1979.
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Surprisingly, cultural and ethnic differences have minimal effects on the host microbiota, as evidenced by minimal variations in microbiota among industrialized nations that share a common Western diet ✅ Trusted Source
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David, L.A.; Maurice, C.F.; Carmody, R.N.; Gootenberg, D.B.; Button, J.E.; Wolfe, B.E.; Ling, A.V.; Devlin, A.S.; Varma, Y.; Fischbach, M.A.; et al. Diet rapidly and reproducibly alters the human gut microbiome. Nat. Cell Biol. 2014, 505, 559–563.
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Wu, G.D.; Chen, J.; Hoffmann, C.; Bittinger, K.; Chen, Y.Y.; Keilbaugh, S.A.; Bewtra, M.; Knights, D.; Walters, W.A.; Knight, R.; et al. Linking Long-Term Dietary Patterns with Gut Microbial Enterotypes. Science 2011, 334, 105–108.
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, high in saturated fat and low in fiber.
Prevotella species are more abundant in non-industrialized individuals with high fiber diets.
Interestingly, the microbiota of these non-industrialized populations mirrors those of Western vegans and vegetarians, all of whom consume ample dietary fiber ✅ Trusted Source
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David, L.A.; Maurice, C.F.; Carmody, R.N.; Gootenberg, D.B.; Button, J.E.; Wolfe, B.E.; Ling, A.V.; Devlin, A.S.; Varma, Y.; Fischbach, M.A.; et al. Diet rapidly and reproducibly alters the human gut microbiome. Nat. Cell Biol. 2014, 505, 559–563.
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High fiber intake, combined with specific fiber-fermenting microbes, offers various health benefits, including substantial SCFA production.
The Connection Between Dietary Fiber and Gut Microbiota
Dietary fiber is a powerful influencer of gut microbiota composition.
It offers a rich array of substrates for fermentation reactions carried out by various microbial enzymes in the large intestine.
Different types of fiber may require multiple enzymatic steps to yield short-chain fatty acid (SCFA) products, involving numerous microbial players.
Some microbes specialize in fiber degradation and are known as primary degraders or keystone species ✅ Trusted Source
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Flint, H.J.; Scott, K.P.; Louis, P.; Duncan, S.H. The role of the gut microbiota in nutrition and health. Nat. Rev. Gastroenterol. Hepatol. 2012, 9, 577–589.
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Ze, X.; Duncan, S.H.; Louis, P.; Flint, H.J. Ruminococcus bromii is a keystone species for the degradation of resistant starch in the human colon. ISME J. 2012, 6, 1535–1543.
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Meanwhile, others play minor roles, referred to as secondary fermenters or cross-feeders, benefiting from the work of primary degraders.
Remarkably, certain members of the colonic microbial community, such as Bacteroides thetaiotaomicron, exhibit flexibility, encoding multiple enzymes for the degradation of various fiber subtypes ✅ Trusted Source
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Xu, J.; Bjursell, M.K.; Himrod, J.; Deng, S.; Carmichael, L.K.; Chiang, H.C.; Hooper, L.V.; Gordon, J.I. A Genomic View of the Human-Bacteroides thetaiotaomicron Symbiosis. Science 2003, 299, 2074–2076.
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Carbohydrate-active enzymes (CAZymes), including glycoside hydrolases, polysaccharide lysases, and carbohydrate esterases, play pivotal roles in fermentation reactions ✅ Trusted Source
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Lombard, V.; Ramulu, H.G.; Drula, E.; Coutinho, P.M.; Henrissat, B. The carbohydrate-active enzymes database (CAZy) in 2013. Nucleic Acids Res. 2014, 42, D490–D495.
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Hamaker, B.R.; Tuncil, Y.E. A Perspective on the Complexity of Dietary Fiber Structures and Their Potential Effect on the Gut Microbiota. J. Mol. Biol. 2014, 426, 3838–3850.
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Compositional differences among resistant starches can have distinct effects on the host microbiota.
In humans, RS4 consumption increased Actinobacteria and Bacteroidetes abundance while reducing Firmicutes ✅ Trusted Source
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Martínez, I.; Kim, J.; Duffy, P.R.; Schlegel, V.L.; Walter, J. Resistant Starches Types 2 and 4 Have Differential Effects on the Composition of the Fecal Microbiota in Human Subject. PLoS ONE 2010, 5, e15046.
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RS4 also led to higher levels of Parabacteroides distasonis and Bifidobacterium asolescentis.
On the other hand, RS2 had no effect at the phylum level but increased populations of Ruminococcus bromii and Eubacterium rectale at the species level ✅ Trusted Source
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Martínez, I.; Kim, J.; Duffy, P.R.; Schlegel, V.L.; Walter, J. Resistant Starches Types 2 and 4 Have Differential Effects on the Composition of the Fecal Microbiota in Human Subject. PLoS ONE 2010, 5, e15046.
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In vitro experiments demonstrated that Ruminococcus bromii is crucial for RS2 and RS3 fermentation ✅ Trusted Source
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Ze, X.; Duncan, S.H.; Louis, P.; Flint, H.J. Ruminococcus bromii is a keystone species for the degradation of resistant starch in the human colon. ISME J. 2012, 6, 1535–1543.
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, with other colonic microbes further fermenting the products into SCFA.
Bifidobacterium breve and Bifidobacterium adolescentis were also identified as enzymes capable of degrading resistant starch ✅ Trusted Source
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Ryan, S.M.; Fitzgerald, G.F.; van Sinderen, D. Screening for and identification of starch-, amylopectin-, and pullu-lan-degrading activities in bifidobacterial strains. Appl. Environ. Microbiol. 2006, 72, 5289–5296.
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Inulin consumption in humans increased Bifidobacterium bifidum ✅ Trusted Source
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Gibson, G.R. Dietary Modulation of the Human Gut Microflora Using the Prebiotics Oligofructose and Inulin. J. Nutr. 1999, 129, 1438S–1441S.
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✅ Trusted Source
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Kruse, H.-P.; Kleessen, B.; Blaut, M. Effects of inulin on faecal bifidobacteria in human subjects. Br. J. Nutr. 1999, 82, 375–382.
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✅ Trusted Source
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Harmsen, H.J.M.; Raangs, G.C.; Franks, A.H.; Wildeboer-Veloo, A.C.M.; Welling, G.W. The Effect of the Prebiotic Inulin and the Probiotic Bifidobacterium longum on the Fecal Microflora of Healthy Volunteers Measured by FISH and DGGE. Microb. Ecol. Health Dis. 2002, 14, 212–220.
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and Faecalibacterium prausnitzii levels ✅ Trusted Source
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Ramirez-Farias, C.; Slezak, K.; Fuller, Z.; Duncan, A.; Holtrop, G.; Louis, P. Effect of inulin on the human gut microbiota: Stimulation of Bifidobacterium adolescentis and Fae-calibacterium prausnitzii. Br. J. Nutr. 2008, 101, 541–550.
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, while lowering Enterococcus species ✅ Trusted Source
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Kleessen, B.; Sykura, B.; Zunft, H.J.; Blaut, M. Effects of inulin and lactose on fecal microflora, microbial activity, and bowel habit in elderly constipated persons. Am. J. Clin. Nutr. 1997, 65, 1397–1402.
