Cited by 441Gut microbiota and healthGastrointestinal motility and disordersMicrobial Metabolites in Food Biotechnology

Review article: insights into colonic protein fermentation, its modulation and potential health implications

Open access
Yao, C. K., Muir, J. G., Gibson, P. R.·2016·Alimentary Pharmacology & Therapeutics

Abstract

Summary: Background: Beneficial effects of carbohydrate fermentation on gastrointestinal health are well established. Conversely, protein fermentation generates harmful metabolites but their relevance to gastrointestinal health is poorly understood. Aim: To review the effects of increased protein fermentation on biomarkers of colonic health, factors influencing fermentative activity and potential for dietary modulation to minimise detrimental effects. Methods: A literature search was performed in PubMed, Medline, EMBASE and Google scholar for clinical and pre‐clinical studies using search terms – ‘dietary protein’, ‘fermentation’, ‘putrefaction’, ‘phenols’, ‘sulphide’, ‘branched‐chain fatty acid’, ‘carbohydrate fermentation’, ‘gastrointestinal’. Results: High protein, reduced carbohydrate diets alter the colonic microbiome, favouring a potentially pathogenic and pro‐inflammatory microbiota profile, decreased short‐chain fatty acid production and increased ammonia, phenols and hydrogen sulphide concentrations. These metabolites largely compromise the colonic epithelium structure, causing mucosal inflammation but may also directly modulate the enteric nervous system and intestinal motility. Increased protein fermentation as a result of a high‐protein intake can be attenuated by addition of oligosaccharides, resistant starch and nonstarch polysaccharides and a reduction in total protein or specifically, aromatic and sulphur‐containing amino acids. These factors may have clinical importance as novel therapeutic approaches to problems, in which protein fermentation may be implicated, such as malodorous flatus, irritable bowel syndrome, ulcerative colitis and prevention of colorectal cancer. Conclusions: The direct clinical relevance of excessive protein fermentation in the pathogenesis of irritable bowel syndrome, malodorous flatus and ulcerative colitis are underexplored. Manipulating dietary carbohydrate and protein intake have potential therapeutic applications in such settings and warrant further clinical studies.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/apt.13456

Cites

8 of 8 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Other sources of endogenous SCFAs include the breakdown of proteins by the microbiota, host metabolism of long-chain fatty acids and pyruvate into acetate, and the consumption of alcohol.

    “Other sources of endogenous SCFAs include the breakdown of proteins by the microbiota (Yao et al., 2016), host metabolism of long-chain fatty acids and pyruvate into acetate (Knowles et al., 1974), as well as the consumption of alcohol (Sarkola et al., 2002).”

    From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Yao et al., 2016

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Part of this paper’s reference list could not be split into single entries.

