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Gut Microbiota and Blood Metabolites Related to Fiber Intake and Type 2 Diabetes.
Wang, Zheng; Peters, Brandilyn A; Yu, Bing; Grove, Megan L; Wang, Tao; Xue, Xiaonan; Thyagarajan, Bharat; Daviglus, Martha L; Boerwinkle, Eric; Hu, Gang; Mossavar-Rahmani, Yasmin; Isasi, Carmen R; Knight, Rob; Burk, Robert D; Kaplan, Robert C; Qi, Qibin.
Affiliation
  • Wang Z; Department of Epidemiology and Population Health (Z.W., B.A.P., T.W., X.X., Y.M.-R., C.R.I., R.D.B., R.C.K., Q.Q.), Albert Einstein College of Medicine, Bronx, NY.
  • Peters BA; Department of Epidemiology and Population Health (Z.W., B.A.P., T.W., X.X., Y.M.-R., C.R.I., R.D.B., R.C.K., Q.Q.), Albert Einstein College of Medicine, Bronx, NY.
  • Yu B; Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston (B.Y., M.L.G., E.B.).
  • Grove ML; Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston (B.Y., M.L.G., E.B.).
  • Wang T; Department of Epidemiology and Population Health (Z.W., B.A.P., T.W., X.X., Y.M.-R., C.R.I., R.D.B., R.C.K., Q.Q.), Albert Einstein College of Medicine, Bronx, NY.
  • Xue X; Department of Epidemiology and Population Health (Z.W., B.A.P., T.W., X.X., Y.M.-R., C.R.I., R.D.B., R.C.K., Q.Q.), Albert Einstein College of Medicine, Bronx, NY.
  • Thyagarajan B; Division of Molecular Pathology and Genomics, University of Minnesota, Minneapolis, MN (B.T.).
  • Daviglus ML; Institute for Minority Health Research, University of Illinois at Chicago College of Medicine, Chicago, IL (M.L.D.).
  • Boerwinkle E; Department of Epidemiology, Human Genetics, and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston (B.Y., M.L.G., E.B.).
  • Hu G; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX (E.B.).
  • Mossavar-Rahmani Y; Chronic Disease Epidemiology Laboratory, Pennington Biomedical Research Center, Baton Rouge, LA (G.H.).
  • Isasi CR; Department of Epidemiology and Population Health (Z.W., B.A.P., T.W., X.X., Y.M.-R., C.R.I., R.D.B., R.C.K., Q.Q.), Albert Einstein College of Medicine, Bronx, NY.
  • Knight R; Department of Epidemiology and Population Health (Z.W., B.A.P., T.W., X.X., Y.M.-R., C.R.I., R.D.B., R.C.K., Q.Q.), Albert Einstein College of Medicine, Bronx, NY.
  • Burk RD; Center for Microbiome Innovation (R.K.), University of California, San Diego, La Jolla.
  • Kaplan RC; Department of Pediatrics (R.K.), University of California, San Diego, La Jolla.
  • Qi Q; Department of Epidemiology and Population Health (Z.W., B.A.P., T.W., X.X., Y.M.-R., C.R.I., R.D.B., R.C.K., Q.Q.), Albert Einstein College of Medicine, Bronx, NY.
Circ Res ; 134(7): 842-854, 2024 Mar 29.
Article in En | MEDLINE | ID: mdl-38547246
ABSTRACT

BACKGROUND:

Consistent evidence suggests diabetes-protective effects of dietary fiber intake. However, the underlying mechanisms, particularly the role of gut microbiota and host circulating metabolites, are not fully understood. We aimed to investigate gut microbiota and circulating metabolites associated with dietary fiber intake and their relationships with type 2 diabetes (T2D).

METHODS:

This study included up to 11 394 participants from the HCHS/SOL (Hispanic Community Health Study/Study of Latinos). Diet was assessed with two 24-hour dietary recalls at baseline. We examined associations of dietary fiber intake with gut microbiome measured by shotgun metagenomics (350 species/85 genera and 1958 enzymes; n=2992 at visit 2), serum metabolome measured by untargeted metabolomics (624 metabolites; n=6198 at baseline), and associations between fiber-related gut bacteria and metabolites (n=804 at visit 2). We examined prospective associations of serum microbial-associated metabolites (n=3579 at baseline) with incident T2D over 6 years.

RESULTS:

We identified multiple bacterial genera, species, and related enzymes associated with fiber intake. Several bacteria (eg, Butyrivibrio, Faecalibacterium) and enzymes involved in fiber degradation (eg, xylanase EC3.2.1.156) were positively associated with fiber intake, inversely associated with prevalent T2D, and favorably associated with T2D-related metabolic traits. We identified 159 metabolites associated with fiber intake, 47 of which were associated with incident T2D. We identified 18 of these 47 metabolites associated with the identified fiber-related bacteria, including several microbial metabolites (eg, indolepropionate and 3-phenylpropionate) inversely associated with the risk of T2D. Both Butyrivibrio and Faecalibacterium were associated with these favorable metabolites. The associations of fiber-related bacteria, especially Faecalibacterium and Butyrivibrio, with T2D were attenuated after further adjustment for these microbial metabolites.

CONCLUSIONS:

Among United States Hispanics/Latinos, dietary fiber intake was associated with favorable profiles of gut microbiota and circulating metabolites for T2D. These findings advance our understanding of the role of gut microbiota and microbial metabolites in the relationship between diet and T2D.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 / Gastrointestinal Microbiome Limits: Humans Language: En Journal: Circ Res Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 / Gastrointestinal Microbiome Limits: Humans Language: En Journal: Circ Res Year: 2024 Document type: Article