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Cross-feeding occurred, with Eubacterium rectale breaking down inulin initially, followed by fermentation of the products by Anserostipes caccae ✅ Trusted Source
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Van den Abbeele, P.; Gérard, P.; Rabot, S.; Bruneau, A.; El Aidy, S.; Derrien, M.; Kleerebezem, M.; Zoetendal, E.G.; Smidt, H.; Verstraete, W.; et al. Arabinoxylans and inulin differentially modulate the mucosal and luminal gut microbiota and mu-cin-degradation in humanized rats. Environ. Microbiol. 2011, 13, 2667–2680.
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Wheat bran supplementation increased the Firmicutes and Bacteroidetes phyla ✅ Trusted Source
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Vitaglione, P.; Mennella, I.; Ferracane, R.; Rivellese, A.A.; Giacco, R.; Ercolini, D.; Gibbons, S.M.; La Storia, A.; Gilbert, J.A.; Jonnalagadda, S.; et al. Whole-grain wheat consumption reduces inflammation in a randomized controlled trial on overweight and obese subjects with unhealthy dietary and lifestyle behaviors: Role of polyphenols bound to cereal dietary fiber. Am. J. Clin. Nutr. 2015, 101, 251–261.
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Obese men supplemented with wheat bran showed elevated levels of Actinobacteria at the genus level, including Prevotella, Bacteroides, Eggerthella, Lachnospiraceae, Corynebacterium, and Collinsella ✅ Trusted Source
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Salonen, A.H.; Lahti, L.; Salojärvi, J.; Holtrop, G.; Korpela, K.; Duncan, S.H.; Date, P.; Farquharson, F.; Johnstone, A.M.; Lobley, G.E.; et al. Impact of diet and individual variation on intestinal microbiota composition and fermentation products in obese men. ISME J. 2014, 8, 2218–2230.
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In contrast, whole-grain wheat intervention in healthy individuals increased Enterococcus, Bifidobacterium, Clostridium, and Lactobacillus ✅ Trusted Source
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Costabile, A.; Klinder, A.; Fava, F.; Napolitano, A.; Fogliano, V.; Leonard, C.; Gibson, G.R.; Tuohy, K.M. Whole-grain wheat breakfast cereal has a prebiotic effect on the human gut microbiota: A double-blind, placebo-controlled, crossover study. Br. J. Nutr. 2007, 99, 110–120.
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, indicating personalized effects based on the initial microbiome.
Oat-derived β-glucan increased Bacteroidetes and decreased Firmicutes ✅ Trusted Source
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Wang, Y.; Ames, N.P.; Tun, H.M.; Tosh, S.M.; Jones, P.J.; Khafipour, E. High Molecular Weight Barley β-Glucan Alters Gut Microbiota Toward Reduced Cardiovascular Disease Risk. Front. Microbiol. 2016, 7, 129.
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In rats, β-glucan intervention boosted Bacteroides and Prevotella species ✅ Trusted Source
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Snart, J.; Bibiloni, R.; Grayson, T.; Lay, C.; Zhang, H.; Allison, G.E.; Laverdiere, J.K.; Temelli, F.; Vasanthan, T.; Bell, R.; et al. Supplementation of the Diet with High-Viscosity Beta-Glucan Results in Enrichment for Lactobacilli in the Rat Cecum. Appl. Environ. Microbiol. 2006, 72, 1925–1931.
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It also led to higher levels of Bifidobacteria ✅ Trusted Source
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Zhao, J.; Cheung, P.C.K. Fermentation of β-Glucans Derived from Different Sources by Bifidobacteria: Evaluation of Their Bifidogenic Effect. J. Agric. Food Chem. 2011, 59, 5986–5992.
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, butyrate-producing Clostridium histolyticum ✅ Trusted Source
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Hughes, S.A.; Shewry, P.R.; Gibson, G.R.; McCleary, B.V.; Rastall, R.A. In vitro fermentation of oat and barley derived β-glucans by human faecal microbiota. FEMS Microbiol. Ecol. 2008, 64, 482–493.
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, and other Clostridium family members capable of fermenting β-glucan ✅ Trusted Source
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Zappe, H.; Jones, W.A.; Jones, D.T.; Woods, D.R. Structure of an endo-beta-1,4-glucanase gene from Clostridium aceto-butylicum P262 showing homology with endoglucanase genes from Bacillus spp. Appl. Environ. Microbiol. 1988, 54, 1289–1292.
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✅ Trusted Source
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Foong, F.; Hamamoto, T.; Shoseyov, O.; Doi, R.H. Nucleotide sequence and characteristics of endoglucanase gene engB from Clostridium cellulovorans. J. Gen. Microbiol. 1991, 137, 1729–1736.
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✅ Trusted Source
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Mittendorf, V.; Thomson, J.A. Cloning of an endo-(1→4) -glucanase gene, celA, from the rumen bacterium Clostridium sp. (‘C. longisporum’) and characterization of its product, CelA, in Escherichia coli. J. Gen. Microbiol. 1993, 139, 3233–3242.
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Gum acacia fiber increased Bifidobacteria and Lactobacilli ✅ Trusted Source
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Cherbut, C.; Michel, C.; Raison, V.; Kravtchenko, T.; Severine, M. Acacia Gum is a Bifidogenic Dietary Fibre with High Digestive Tolerance in Healthy Humans. Microb. Ecol. Health Dis. 2003, 15, 43–50. , with Prevotella ruminocola postulated as one of the main fermenters ✅ Trusted Source
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Kishimoto, A.; Ushida, K.; Phillips, G.O.; Ogasawara, T.; Sasaki, Y. Identification of Intestinal Bacteria Responsible for Fermentation of Gum Arabic in Pig Model. Curr. Microbiol. 2006, 53, 173–177.
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✅ Trusted Source
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Glover, D.A.; Ushida, K.; Phillips, A.O.; Riley, S.G. Acacia(sen) SUPERGUMTM (Gum arabic): An evaluation of potential health benefits in human subjects. Food Hydrocoll. 2009, 23, 2410–2415.
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Galacto-oligosaccharide (GOS) increased Bifidobacterium species ✅ Trusted Source
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Davis, L.M.G.; Martínez, I.; Walter, J.; Goin, C.; Hutkins, R.W. Barcoded Pyrosequencing Reveals That Consumption of Galactooligosaccharides Results in a Highly Specific Bifidogenic Response in Humans. PLoS ONE 2011, 6, e25200.
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and Faecalibacterium prausnitzii ✅ Trusted Source
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Davis, L.M.G.; Martínez, I.; Walter, J.; Goin, C.; Hutkins, R.W. Barcoded Pyrosequencing Reveals That Consumption of Galactooligosaccharides Results in a Highly Specific Bifidogenic Response in Humans. PLoS ONE 2011, 6, e25200.