Flagged first, then by citations

Research works printed but not linked: 93

  1. Cummings JH, Macfarlane GT. The control and consequences of bacterial fermentation in the human colon. J Appl Bacteriol 1991; 70: 443-59.
  2. Chacko A, Cummings JH. Nitrogen losses from the human small bowel: obligatory losses and the effect of physical form of food. Gut 1988; 29: 809-15.
  3. Muir JG, Yeow EG. Importance of combining indigestible carbohydrate with protein sources in the diet: implications for reducing colorectal cancer risk. Proc Nutr Soc Aus 2000; 24: 196-204.
  4. Gibson JA, Sladen GE, Dawson AM. Protein absorption and ammonia production: the effects of dietary protein and removal of the colon. Br J Nutr 1976; 35: 61-5.
  5. Cummings JH, Macfarlane GT. Role of intestinal bacteria in nutrient metabolism. JPEN 1997; 21: 357-65.
  6. Gibson S, McFarlan C, Hay S, et al. Significance of microflora in proteolysis in the colon. Appl Environ Microbiol 1989; 55: 679-83.
  7. Macfarlane GT, Cummings JH, Allison C. Protein degradation by human intestinal bacteria. J Gen Microbiol 1986; 132: 1647-56.
  8. Macfarlane GT, Gibson GR, Beatty E, et al. Estimation of short-chain fatty acid production from protein by human intestinal bacteria based on branched-chain fatty acid measurements. FEMS Microbiol Lett 1992; 101: 81-8.
  9. Bone E, Tamm A, Hill M. The production of urinary phenols by gut bacteria and their possible role in the causation of large bowel cancer. Am J Clin Nutr 1976; 29: 1448-54.
  10. Cummings JH, Hill MJ, Bone ES, et al. The effect of meat protein and dietary fiber on colonic function and metabolism. II. Bacterial metabolites in feces and urine. Am J Clin Nutr 1979; 32: 2094-101.
  11. Birkett A, Muir J, Phillips J, et al. Resistant starch lowers fecal concentrations of ammonia and phenols in humans. Am J Clin Nutr 1996; 63: 766-72.
  12. Koecher KJ, Noack JA, Timm DA, et al. Estimation and interpretation of fermentation in the gut: coupling results from a 24 h batch in vitro system with fecal measurements from a Human Intervention Feeding Study using fructo-oligosaccharides, inulin, gum acacia, and pea fiber. J Agric Food Chem 2014; 62: 1332-7.
  13. Cummings JH, Pomare EW, Branch WJ, et al. Short chain fatty acids in human large intestine, portal, hepatic and venous blood. Gut 1987; 28: 1221-7.
  14. Kalantar-Zadeh K, Yao CK, Berean KB, et al. Intestinal gas capsules: a proof-of-concept demonstration. Gastroenterol 2015; in press.
  15. Suarez F, Springfield J, Levitt M. Identification of gases responsible for the odour of human flatus and evaluation of a device purported to reduce this odour. Gut 1998; 43: 100-4.
  16. Blachier F, Davila AM, Mimoun S, et al. Luminal sulfide and large intestine mucosa: friend or foe? Amino Acids 2010; 39: 335-47.
  17. Suarez F, Springfield J, Furne J, et al. Differentiation of mouth versus gut as site of origin of odoriferous breath gases after garlic ingestion. Am J Physiol 1999; 276: G425-30.
  18. Furne J, Majerus G, Lenton P, et al. Comparison of volatile sulfur compound concentrations measured with a sulfide detector vs. gas chromatography. J Dent Res 2002; 81: 140-3.
  19. Strocchi A, Furne JK, Levitt MD. A modification of the methylene blue method to measure bacterial sulfide production in feces. J Microbiol Meth 1992; 15: 75-82.
  20. Tangerman A. Measurement and biological significance of the volatile sulfur compounds hydrogen sulfide, methanethiol and dimethyl sulfide in various biological matrices. J Chromatogr B Analyt Technol Biomed Life Sci 2009; 877: 3366-77.
  21. Ryan D, Newnham ED, Prenzler PD, et al. Metabolomics as a tool for diagnosis and monitoring in coeliac disease. Metabolomics 2014; 11: 1-11.
  22. Garner CE, Smith S, de Lacy Costello B, et al. Volatile organic compounds from feces and their potential for diagnosis of gastrointestinal disease. FASEB J 2007; 21: 1675-88.
  23. Shen Q, Chen YA, Tuohy KM. A comparative in vitro investigation into the effects of cooked meats on the human faecal microbiota. Anaerobe 2010; 16: 572-7.
  24. Richardson AJ, McKain N, Wallace RJ. Ammonia production by human faecal bacteria, and the enumeration, isolation and characterization of bacteria capable of growth on peptides and amino acids. BMC Microbiol 2013; 13: 6.
  25. Wu GD, Chen J, Hoffmann C, et al. Linking long-term dietary patterns with gut microbial enterotypes. Science 2011; 334: 105-8.
  26. Brinkworth GD, Noakes M, Clifton PM, et al. Comparative effects of very low-carbohydrate, high-fat and high- carbohydrate, low-fat weight-loss diets on bowel habit and faecal short- chain fatty acids and bacterial populations. Br J Nutr 2009; 101: 1493-502.
