4.7 Article

Progressive Shifts in the Gut Microbiome Reflect Prediabetes and Diabetes Development in a Treatment-Naive Mexican Cohort

Journal

FRONTIERS IN ENDOCRINOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2020.602326

Keywords

type 2 diabetes; microbiome; Mexico; metformin; deep phenotyping

Funding

  1. CONACYT (Grant Ciencia de Frontera 2019) [FORDECYT-PRONACES/425859/2020]
  2. National Institute of Genomic Medicine (INMEGEN, Mexico)
  3. University of Guanajuato [010/2014, 018/2015, 1098/2016]
  4. MIT International Science and Technology Initiatives (MISTI-2015-2016)
  5. CONACYT

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The study reveals a direct link between gut microbiome and Type 2 diabetes (T2D), with specific bacterial genera being closely associated with T2D prevalence and risk. Treatment, particularly using metformin, can restore the microbiome to a normoglycemic state and affect the progression of T2D.
Type 2 diabetes (T2D) is a global epidemic that affects more than 8% of the world's population and is a leading cause of death in Mexico. Diet and lifestyle are known to contribute to the onset of T2D. However, the role of the gut microbiome in T2D progression remains uncertain. Associations between microbiome composition and diabetes are confounded by medication use, diet, and obesity. Here we present data on a treatment-naive cohort of 405 Mexican individuals across varying stages of T2D severity. Associations between gut bacteria and more than 200 clinical variables revealed a defined set of bacterial genera that were consistent biomarkers of T2D prevalence and risk. Specifically, gradual increases in blood glucose levels, beta cell dysfunction, and the accumulation of measured T2D risk factors were correlated with the relative abundances of four bacterial genera. In a cohort of 25 individuals, T2D treatment-predominantly metformin-reliably returned the microbiome to the normoglycemic community state. Deep clinical characterization allowed us to broadly control for confounding variables, indicating that these microbiome patterns were independent of common T2D comorbidities, like obesity or cardiovascular disease. Our work provides the first solid evidence for a direct link between the gut microbiome and T2D in a critically high-risk population. In particular, we show that increased T2D risk is reflected in gradual changes in the gut microbiome. Whether or not these T2D-associated changes in the gut contribute to the etiology of T2D or its comorbidities remains to be seen.

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