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, while fructo-oligosaccharide (FOS) fermented with Bifidobacterium and Collinsella aerofaciens ✅ Trusted Source
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Cook, G.M.; Russell, J.B. Energy-spilling reactions of Streptococcus bovis and resistance of its membrane to proton conductance. Appl. Environ. Microbiol. 1994, 60, 1942–1948.
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Whole-grain barley intake increased Prevotella copri ✅ Trusted Source
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Kovatcheva-Datchary, P.; Nilsson, A.; Akrami, R.; Lee, Y.S.; De Vadder, F.; Arora, T.; Hallen, A.; Martens, E.; Björck, I.; Bäckhed, F. Dietary Fiber-Induced Improvement in Glucose Metabolism Is Associated with Increased Abundance of Prevotella. Cell Metab. 2015, 22, 971–982.
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, whereas whole-grain rye fiber had no effect on gut microbiota in healthy Danes ✅ Trusted Source
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Vuholm, S.; Nielsen, D.S.; Iversen, K.N.; Suhr, J.; Westermann, P.; Krych, L.; Andersen, J.R.; Kristensen, M. Whole-Grain Rye and Wheat Affect Some Markers of Gut Health without Altering the Fecal Microbiota in Healthy Overweight Adults: A 6-Week Randomized Trial. J. Nutr. 2017, 147, jn250647-2075.
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Interestingly, rye bread supplementation in Finnish individuals with metabolic syndrome resulted in lower Bacteroidetes levels and higher Firmicutes and Actinobacteria ✅ Trusted Source
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Lappi, J.; Salojärvi, J.; Kolehmainen, M.; Mykkänen, H.; Poutanen, K.; De Vos, W.M.; Salonen, A. Intake of Whole-Grain and Fiber-Rich Rye Bread Versus Refined Wheat Bread Does Not Differentiate Intestinal Microbiota Composition in Finnish Adults with Metabolic Syndrome. J. Nutr. 2013, 143, 648–655.
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In essence, dietary fiber profoundly affects gut microbiota composition, involving multiple species and enzymes in fiber degradation.
This intricate symbiotic relationship starts with primary degraders and ends with cross-feeders producing SCFAs ✅ Trusted Source
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Flint, H.J.; Scott, K.P.; Louis, P.; Duncan, S.H. The role of the gut microbiota in nutrition and health. Nat. Rev. Gastroenterol. Hepatol. 2012, 9, 577–589.
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✅ Trusted Source
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Koropatkin, N.M.; Cameron, E.A.; Martens, E.C. How glycan metabolism shapes the human gut microbiota. Nat. Rev. Genet. 2012, 10, 323–335.
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Although cross-feeding in resistant starch fermentation is well-documented, more research is needed to understand these relationships in the breakdown of other fiber types.
To harness the full potential of dietary fiber in treating metabolic disorders, it's essential to investigate the specific roles these microbiota play in metabolizing different fiber subtypes.
The Healthy By-products of Fiber Digestion
Dietary fiber fuels your gut's microbial community, yielding a wealth of health benefits.
It's linked to reduced cholesterol and improved glucose control ✅ Trusted Source
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O’Grady, J.; O’Connor, E.M.; Shanahan, F. Review article: Dietary fibre in the era of microbiome science. Aliment. Pharmacol. Ther. 2019, 49, 506–515.
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Fiber doesn't just influence your gut's composition; it also shapes the metabolites produced there ✅ Trusted Source
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Wong, J.M.W.; De Souza, R.; Kendall, C.W.C.; Emam, A.; Jenkins, D.J.A. Colonic Health: Fermentation and Short Chain Fatty Acids. J. Clin. Gastroenterol. 2006, 40, 235–243.
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Short-chain fatty acids (SCFAs) like butyrate, acetate, and propionate are the key players.
SCFAs impact various bodily processes, especially in the gut ✅ Trusted Source
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Makki, K.; Deehan, E.C.; Walter, J.; Bäckhed, F. The Impact of Dietary Fiber on Gut Microbiota in Host Health and Disease. Cell Host Microbe 2018, 23, 705–715.
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The type of fiber and the mix of gut microbes determine the quantity and variety of SCFAs produced ✅ Trusted Source
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Yang, J.; Martínez, I.; Walter, J.; Keshavarzian, A.; Rose, D.J. In vitro characterization of the impact of selected dietary fibers on fecal microbiota composition and short chain fatty acid production. Anaerobe 2013, 23, 74–81.
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✅ Trusted Source
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Yang, J.; Rose, D.J. Long-term dietary pattern of fecal donor correlates with butyrate production and markers of protein fermentation during in vitro fecal fermentation. Nutr. Res. 2014, 34, 749–759.
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SCFAs are usually absorbed in the colon, playing a pivotal role in supporting your health and metabolism.
Reduced fiber intake can lead to lower microbial diversity and fewer SCFAs ✅ Trusted Source
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O’Grady, J.; O’Connor, E.M.; Shanahan, F. Review article: Dietary fibre in the era of microbiome science. Aliment. Pharmacol. Ther. 2019, 49, 506–515.
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How Fiber Benefits Your Body
Dietary fiber, a key player in gut health, unleashes short-chain fatty acids (SCFAs), especially butyrate, which activate essential receptors in the digestive tract.
These receptors, including GPR41, GPR43, and GPR109A, influence vital metabolic functions like glucose and lipid regulation, as well as appetite control ✅ Trusted Source
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den Besten, G.; Van Eunen, K.; Groen, A.K.; Venema, K.; Reijngoud, D.J.; Bakker, B.M. The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism. J. Lipid Res. 2013, 54, 2325–2340.
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Butyrate and propionate, when produced by fiber fermentation, stimulate gluconeogenesis genes, promoting a feeling of fullness by enhancing hepatic portal vein glucose sensing.
Acetate, another SCFA, aids in satiety through hypothalamic signaling.
Moreover, SCFAs trigger the release of satiety-inducing peptides, PYY and GLP-1, from colon cells, helping manage appetite and digestion ✅ Trusted Source
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Delaere, F.; Duchampt, A.; Mounien, L.; Seyer, P.; Duraffourd, C.; Zitoun, C.; Thorens, B.; Mithieux, G. The role of sodium-coupled glucose co-transporter 3 in the satiety effect of portal glucose sensing. Mol. Metab. 2013, 2, 47–53.
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✅ Trusted Source
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De Vadder, F.; Kovatcheva-Datchary, P.; Goncalves, D.; Vinera, J.; Zitoun, C.; Duchampt, A.; Bäckhed, F.; Mithieux, G. Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits. Cell 2014, 156, 84–96.
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✅ Trusted Source
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Frost, G.; Sleeth, M.L.; Sahuri-Arisoylu, M.; Lizarbe, B.; Cerdan, S.; Brody, L.; Anastasovska, J.; Ghourab, S.; Hankir, M.; Zhang, S.; et al. The short-chain fatty acid acetate reduces appetite via a central homeostatic mechanism. Nat. Commun. 2014, 5, 3611.
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✅ Trusted Source
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Samuel, B.S.; Shaito, A.; Motoike, T.; Rey, F.E.; Backhed, F.; Manchester, J.K.; Hammer, R.E.; Williams, S.C.; Crowley, J.; Yanagisawa, M.; et al. Effects of the gut microbiota on host adiposity are modulated by the short-chain fatty-acid binding G pro-tein-coupled receptor, Gpr41. Proc. Natl. Acad. Sci. USA 2008, 105, 16767–16772.
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Dietary fiber, through SCFAs, indirectly affects metabolism by curbing calorie intake and promoting fullness.
Fiber’s Role in Managing Blood Sugar and Fats
Dietary Fiber's Influence on Glucose Regulation:
Research has shown that dietary fiber positively affects glucose metabolism by producing short-chain fatty acids (SCFAs) in the colon ✅ Trusted Source
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Saltiel, A.R.; Kahn, C.R. Insulin signalling and the regulation of glucose and lipid metabolism. Nat. Cell Biol. 2001, 414, 799–806.
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These SCFAs, particularly propionate and acetate, activate receptors like GPR43 and stimulate the release of GLP-1, a hormone that promotes insulin secretion and inhibits glucagon ✅ Trusted Source
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Wei, Y.; Mojsov, S. Tissue-specific expression of the human receptor for glucagon-like peptide-I: Brain, heart and pancreatic forms have the same deduced amino acid sequences. FEBS Lett. 1995, 358, 219–224.
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✅ Trusted Source
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Farilla, L.; Bulotta, A.; Hirshberg, B.; Calzi, S.L.; Khoury, N.; Noushmehr, H.; Bertolotto, C.; Di Mario, U.; Harlan, D.M.; Perfetti, R. Glucagon-Like Peptide 1 Inhibits Cell Apoptosis and Improves Glucose Responsiveness of Freshly Isolated Human Islets. Endocrinology 2003, 144, 5149–5158.
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✅ Trusted Source
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Xiong, X.; Shao, W.; Jin, T. New insight into the mechanisms underlying the function of the incretin hormone glucagon-like peptide-1 in pancreatic β-cells. Islets 2012, 4, 359–365.
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This interaction enhances insulin sensitivity and glucose tolerance.
Butyrate, another SCFA, independently induces glucose synthesis in the intestines, further improving glucose metabolism ✅ Trusted Source
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De Vadder, F.; Kovatcheva-Datchary, P.; Goncalves, D.; Vinera, J.; Zitoun, C.; Duchampt, A.; Bäckhed, F.; Mithieux, G. Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits. Cell 2014, 156, 84–96.
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✅ Trusted Source
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Gautier-Stein, A.; Zitoun, C.; Lalli, E.; Mithieux, G.; Rajas, F. Transcriptional regulation of the glucose-6-phosphatase gene by cAMP/vasoactive intestinal peptide in the intestine. Role of HNF4alpha, CREM, HNF1alpha, and C/EBPalpha. J. Biol. Chem. 2006, 281, 31268–31278. ✅ Trusted Source
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Mutel, E.; Gautier-Stein, A.; Abdul-Wahed, A.; Amigó-Correig, M.; Zitoun, C.; Stefanutti, A.; Houberdon, I.; Tourette, J.-A.; Mithieux, G.; Rajas, F. Control of Blood Glucose in the Absence of Hepatic Glucose Production During Prolonged Fasting in Mice: Induction of Renal and Intestinal Gluconeogenesis by Glucagon. Diabetes 2011, 60, 3121–3131.
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Additionally, SCFAs can reduce hepatic gluconeogenesis ✅ Trusted Source
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Deehan, E.C.; Duar, R.M.; Armet, A.M.; Perez-Munoz, M.E.; Jin, M.; Walter, J. Modulation of the Gastrointestinal Microbiome with Nondigestible Fermentable Carbohydrates to Improve Human Health. Microbiol. Spectr. 2018, 5, 453–483. , which is linked to insulin resistance and chronic gut diseases ✅ Trusted Source
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Magnusson, I.; Rothman, D.L.; Katz, L.D.; Shulman, R.G.; Shulman, G.I. Increased rate of gluconeogenesis in type II diabetes mellitus. A 13C nuclear magnetic resonance study. J. Clin. Investig. 1992, 90, 1323–1327.
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✅ Trusted Source
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Clore, J.N.; Stillman, J.; Sugerman, H. Glucose-6-phosphatase flux in vitro is increased in type 2 diabetes. Diabetes 2000, 49, 969–974.
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Dietary Fiber's Impact on Lipid Metabolism:
SCFAs from fiber fermentation also influence lipid metabolism.
They activate receptors like GPR41 and GPR43 ✅ Trusted Source
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Blundell, J.; De Graaf, C.; Hulshof, T.; Jebb, S.; Livingstone, B.; Lluch, A.; Mela, D.; Salah, S.; Schuring, E.; Van Der Knaap, H.; et al. Appetite control: Methodological aspects of the evaluation of foods. Obes. Rev. 2010, 11, 251–270.
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and even the key regulator PPAR-γ ✅ Trusted Source
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den Besten, G.; Bleeker, A.; Gerding, A.; Van Eunen, K.; Havinga, R.; Van Dijk, T.H.; Oosterveer, M.H.; Jonker, J.W.; Groen, A.K.; Reijngoud, D.-J.; et al. Short-Chain Fatty Acids Protect Against High-Fat Diet–Induced Obesity via a PPARgamma-Dependent Switch from Lipogenesis to Fat Oxidation. Diabetes 2015, 64, 2398–2408.
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Acetate can be used in the liver for lipogenesis ✅ Trusted Source
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Wong, J.M.W.; De Souza, R.; Kendall, C.W.C.; Emam, A.; Jenkins, D.J.A. Colonic Health: Fermentation and Short Chain Fatty Acids. J. Clin. Gastroenterol. 2006, 40, 235–243.
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, while propionate enhances adipose tissue lipoprotein lipase activity ✅ Trusted Source
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Ge, H.; Li, X.; Weiszmann, J.; Wang, P.; Baribault, H.; Chen, J.-L.; Tian, H.; Li, Y. Activation of G Protein-Coupled Receptor 43 in Adipocytes Leads to Inhibition of Lipolysis and Suppression of Plasma Free Fatty Acids. Endocrinology 2008, 149, 4519–4526.
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✅ Trusted Source
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Al-Lahham, S.; Roelofsen, H.; Rezaee, F.; Weening, D.; Hoek, A.; Vonk, R.; Venema, K. Propionic acid affects immune status and metabolism in adipose tissue from overweight subjects. Eur. J. Clin. Investig. 2011, 42, 357–364.
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Studies have shown that SCFA administration improves metabolic parameters, including fat oxidation and energy expenditure ✅ Trusted Source
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Canfora, E.E.; Van Der Beek, C.M.; Jocken, J.W.E.; Goossens, G.; Holst, J.J.; Damink, S.W.M.O.; Lenaerts, K.; DeJong, C.H.C.; Blaak, E.E. Colonic infusions of short-chain fatty acid mixtures promote energy metabolism in overweight/obese men: A randomized crossover trial. Sci. Rep. 2017, 7, 1–12.
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Resistant Starch (RS) and Glucose Regulation:
Studies on RS, a type of dietary fiber, have yielded mixed results ✅ Trusted Source
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Sharma, A.; Yadav, B.S. Ritika Resistant Starch: Physiological Roles and Food Applications. Food Rev. Int. 2008, 24, 193–234.