  27. Duncan SH, Belenguer A, Holtrop G, et al. Reduced dietary intake of carbohydrates by obese subjects results in decreased concentrations of butyrate and butyrate-producing bacteria in feces. Appl Environ Microbiol 2007; 73: 1073-8.
  28. Smith EA, Macfarlane G. Dissimilatory amino acid metabolism in human colonic bacteria. Anaerobe 1997; 3: 327-37.
  29. Heo JM, Kim JC, Hansen CF, et al. Feeding a diet with decreased protein content reduces indices of protein fermentation and the incidence of postweaning diarrhea in weaned pigs challenged with an enterotoxigenic strain of Escherichia coli. J Anim Sci 2009; 87: 2833-43.
  30. Andriamihaja M, Davila A-M, Eklou- Lawson M, et al. Colon luminal content and epithelial cell Review: protein fermentation in large bowel disease 13652036, 2016, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/apt.13456, Wiley Online Library on [17/08/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License morphology are markedly modified in rats fed with a high-protein diet. Am J Physiol Gastrointest Liver Physiol 2010; 299: G1030-7.
  31. Le Leu RK, Brown IL, Hu Y, et al. Effect of dietary resistant starch and protein on colonic fermentation and intestinal tumourigenesis in rats. Carcinogenesis 2007; 28: 240-5.
  32. Lupton JR, Marchant LJ. Independent effects of fiber and protein on colonic luminal ammonia concentration. J Nutr 1989; 119: 235-41.
  33. Toden S, Bird AR, Topping DL, et al. Differential effects of dietary whey, casein and soya on colonic DNA damage and large bowel SCFA in rats fed diets low and high in resistant starch. Br J Nutr 2007; 97: 535-43.
  34. Heinritz SN, Mosenthin R, Weiss E. Use of pigs as a potential model for research into dietary modulation of the human gut microbiota. Nutr Res Rev 2013; 26: 191-209.
  35. Pieper R, Kroger S, Richter JF, et al. Fermentable fiber ameliorates fermentable protein-induced changes in microbial ecology, but not the mucosal response, in the colon of piglets. J Nutr 2012; 142: 661-7.
  36. Bingham SA, Pignatelli B, Pollock JRA, et al. Does increased endogenous formation of N-nitroso compounds in the human colon explain the association between red meat and colon cancer? Carcinogenesis 1996; 17: 515-23.
  37. Geypens B, Claus D, Evenepoel P, et al. Influence of dietary protein supplements on the formation of bacterial metabolites in the colon. Gut 1997; 41: 70-6.
  38. Silvester KR, Bingham SA, Pollock JR, et al. Effect of meat and resistant starch on fecal excretion of apparent N-nitroso compounds and ammonia from the human large bowel. Nutr Cancer 1997; 29: 13-23.
  39. Benassi-Evans B, Clifton P, Noakes M, et al. High-protein/high red meat and high-carbohydrate weight-loss diets do not differ in their effect on faecal water genotoxicity tested by use of the WIL2-NS cell line and with other biomarkers of bowel health. Mutat Res 2010; 703: 130-6.
  40. Evenepoel P, Geypens B, Luypaerts A, et al. Digestibility of cooked and raw egg protein in humans as assessed by stable isotope techniques. J Nutr 1998; 128: 1716-22.
  41. Lin H-C, Visek WJ. Colon mucosal cell damage by ammonia in rats. J Nutr 1991; 121: 887-93.
  42. Daniel M, Wisker E, Rave G, et al. Fermentation in human subjects of nonstarch polysaccharides in mixed diets, but not in a barley fiber concentrate, could be predicted by in vitro fermentation using human fecal inocula. J Nutr 1997; 127: 1981- 8.
  43. Cremin JD, Fitch MD, Fleming SE. Glucose alleviates ammonia-induced inhibition of short-chain fatty acid metabolism in rat colonic epithelial cells. Am J Physiol Gastrointest Liver Physiol 2003; 285: G105-14.
  44. Hughes R, Kurth MJ, McGilligan V, et al. Effect of colonic bacterial metabolites on caco-2 cell paracellular permeability in vitro. Nutr Cancer 2008; 60: 259-66.
  45. McCall IC, Betanzos A, Weber DA, et al. Effects of phenol on barrier function of a human intestinal epithelial cell line correlate with altered tight junction protein localization. Toxicol Appl Pharmacol 2009; 241: 61-70.
  46. Pedersen G, Brynskov J, Saermark T. Phenol toxicity and conjugation in human colonic epithelial cells. Scand J Gastroenterol 2002; 37: 74-9.
  47. Seidel ER, Haddox M, Johnson LR. Polyamines in the response to intestinal obstruction. Am J Physiol 1984; 246: G649-53.
  48. Jørgensen J, Mortensen PB. Hydrogen sulfide and colonic epithelial metabolism. Dig Dis Sci 2001; 46: 1722-32.
  49. Roediger WE, Duncan A, Kapaniris O, et al. Reducing sulfur compounds of the colon impair colonocyte nutrition: implications for ulcerative colitis. Gastroenterology 1993; 104: 802-9.
  50. Cooper CE, Brown GC. The inhibition of mitochondrial cytochrome oxidase by the gases carbon monoxide, nitric oxide, hydrogen cyanide and hydrogen sulfide: chemical mechanism and physiological significance. J Bioenerg Biomembr 2008; 40: 533-9.
