4.8 Article

Decreased Abundance of Akkermansia muciniphila Leads to the Impairment of Insulin Secretion and Glucose Homeostasis in Lean Type 2 Diabetes

期刊

ADVANCED SCIENCE
卷 8, 期 16, 页码 -

出版社

WILEY
DOI: 10.1002/advs.202100536

关键词

3 beta-chenodeoxycholic acid; Akkermansia muciniphila; bile acids; glucose tolerance; gut microbiota; insulin secretion; lean with type 2 diabetes

资金

  1. National Natural Science Foundation of China (NSFC) major international (regional) joint research project [81220108006]
  2. NSFC-NHMRC joint research grant [81561128016]
  3. Shanghai Municipal Key Clinical Specialty
  4. National Key Research and Development Program of China [2018YFA0800402]
  5. Marie Skodowska-Curie Actions (MSCA) and Innovative Training Networks [H2020-MSCA-ITN-2018 813781]
  6. DFG under Germany's Excellence Strategy [EXC 2051 (390713860)]
  7. General Program of NSFC [81870598]
  8. Excellent Young Scholars of NSFC [82022012]
  9. Two Hundred Program from Shanghai Jiao Tong University School of Medicine [20191830]

向作者/读者索取更多资源

The study found that the decreased abundance of A. muciniphila in lean individuals with T2D is associated with impaired insulin secretion and glucose homeostasis, and supplementation of A. muciniphila can protect mice from sucrose-induced damage.
Although obesity occurs in most of the patients with type 2 diabetes (T2D), a fraction of patients with T2D are underweight or have normal weight. Several studies have linked the gut microbiome to obesity and T2D, but the role of gut microbiota in lean individuals with T2D having unique clinical characteristics remains unclear. A metagenomic and targeted metabolomic analysis is conducted in 182 lean and abdominally obese individuals with and without newly diagnosed T2D. The abundance of Akkermansia muciniphila (A. muciniphila) significantly decreases in lean individuals with T2D than without T2D, but not in the comparison of obese individuals with and without T2D. Its abundance correlates inversely with serum 3 beta-chenodeoxycholic acid (beta CDCA) levels and positively with insulin secretion and fibroblast growth factor 15/19 (FGF15/19) concentrations. The supplementation with A. muciniphila is sufficient to protect mice against high sucrose-induced impairment of glucose intolerance by decreasing beta CDCA and increasing insulin secretion and FGF15/19. Furthermore, beta CDCA inhibits insulin secretion and FGF15/19 expression. These findings suggest that decreased abundance of A. muciniphila is linked to the impairment of insulin secretion and glucose homeostasis in lean T2D, paving the way for new therapeutic options for the prevention or treatment of diabetes.

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