4.7 Article

Elevated Medium-Chain Acylcarnitines Are Associated With Gestational Diabetes Mellitus and Early Progression to Type 2 Diabetes and Induce Pancreatic beta-Cell Dysfunction

Journal

DIABETES
Volume 67, Issue 5, Pages 885-897

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/db17-1150

Keywords

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Funding

  1. Banting & Best Diabetes Center postdoctoral fellowship awards
  2. Canadian Institutes of Health Research doctoral research award
  3. Banting & