4.7 Article

A prospective cohort analysis of gut microbial co-metabolism in Alaska Native and rural African people at high and low risk of colorectal cancer

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 111, Issue 2, Pages 406-419

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ajcn/nqz301

Keywords

colorectal cancer; gut microbiota; dietary fiber; short-chain fatty acids; butyrate; bile acids; deoxycholic acid; Alaska Native people; rural African people

Funding

  1. NIH [R01 CA135379, R01 CA204403]
  2. German Cancer Aid (Deutsche Krebshilfe) Mildred-Scheel-Scholarship [70112121]
  3. German Research Foundation (Deutsche Forschungsgemeinschaft) [338582098]
  4. Health Data Research UK Rutherford Fund Fellowship [MR/S004033/1]
  5. Medical Research Council New Investigator Grant [MR/L009803/1]
  6. European Research Council [715662]
  7. MRC [MR/P002536/1, MR/S004033/1] Funding Source: UKRI
  8. European Research Council (ERC) [715662] Funding Source: European Research Council (ERC)

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Background: Alaska Native (AN) people have the world's highest recorded incidence of sporadic colorectal cancer (CRC) (similar to 91:100,000), whereas rural African (RA) people have the lowest risk (<5:100,000). Previous data supported the hypothesis that diet affected CRC risk through its effects on the colonic microbiota that produce tumor-suppressive or -promoting metabolites. Objectives: We investigated whether differences in these metabolites may contribute to the high risk of CRC in AN people. Methods: A cross-sectional observational study assessed dietary intake from 32 AN and 21 RA healthymiddle-aged volunteers before screening colonoscopy. Analysis of fecal microbiota composition by 16S ribosomal RNA gene sequencing and fecal/urinary metabolites by H-1-NMR spectroscopy was complemented with targeted quantification of fecal SCFAs, bile acids, and functional microbial genes. Results: Adenomatous polyps were detected in 16 of 32 AN participants, but not found in RA participants. The AN diet contained higher proportions of fat and animal protein and less fiber. AN fecal microbiota showed a compositional predominance of Blautia and Lachnoclostridium, higher microbial capacity for bile acid conversion, and low abundance of some species involved in saccharolytic fermentation (e.g., Prevotellaceae, Ruminococcaceae), but no significant lack of butyrogenic bacteria. Significantly lower concentrations of tumor-suppressive butyrate (22.5 +/- 3.1 compared with 47.2 +/- 7.3 SEM mu mol/g) coincided with significantly higher concentrations of tumor-promoting deoxycholic acid (26.7 +/- 4.2 compared with 11 +/- 1.9 mu mol/g) in AN fecal samples. AN participants had lower quantities of fecal/urinary metabolites than RA participants and metabolite profiles correlated with the abundance of distinct microbial genera in feces. The main microbial andmetabolic CRC-associated markers were not significantly altered in AN participants with adenomatous polyps. Conclusions: The low-fiber, high-fat diet of ANpeople and exposure to carcinogens derived from diet or environment are associated with a tumor-promoting colonic milieu as reflected by the high rates of adenomatous polyps in AN participants.

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