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✅ Trusted Source
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Fuentes-Zaragoza, E.; Riquelme-Navarrete, M.; Sánchez-Zapata, E.; Pérez-Álvarez, J. Resistant starch as functional ingredient: A review. Food Res. Int. 2010, 43, 931–942.
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While some research showed improvements in insulin sensitivity and reductions in visceral fat and cholesterol levels ✅ Trusted Source
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Johnston, K.L.; Thomas, E.L.; Bell, J.D.; Frost, G.S.; Robertson, M.D. Resistant starch improves insulin sensitivity in metabolic syndrome. Diabet. Med. 2010, 27, 391–397.
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, other studies found no significant effects ✅ Trusted Source
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Bodinham, C.L.; Frost, G.S.; Robertson, M.D. Acute ingestion of resistant starch reduces food intake in healthy adults. Br. J. Nutr. 2009, 103, 917–922.
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Arabinoxylan, another fiber type, has been linked to lower postprandial glucose and insulin levels, especially in patients with type 2 diabetes ✅ Trusted Source
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Lu, Z.X.; Walker, K.Z.; Muir, J.G.; Mascara, T.; O’Dea, K. Arabinoxylan fiber, a byproduct of wheat flour processing, reduces the postprandial glucose response in normoglycemic subjects. Am. J. Clin. Nutr. 2000, 71, 1123–1128.
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✅ Trusted Source
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Lu, Z.X.; Walker, K.Z.; Muir, J.G.; O’Dea, K. Arabinoxylan fibre improves metabolic control in people with Type II diabetes. Eur. J. Clin. Nutr. 2004, 58, 621–628.
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✅ Trusted Source
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Kjølbæk, L.; Benítez-Páez, A.; del Pulgar, E.M.G.; Brahe, L.K.; Liebisch, G.; Matysik, S.; Rampelli, S.; Vermeiren, J.; Brigidi, P.; Larsen, L.H.; et al. Arabinoxylan oligosaccharides and polyunsaturated fatty acid effects on gut microbiota and metabolic markers in overweight individuals with signs of metabolic syndrome: A randomized cross-over trial. Clin. Nutr. 2020, 39, 67–79.
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Gum Fibers and Glucose Control:
Gum fibers have demonstrated the ability to reduce fasting blood glucose levels and insulin release ✅ Trusted Source
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Ali, B.H.; Ziada, A.; Blunden, G. Biological effects of gum arabic: A review of some recent research. Food Chem. Toxicol. 2009, 47, 1–8.
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Their viscosity helps bind bile acids, reducing glucose absorption in the intestines ✅ Trusted Source
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Yoon, S.-J.; Chu, D.-C.; Juneja, L.R. Physiological Functions of Partially Hydrolyzed Guar Gum. J. Clin. Biochem. Nutr. 2006, 39, 134–144.
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Papathanasopoulos, A.; Camilleri, M. Dietary Fiber Supplements: Effects in Obesity and Metabolic Syndrome and Rela-tionship to Gastrointestinal Functions. Gastroenterology 2010, 138, 65–72.e2.
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Gum guar, for instance, reduced plasma fatty acids, HbA1c, and waist circumference in type 2 diabetes patients ✅ Trusted Source
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Dall’Alba, V.; Silva, F.M.; Antonio, J.P.; Steemburgo, T.; Royer, C.P.; Almeida, J.C.; Gross, J.L.; Azevedo, M.J. Improvement of the metabolic syndrome profile by soluble fibre–guar gum–in patients with type 2 diabetes: A randomised clinical trial. Br. J. Nutr. 2013, 110, 1601–1610.
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Galactooligosaccharides (GOS), Fructooligosaccharides (FOS), and Inulin:
These fiber types have shown potential in altering glucose and lipid metabolism ✅ Trusted Source
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Macfarlane, G.T.; Steed, H.; Macfarlane, S. Bacterial metabolism and health-related effects of galacto-oligosaccharides and other prebiotics. J. Appl. Microbiol. 2007, 104, 305–344.
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✅ Trusted Source
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Liu, F.; Li, P.; Chen, M.; Luo, Y.; Prabhakar, M.; Zheng, H.; He, Y.; Qi, Q.; Long, H.; Zhang, Y.; et al. Fructooligosaccharide (FOS) and Galactooligosaccharide (GOS) Increase Bifidobacterium but Reduce Butyrate Producing Bacteria with Adverse Glycemic Metabolism in healthy young population. Sci. Rep. 2017, 7, 1–12.
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However, the results vary depending on the study design ✅ Trusted Source
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Sabater-Molina, M.; Larqué, E.; Torrella, F.; Zamora, S. Dietary fructooligosaccharides and potential benefits on health. J. Physiol. Biochem. 2009, 65, 315–328.
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Costa, G.T.; Guimarães, S.B.; Sampaio, H.A.D.C. Fructo-oligosaccharide effects on blood glucose: An overview. Acta Cir. Bras. 2012, 27, 279–282.
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Inulin, in particular, has been associated with reduced circulating triacylglycerides ✅ Trusted Source
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Brighenti, F. Dietary Fructans and Serum Triacylglycerols: A Meta-Analysis of Randomized Controlled Trials. J. Nutr. 2007, 137, 2552S–2556S.
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and improved glucose metabolism ✅ Trusted Source
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Cani, P.D.; Knauf, C.; Iglesias, M.A.; Drucker, D.J.; Delzenne, N.M.; Burcelin, R. Improvement of glucose tolerance and hepatic insulin sensitivity by oligofructose requires a functional glu-cagon-like peptide 1 receptor. Diabetes 2006, 55, 1484–1490.
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Beta-Glucans and Their Impact:
Beta-glucans are known for their benefits in obesity, metabolic syndrome, type 2 diabetes, and cardiovascular disease ✅ Trusted Source
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Bozbulut, R.; Sanlier, N. Promising effects of β-glucans on glyceamic control in diabetes. Trends Food Sci. Technol. 2019, 83, 159–166.
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They have consistently been shown to reduce cholesterol and triacylglycerides ✅ Trusted Source
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Kerckhoffs, D.A.; Hornstra, G.; Mensink, R.P. Cholesterol-lowering effect of β-glucan from oat bran in mildly hypercho-lesterolemic subjects may decrease when β-glucan is incorporated into bread and cookies. Am. J. Clin. Nutr. 2003, 78, 221–227.
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Maki, K.C.; Shinnick, F.; Seeley, M.A.; Veith, P.E.; Quinn, L.C.; Hallissey, P.J.; Temer, A.; Davidson, M.H. Food Products Containing Free Tall Oil-Based Phytosterols and Oat β-Glucan Lower Serum Total and LDL Cholesterol in Hypercholesterolemic Adults. J. Nutr. 2003, 133, 808–813.
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Daou, C.; Zhang, H. Oat Beta-Glucan: Its Role in Health Promotion and Prevention of Diseases. Compr. Rev. Food Sci. Food Saf. 2012, 11, 355–365.
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✅ Trusted Source
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Whitehead, A.; Beck, E.J.; Tosh, S.; Wolever, T.M.S. Cholesterol-lowering effects of oat β-glucan: A meta-analysis of randomized controlled trials. Am. J. Clin. Nutr. 2014, 100, 1413–1421.
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Oat-derived beta-glucans, with their bile acid-binding capacity, also improve glucose metabolism ✅ Trusted Source
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Wood, P.J.; Beer, M.U.; Butler, G.B. Evaluation of role of concentration and molecular weight of oat β-glucan in determining effect of viscosity on plasma glucose and insulin following an oral glucose load. Br. J. Nutr. 2000, 84, 19–23.
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✅ Trusted Source
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Behall, K.M.; Scholfield, D.J.; Hallfrisch, J.G. Barley β-glucan reduces plasma glucose and insulin responses compared with resistant starch in men. Nutr. Res. 2006, 26, 644–650.
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Rye Fiber's Positive Effects:
Rye-based products have been found to reduce hunger ✅ Trusted Source
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Isaksson, H.; Sundberg, B.; Åman, P.; Fredriksson, H.; Olsson, J. Whole grain rye porridge breakfast improves satiety com-pared to refined wheat bread breakfast. Food Nutr. Res. 2008, 52, 1809.
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Isaksson, H.; Rakha, A.; Andersson, R.; Fredriksson, H.; Olsson, J.; Åman, P. Rye kernel breakfast increases satiety in the afternoon—An effect of food structure. Nutr. J. 2011, 10, 31.
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✅ Trusted Source
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Johansson, D.P.; Lee, I.; Risérus, U.; Langton, M.; Landberg, R. Effects of Unfermented and Fermented Whole Grain Rye Crisp Breads Served as Part of a Standardized Breakfast, on Appetite and Postprandial Glucose and Insulin Responses: A Randomized Cross-over Trial. PLoS ONE 2015, 10, e0122241.
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, postprandial glucose, insulin levels ✅ Trusted Source
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Lee, I.; Shi, L.; Webb, D.-L.; Hellström, P.M.; Risérus, U.; Landberg, R. Effects of whole-grain rye porridge with added inulin and wheat gluten on appetite, gut fermentation and postprandial glucose metabolism: A randomised, cross-over, breakfast study. Br. J. Nutr. 2016, 116, 2139–2149.
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, and cholesterol ✅ Trusted Source
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Jonsson, K.; Andersson, R.; Knudsen, K.E.; Hallmans, G.; Hanhineva, K.; Katina, K.; Kolehmainen, M.; Kyrø, C.; Langton, M.; Nordlund, E.; et al. Rye and health—Where do we stand and where do we go? Trends Food Sci. Technol. 2018, 79, 78–87.
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They have a role in managing metabolic syndrome and improving cardiovascular health.
Fiber, Obesity, and Diabetes
The Impact of Dietary Fiber on Obesity:
High dietary fiber intake correlates with increased gut microbiota diversity and lower long-term weight gain ✅ Trusted Source
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Mozaffarian, D.; Hao, T.; Rimm, E.B.; Willett, W.C.; Hu, F.B. Changes in Diet and Lifestyle and Long-Term Weight Gain in Women and Men. N. Engl. J. Med. 2011, 364, 2392–2404.
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✅ Trusted Source
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Menni, C.; Jackson, M.A.; Pallister, T.; Steves, C.J.; Spector, T.D.; Valdes, A.M. Gut microbiome diversity and high-fibre intake are related to lower long-term weight gain. Int. J. Obes. 2017, 41, 1099–1105.
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Reduced microbial diversity is associated with obesity, often reflecting lower fiber consumption ✅ Trusted Source
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Conterno, L.; Fava, F.; Viola, R.; Tuohy, K.M. Obesity and the gut microbiota: Does up-regulating colonic fermentation protect against obesity and metabolic disease? Genes Nutr. 2011, 6, 241–260.
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Dietary fiber demonstrates anti-obesity effects ✅ Trusted Source
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Adam, C.L.; Thomson, L.M.; Williams, P.A.; Ross, A.W. Soluble Fermentable Dietary Fibre (Pectin) Decreases Caloric Intake, Adiposity and Lipidaemia in High-Fat Diet-Induced Obese Rats. PLoS ONE 2015, 10, e0140392.
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✅ Trusted Source
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Moyano, G.; Sáyago-Ayerdi, S.G.; Largo, C.; Caz, V.; Santamaria, M.; Tabernero, M. Potential use of dietary fibre from Hibiscus sabdariffa and Agave tequilana in obesity management. J. Funct. Foods 2016, 21, 1–9.
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, making it a vital component in the battle against this condition.
Studies reveal that gut microbial changes play a significant role in obesity ✅ Trusted Source
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Ley, R.E.; Bäckhed, F.; Turnbaugh, P.; Lozupone, C.A.; Knight, R.D.; Gordon, J.I. Obesity alters gut microbial ecology. Proc. Natl. Acad. Sci. USA 2005, 102, 11070–11075.
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✅ Trusted Source
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Ley, R.E.; Turnbaugh, P.J.; Klein, S.; Gordon, J.I. Human gut microbes associated with obesity. Nat. Cell Biol. 2006, 444, 1022–1023.
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For instance, obese individuals exhibit lower proportions of Bacteroidetes phyla compared to lean individuals.
However, weight loss through low-calorie diets can increase Bacteroidetes abundance ✅ Trusted Source
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Ley, R.E.; Turnbaugh, P.J.; Klein, S.; Gordon, J.I. Human gut microbes associated with obesity. Nat. Cell Biol. 2006, 444, 1022–1023.
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Research also demonstrates that gut microbes contribute to increased nutrient utilization and adiposity, further underscoring their role in obesity development ✅ Trusted Source
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Turnbaugh, P.J.; Ley, R.E.; Mahowald, M.A.; Magrini, V.; Mardis, E.R.; Gordon, J.I. An obesity-associated gut microbiome with increased capacity for energy harvest. Nat. Cell Biol. 2006, 444, 1027–1031.
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The transfer of gut microbiota from healthy to germ-free mice increases body weight and promotes insulin resistance ✅ Trusted Source
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Backhed, F.; Ding, H.; Wang, T.; Hooper, L.V.; Koh, G.Y.; Nagy, A.; Semenkovich, C.F.; Gordon, J.I. The gut microbiota as an environmental factor that regulates fat storage. Proc. Natl. Acad. Sci. USA 2004, 101, 15718–15723.
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, highlighting the influence of the human gut microbiome on metabolic outcomes.
These findings are reinforced by experiments showing that colonizing mice with "obese microbiota" significantly increases body fat compared to those colonized with "lean microbiota."
Differences in the core microbiota between obese and lean individuals underscore the role of gut microbiota alterations in obesity ✅ Trusted Source
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Turnbaugh, P.J.; Hamady, M.; Yatsunenko, T.; Cantarel, B.L.; Duncan, A.; Ley, R.E.; Sogin, M.L.; Jones, W.J.; Roe, B.A.; Affourtit, J.P.; et al. A core gut microbiome in obese and lean twins. Nat. Cell Biol. 2008, 457, 480–484.
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Specific Microbes and Obesity:
At the species level, certain microbes have been associated with obesity and metabolic syndrome.
For instance, Lactobacillus has been linked to obesity, with obese individuals having a higher abundance of this bacterial genus ✅ Trusted Source
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Armougom, F.; Henry, M.; Vialettes, B.; Raccah, D.; Raoult, D. Monitoring Bacterial Community of Human Gut Microbiota Reveals an Increase in Lactobacillus in Obese Patients and Methanogens in Anorexic Patients. PLoS ONE 2009, 4, e7125.
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However, in obese children, Faecalibacterium prausnitzii was found to be more abundant [ 210].
Meanwhile, germ-free mice colonized with Bacteroides thetaiotaomicron exhibited a 23% increase in body fat composition ✅ Trusted Source
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Backhed, F.; Ding, H.; Wang, T.; Hooper, L.V.; Koh, G.Y.; Nagy, A.; Semenkovich, C.F.; Gordon, J.I. The gut microbiota as an environmental factor that regulates fat storage. Proc. Natl. Acad. Sci. USA 2004, 101, 15718–15723.
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Other studies have identified correlations between specific microbial populations and obesity risk, with variations in Clostridium histolyticum, Eubacterium rectale, Clostridium coccoides, and the Bacteroides/Prevotella group among obese individuals ✅ Trusted Source
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Kalliomäki, M.; Collado, M.C.; Salminen, S.; Isolauri, E. Early differences in fecal microbiota composition in children may predict overweight. Am. J. Clin. Nutr. 2008, 87, 534–538.
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Lipopolysaccharide (LPS)-producing microbes have also been implicated in obesity, with obese individuals showing significantly higher circulating LPS concentrations ✅ Trusted Source
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Cani, P.D.; Knauf, C.; Iglesias, M.A.; Drucker, D.J.; Delzenne, N.M.; Burcelin, R. Improvement of glucose tolerance and hepatic insulin sensitivity by oligofructose requires a functional glu-cagon-like peptide 1 receptor. Diabetes 2006, 55, 1484–1490.
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✅ Trusted Source
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Cani, P.; Bibiloni, R.; Knauf, C.; Waget, A.; Neyrinck, A.M.; Delzenne, N.M.; Burcelin, R. Changes in Gut Microbiota Control Metabolic Endotoxemia-Induced Inflammation in High-Fat Diet-Induced Obesity and Diabetes in Mice. Diabetes 2008, 57, 1470–1481.
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The Role of Dietary Fiber in Shaping Microbiota:
Dietary fiber interventions may offer a promising strategy to address obesity.
Differences in gut microbiota composition between obese and lean individuals ✅ Trusted Source
➤ Go to source
Davis, H.C. Can the gastrointestinal microbiota be modulated by dietary fibre to treat obesity? Ir. J. Med. Sci. 2017, 187, 393–402.
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are similar to those observed between individuals consuming high-fiber and low-fiber diets ✅ Trusted Source
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De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696.
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This correlation strengthens the hypothesis that dietary fiber can influence obesity through its impact on gut microbiota.
Obesity, T2DM, and Gut Microbiota:
T2DM is closely associated with obesity and metabolic syndrome.
Over 80% of T2DM individuals are overweight or obese, and increased weight gain is a major risk factor for T2DM development ✅ Trusted Source
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Patterson, E.; Ryan, P.M.; Cryan, J.F.; Dinan, T.G.; Ross, R.P.; Fitzgerald, G.F.; Stanton, C. Gut microbiota, obesity and diabetes. Postgrad. Med. J. 2016, 92, 286–300.
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Studies have revealed significant alterations in the gut microbiota of individuals with T2DM.
These alterations include a lower abundance of beneficial butyrate-producing microbes and a higher prevalence of pathogenic bacteria ✅ Trusted Source
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Qin, J.; Li, Y.; Cai, Z.; Li, S.; Zhu, J.; Zhang, F.; Liang, S.; Zhang, W.; Guan, Y.; Shen, D.; et al. A metagenome-wide association study of gut microbiota in type 2 diabetes. Nature 2012, 490, 55–60.
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The impact of metformin, a commonly prescribed T2DM medication, on gut microbiota further underscores the role of gut microbes in T2DM ✅ Trusted Source
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Zhao, L.; Lou, H.; Peng, Y.; Chen, S.; Zhang, Y.; Li, X. Comprehensive relationships between gut microbiome and faecal metabolome in individuals with type 2 diabetes and its complications. Endocrine 2019, 66, 526–537.
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✅ Trusted Source
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Forslund, K.; Hildebrand, F.; Nielsen, T.R.; Falony, G.; Le Chatelier, E.; Sunagawa, S.; Prifti, E.; Vieira-Silva, S.; Gudmundsdottir, V.; Pedersen, H.K.; et al. Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota. Nature 2015, 528, 262–266.
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While the exact mechanisms remain unclear ✅ Trusted Source
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Brunkwall, L.; Orho-Melander, M. The gut microbiome as a target for prevention and treatment of hyperglycaemia in type 2 diabetes: From current human evidence to future possibilities. Diabetologia 2017, 60, 943–951.
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, it appears that metformin's effects are mediated through the gut microbiota.
Individuals with obesity and T2DM experience shifts in their gut microbiota, contributing to their disease phenotype ✅ Trusted Source
➤ Go to source
Ley, R.E.; Bäckhed, F.; Turnbaugh, P.; Lozupone, C.A.; Knight, R.D.; Gordon, J.I. Obesity alters gut microbial ecology. Proc. Natl. Acad. Sci. USA 2005, 102, 11070–11075.
➤ Get "Smart Citations"
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✅ Trusted Source
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Wu, X.; Ma, C.; Han, L.; Nawaz, M.; Gao, F.; Zhang, X.; Yu, P.; Zhao, C.; Li, L.; Zhou, A.; et al. Molecular Characterisation of the Faecal Microbiota in Patients with Type II Diabetes. Curr. Microbiol. 2010, 61, 69–78.
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Dietary Fiber as a Therapeutic Approach:
Dietary fiber has the potential to modulate the gut microbiota, creating an environment conducive to the growth of beneficial short-chain fatty acid (SCFA)-producing microbes while improving glucose and lipid metabolism.
This underscores its importance as a potential therapeutic approach for individuals grappling with metabolic challenges.
Conclusion
Historical Dietary Changes and Metabolic Health:
In recent centuries, dietary shifts contributed to differing metabolic disease rates in developed and developing nations.
The Western diet, rich in high-glycemic load, low-fiber foods, contrasts with our ancestors' 100-gram daily fiber intake ✅ Trusted Source
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Eaton, S.B. The ancestral human diet: What was it and should it be a paradigm for contemporary nutrition? Proc. Nutr. Soc. 2006, 65, 1–6.
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Nowadays, non-industrialized nations average 50 grams ✅ Trusted Source
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O’Keefe, S.J.D.; Li, J.V.; Lahti, L.; Ou, J.; Carbonero, F.; Mohammed, K.; Posma, J.M.; Kinross, J.; Wahl, E.; Ruder, E.; et al. Fat, fibre and cancer risk in African Americans and rural Africans. Nat. Commun. 2015, 6, 1–14.
