4.7 Article Proceedings Paper

Butyrate-Producing Bacteria and Insulin Homeostasis: The Microbiome and Insulin Longitudinal Evaluation Study (MILES)

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DIABETES
卷 71, 期 11, 页码 2438-2446

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AMER DIABETES ASSOC
DOI: 10.2337/db22-0168

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资金

  1. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Disease [R01-DK109588, P30-DK063491]
  2. National Center for Advancing Translational Sciences [UL1TR001420, UL1TR001881]
  3. Eris M. Field Chair in Diabetes Research
  4. U.S. Department of Agriculture, Agricultural Research Service [58-3092-5-001]

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Gut microbiome studies have identified associations between specific butyrate-producing bacteria and insulin homeostasis. Some of these bacteria have beneficial effects on metabolism, while others may be detrimental. Therefore, targeted microbiome-directed therapeutic measures for preventing or treating diabetes should focus on specific butyrate-producing taxa.
Gut microbiome studies have documented depletion of butyrate-producing taxa in type 2 diabetes. We analyzed associations between butyrate-producing taxa and detailed measures of insulin homeostasis, whose dysfunction underlies diabetes in 224 non-Hispanic Whites and 129 African Americans, all of whom completed an oral glucose tolerance test. Stool microbiome was assessed by whole-metagenome shotgun sequencing with taxonomic profiling. We examined associations among 36 butyrate-producing taxa (n = 7 genera and 29 species) and insulin sensitivity, insulin secretion, disposition index, insulin clearance, and prevalence of dysglycemia (prediabetes plus diabetes, 46% of cohort), adjusting for age, sex, BMI, and race. The genus Coprococcus was associated with higher insulin sensitivity (beta = 0.14; P = 0.002) and disposition index ( beta = 0.12; P = 0.012) and a lower rate of dysglycemia (odds ratio [OR] 0.91; 95% CI 0.85-0.97; P = 0.0025). In contrast, Flavonifractor was associated with lower insulin sensitivity ( beta = -0.13; P = 0.004) and disposition index ( b = 20.11; P = 0.04) and higher prevalence of dysglycemia (OR 1.22; 95% CI 1.08-1.38; P = 0.0013). Species-level analyses found 10 bacteria associated with beneficial directions of effects and two bacteria with adverse associations on insulin homeostasis and dysglycemia. Although most butyrate producers analyzed appear to be metabolically beneficial, this is not the case for all such bacteria, suggesting that microbiome-directed therapeutic measures to prevent or treat diabetes should be targeted to specific butyrate producing taxa rather than all butyrate producers.

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