  51. Roediger WEW. The colonic epithelium in ulcerative colitis: an energy-deficiency disease? Lancet 1980; 316: 712-5.
  52. Aslam M, Batten J, Florin T, et al. Hydrogen-sulfide induced damage to the colonic mucosal barrier in the rat. Gut 1992; 33: S69.
  53. Christ SU, Eisner H-D, Dusel G, et al. Antagonistic effects of sulfide and butyrate on proliferation of colonic mucosa. Dig Dis Sci 1996; 41: 2477-81.
  54. Attene-Ramos MS, Nava GM, Muellner MG, et al. DNA damage and toxicogenomic analyses of hydrogen sulfide in human intestinal epithelial FHs 74 Int cells. Environ Mol Mutagen 2010; 51: 304-14.
  55. Musch MW, Bookstein C, Xie Y, et al. SCFA increase intestinal Na absorption by induction of NHE3 in rat colon and human intestinal C2/ bbe cells. Am J Physiol Gastrointest Liver Physiol 2001; 280: G687-93.
  56. Jaskiewicz J, Zhao Y, Hawes JW, et al. Catabolism of isobutyrate by colonocytes. Arch Biochem Biophys 1996; 327: 265-70.
  57. Linden DR. Hydrogen sulfide signaling in the gastrointestinal tract. Antioxid Redox Signal 2014; 20: 818-30.
  58. Quan X, Luo H, Liu Y, et al. Hydrogen sulfide regulates the colonic motility by inhibiting both L- type calcium channels and BK Ca channels in smooth muscle cells of rat colon. PLoS ONE 2015; 10: e0121331.
  59. Symonds EL, Peiris M, Page AJ, et al. Mechanisms of activation of mouse and human enteroendocrine cells by nutrients. Gut 2015; 64: 618-26.
  60. Asano Y, Hiramoto T, Nishino R, et al. Critical role of gut microbiota in the production of biologically active, free catecholamines in the gut lumen of mice. Am J Physiol Gastrointest Liver Physiol 2012; 303: G1288-95.
  61. De Preter V, Bulteel V, Suenaert P, et al. Pouchitis, similar to active ulcerative colitis, is associated with impaired butyrate oxidation by intestinal mucosa. Inflamm Bowel Dis 2009; 15: 335-40.
  62. Miller TW, Wang EA, Gould S, et al. Hydrogen sulfide is an endogenous potentiator of T cell activation. J Biol Chem 2012; 287: 4211-21.
  63. Zhang H, Zhi L, Moochhala S, et al. Hydrogen sulfide acts as an inflammatory mediator in cecal ligation and puncture-induced sepsis in mice by upregulating the production of cytokines and chemokines via NF-jB. Am J Physiol Lung Cell Mol Physiol 2007; 292: L960-71.
  64. Zhang H, Zhi L, Moore PK, et al. Role of hydrogen sulfide in cecal ligation and puncture-induced sepsis in the mouse. Am J Physiol Lung Cell Mol Physiol 2006; 290: L1193- 201.
  65. Wallace JL, Vong L, McKnight W, et al. Endogenous and exogenous hydrogen sulfide promotes resolution of colitis in rats. Gastroenterology 2009; 137: e1.
  66. Evenepoel P, Claus D, Geypens B, et al. Evidence for impaired assimilation and increased colonic fermentation of protein, related to gastric acid suppression therapy. Aliment Pharmacol Ther 1998; 12: 1011-9.
  67. Holgate A, Read N. Relationship between small bowel transit time and absorption of a solid meal influence of metoclopramide, magnesium sulfate, and lactulose. Dig Dis Sci 1983; 28: 812-9.
  68. Lewis S, Cochrane S. Alteration of sulfate and hydrogen metabolism in the human colon by changing intestinal transit rate. Am J Gastroenterol 2007; 102: 624-33.
  69. Layer P, Keller J. Pancreatic enzymes: secretion and luminal nutrient digestion in health and disease. J Clin Gastroenterol 1999; 28: 3-10.
  70. Gaudichon C, Bos C, Morens C, et al. Ileal losses of nitrogen and amino acids in humans and their importance to the assessment of amino acid requirements. Gastroenterology 2002; 123: 50-9.
  71. Sandstr€ om B, Andersson H, Kivist€ o B, et al. Apparent small intestinal absorption of nitrogen and minerals from soy and meat-protein-based diets. A study on human ileostomy subjects. J Nutr 1986; 116: 2209-18.
  72. Van Nuenen MHMC, Venema K, van der Woude JCJ, et al. The metabolic activity of fecal microbiota from healthy individuals and patients with inflammatory bowel disease. Dig Dis Sci 2004; 49: 485-91.
  73. Evenepoel P, Claus D, Geypens B, et al. Amount and fate of egg protein escaping assimilation in the small intestine of humans. Am J Physiol 1999; 277: G935-43.
  74. Silvester KR, Cummings JH. Does digestibility of meat protein help explain large bowel cancer risk? Nutr Cancer 1995; 24: 279-88.
  75. Young VR, Pellett PL. Plant proteins in relation to human protein and amino acid nutrition. Am J Clin Nutr 1994; 59: 1203S-12S.
  76. Shan L, Molberg Ø, Parrot I, et al. Structural basis for gluten intolerance in celiac sprue. Science 2002; 297: 2275-9.
  77. Moreno FJ. Gastrointestinal digestion of food allergens: effect on their allergenicity. Biomed Pharmacother 2007; 61: 50-60.
  78. Zhang J, Hallmans G, Andersson H, et al. Effect of oat bran on plasma cholesterol and bile acid excretion in nine subjects with ileostomies. Am J Clin Nutr 1992; 56: 99-105.
  79. Zhang J-X, Lundin E, Hallmans G, et al. Effect of rye bran on excretion of bile acids, cholesterol, nitrogen, and fat in human subjects with ileostomies. Am J Clin Nutr 1994; 59: 389-94.
  80. Knudsen BKE, Wisker E, Daniel M, et al. Digestibility of energy, protein, fat and non-starch polysaccharides in mixed diets: comparative studies between man and the rat. Br J Nutr 1994; 71: 471-87.
  81. Birkett AM, Mathers JC, Jones GP, et al. Changes to the quantity and processing of starchy foods in a Western diet can increase polysaccharides escaping digestion and improve in vitro fermentation variables. Br J Nutr 2000; 84: 63-72.
  82. Magee EA, Richardson CJ, Hughes R, et al. Contribution of dietary protein to sulfide production in the large intestine: an in vitro and a controlled feeding study in humans. Am J Clin Nutr 2000; 72: 1488-94.
  83. Smith EA, Macfarlane GT. Formation of phenolic and indolic compounds by anaerobic bacteria in the human large intestine. Microb Ecol 1997; 33: 180-8.
  84. Richardson CJ, Magee EA, Cummings JH. A new method for the determination of sulphide in gastrointestinal contents and whole blood by microdistillation and ion chromatography. Clin Chim Acta 2000; 293: 115-25.
  85. Nagasawa T, Ishii T, Kumagai H, et al. d-Cysteine desulfhydrase of Escherichia coli. Eur J Biochem 1985; 153: 541-51.
  86. Gibson G, Macfarlane G, Cummings J. Occurrence of sulphate-reducing bacteria in human faeces and the relationship of dissimilatory sulphate reduction to methanogenesis in the large gut. J Appl Bacteriol 1988; 65: 103-11.
  87. Russell WR, Duncan SH, Scobbie L, et al. Major phenylpropanoid-derived metabolites in the human gut can arise from microbial fermentation of protein. Mol Nutr Food Res 2013; 57: 523-35.
  88. Govers MJAP, Gannon NJ, Dunshea FR, et al. Wheat bran affects the site of fermentation of resistant starch and luminal indexes related to colon cancer risk: a study in pigs. Gut 1999; 45: 840-7.
  89. Ling WH, Hanninen O. Shifting from a conventional diet to an uncooked vegan diet reversibly alters fecal hydrolytic activities in humans. J Nutr 1992; 122: 924-30.
  90. Cloetens L, Broekaert WF, Delaedt Y, et al. Tolerance of arabinoxylan- oligosaccharides and their prebiotic activity in healthy subjects: a randomised, placebo-controlled cross- over study. Br J Nutr 2010; 103: 703-13.
  91. Geboes KP, De Hertogh G, De Preter V, et al. The influence of inulin on the absorption of nitrogen and the production of metabolites of protein fermentation in the colon. Br J Nutr 2006; 96: 1078-86.
  92. Hughes R, Pollock JR, Bingham S. Effect of vegetables, tea, and soy on endogenous N-nitrosation, fecal ammonia, and fecal water genotoxicity during a high red meat diet in humans. Nutr Cancer 2002; 42: 70-7.
  93. Conway EJ. An absorption apparatus for the micro-determination of certain volatile substances. II. The determination of urea and ammonia in body fluids. Biochem J 1933; 27: 430-4. 136. Reinhold JG, Chung CC. Formation of artifactual ammonia in blood by action of alkali its significance for the measurement of blood ammonia. Clin Chem 1961; 7: 54-69. 137. Silvester KR, Englyst HN, Cummings JH. Ileal recovery of starch from whole diets containing resistant starch measured in vitro and fermentation of ileal effluent. Am J Clin Nutr 1995; 62: 403-11. 138. Agricultural Research Service, U.S. Department of Agriculture. USDA National Nutrient Database for Standard Reference, Release 26. Nutrient Data Laboratory Home: U.S. Department of Agriculture, 2013. 139. Matsunami M-T, Noguchi Y, Okawa Y, et al. Colonic hydrogen sulfide & induced visceral pain and referred hyperalgesia involve activation of both Ca v 3.2 and TRPA1 channels in mice. J Pharmacol Sci 2012; 119: 293-6. 140. Paturi G, Nyanhanda T, Butts CA, et al. Effects of potato fiber and potato-resistant starch on biomarkers of colonic health in rats fed diets containing red meat. J Food Sci 2012; 77: H216-23. 141. Roediger W, Babidge W. Nitric oxide effect on coloncyte metabolism: co-action of sulfides and peroxide. Mol Cell Biochem 2000; 206: 159-67. 142. Toden S, Bird AR, Topping DL, et al. Resistant starch attenuates colonic DNA damage induced by higher dietary protein in rats. Nutr Cancer 2005; 51: 45-51. 143. Toden S, Bird AR, Topping DL, et al. Dose-dependent reduction of dietary protein-induced colonocyte DNA damage by resistant starch in rats correlates more highly with caecal butyrate than with other short chain fatty acids. Cancer Biol Ther 2007; 6: 253-8.

Cited by

Sorted by citations

Authors
Yao, C. K., Muir, J. G., & Gibson, P. R.
Affiliations
The Alfred Hospital (AU)
Corresponding author
Yao, C. K.
Venue
Alimentary Pharmacology & Therapeutics
Publisher
Wiley
Published
2015-11-02
Volume
43
Issue
2
Pages
181-196
ISSN
  • 0269-2813 (ISSN-L)
  • 1365-2036
OpenAlex
W2165105782
Cited by
441
References
8
Citations by year
2026: 42 · 2025: 36 · 2024: 54 · 2023: 56 · 2022: 64 · 2021: 50 · 2020: 44 · 2019: 42 · 2018: 23 · 2017: 20 · 2016: 10
FWCI
1.71
Type
journal article
Language
en
Open access
Locations
  • Alimentary Pharmacology & Therapeutics (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Danone
  • Ferring
  • AbbVie
  • Takeda Pharmaceuticals U.S.A.
  • Pfizer
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
  • Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
Keywords
dietary protein, gut microbiota, short-chain fatty acids, hydrogen sulfide, phenolic metabolites, branched-chain fatty acids, colonic epithelium, mucosal inflammation, irritable bowel syndrome, ulcerative colitis, colorectal cancer prevention, oligosaccharides, resistant starch, non-starch polysaccharides, sulfur-containing amino acids, dietary modulation
MeSH terms
Ammonia, Colon, Diet, Dietary Carbohydrates, Dietary Proteins, Fatty Acids, Volatile, Fermentation, Humans, Colorectal Neoplasms

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review