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, while Western industrialized nations typically consume only 12–18 grams daily ✅ Trusted Source
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Slavin, J.L. Position of the American Dietetic Association: Health implications of dietary fiber. J. Am. Diet. Assoc. 2008, 108, 1716–1731. ✅ Trusted Source
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Jew, S.; AbuMweis, S.S.; Jones, P.J. Evolution of the Human Diet: Linking Our Ancestral Diet to Modern Functional Foods as a Means of Chronic Disease Prevention. J. Med. Food 2009, 12, 925–934.
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✅ Trusted Source
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Deehan, E.C.; Walter, J. The Fiber Gap and the Disappearing Gut Microbiome: Implications for Human Nutrition. Trends Endocrinol. Metab. 2016, 27, 239–242.
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This fiber gap, along with high protein and fat intake, correlates with gut microbiota differences ✅ Trusted Source
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De Filippo, C.; Cavalieri, D.; Di Paola, M.; Ramazzotti, M.; Poullet, J.B.; Massart, S.; Collini, S.; Pieraccini, G.; Lionetti, P. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl. Acad. Sci. USA 2010, 107, 14691–14696.
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✅ Trusted Source
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Martínez, I.; Stegen, J.C.; Maldonado-Gómez, M.X.; Eren, A.M.; Siba, P.M.; Greenhill, A.R.; Walter, J. The Gut Microbiota of Rural Papua New Guineans: Composition, Diversity Patterns, and Ecological Processes. Cell Rep. 2015, 11, 527–538.
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✅ Trusted Source
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De Filippo, C.; Di Paola, M.; Ramazzotti, M.; Albanese, D.; Pieraccini, G.; Banci, E.; Miglietta, F.; Cavalieri, D.; Lionetti, P. Diet, Environments, and Gut Microbiota. A Preliminary Investigation in Children Living in Rural and Urban Burkina Faso and Italy. Front. Microbiol. 2017, 8, 1979.
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Western countries' microbiomes exhibit minimal variation ✅ Trusted Source
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Arumugam, M.; Raes, J.; Pelletier, E.; Le Paslier, D.; Yamada, T.; Mende, D.R.; Fernandes, G.R.; Tap, J.; Bruls, T.; Batto, J.M.; et al. Enterotypes of the human gut microbiome. Nature 2011, 473, 174–180.
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, but vegan/vegetarian diets resemble non-industrialized populations with higher fiber intake and fewer metabolic diseases ✅ Trusted Source
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David, L.A.; Maurice, C.F.; Carmody, R.N.; Gootenberg, D.B.; Button, J.E.; Wolfe, B.E.; Ling, A.V.; Devlin, A.S.; Varma, Y.; Fischbach, M.A.; et al. Diet rapidly and reproducibly alters the human gut microbiome. Nat. Cell Biol. 2014, 505, 559–563.
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Current fiber recommendations are 30-35 grams for males and 25-32 grams for females ✅ Trusted Source
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Stephen, A.M.; Champ, M.M.-J.; Cloran, S.J.; Fleith, M.; Van Lieshout, L.; Mejborn, H.; Burley, V.J. Dietary fibre in Europe: Current state of knowledge on definitions, sources, recommendations, intakes and relationships to health. Nutr. Res. Rev. 2017, 30, 149–190.
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, but Western societies fall short.
Dietary Fiber and Metabolic Health:
Dietary fiber plays a pivotal role in improving metabolic health in individuals with obesity, metabolic syndrome, and gut-related disorders ✅ Trusted Source
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Brighenti, F. Dietary Fructans and Serum Triacylglycerols: A Meta-Analysis of Randomized Controlled Trials. J. Nutr. 2007, 137, 2552S–2556S.
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Cani, P.D.; Possemiers, S.; Van De Wiele, T.; Guiot, Y.; Everard, A.; Rottier, O.; Geurts, L.; Naslain, D.; Neyrinck, A.; Lambert, D.M.; et al. Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability. Gut 2009, 58, 1091–1103.
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Sonnenburg, J.L.; Bäckhed, F. Diet–microbiota interactions as moderators of human metabolism. Nat. Cell Biol. 2016, 535, 56–64.
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Numerous studies link dietary fiber intake to overall health ✅ Trusted Source
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Ning, H.; Van Horn, L.; Shay, C.M.; Lloyd-Jones, D.M. Associations of Dietary Fiber Intake with Long-Term Predicted Cardiovascular Disease Risk and C-Reactive Protein Levels (from the National Health and Nutrition Examination Survey Data (2005–2010)). Am. J. Cardiol. 2014, 113, 287–291.
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Livingston, K.A.; Chung, M.; Sawicki, C.M.; Lyle, B.J.; Wang, D.D.; Roberts, S.B.; McKeown, N.M. Development of a Publicly Available, Comprehensive Database of Fiber and Health Outcomes: Rationale and Methods. PLoS ONE 2016, 11, e0156961.
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, with some inconsistencies ✅ Trusted Source
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Livingston, K.A.; Chung, M.; Sawicki, C.M.; Lyle, B.J.; Wang, D.D.; Roberts, S.B.; McKeown, N.M. Development of a Publicly Available, Comprehensive Database of Fiber and Health Outcomes: Rationale and Methods. PLoS ONE 2016, 11, e0156961.
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Varying fiber amounts among studies result in diverse gut microbiota and metabolic changes, compounded by individual microbiome variations.
The highly personalized human gut microbiome complicates interventions, as some individuals lack the necessary microbiota for specific fiber breakdown.
The Need for Personalization:
A personalized approach may be necessary for addressing global metabolic health issues, potentially requiring higher fiber doses as seen in non-industrialized nations (50 grams) ✅ Trusted Source
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O’Keefe, S.J.D.; Li, J.V.; Lahti, L.; Ou, J.; Carbonero, F.; Mohammed, K.; Posma, J.M.; Kinross, J.; Wahl, E.; Ruder, E.; et al. Fat, fibre and cancer risk in African Americans and rural Africans. Nat. Commun. 2015, 6, 1–14.
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Specific fiber types like resistant starch, arabinoxylan, and gum acacia show better tolerance at higher doses.
Gradual fiber intake increases may enhance adaptability ✅ Trusted Source
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Deehan, E.C.; Walter, J. The Fiber Gap and the Disappearing Gut Microbiome: Implications for Human Nutrition. Trends Endocrinol. Metab. 2016, 27, 239–242.
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Challenges and Potential Solutions:
Dietary fiber interventions alone may not suffice to reverse metabolic issues.
Studies with germ-free mice suggest that certain beneficial microbiota may not be hereditary ✅ Trusted Source
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Sonnenburg, J.L.; Bäckhed, F. Diet–microbiota interactions as moderators of human metabolism. Nat. Cell Biol. 2016, 535, 56–64.
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A low-fiber diet can alter the microbiome within three generations, potentially irreversibly.
Combining dietary fiber with fecal microbial transplantation could introduce efficient fiber-digesting bacteria for more effective treatment.
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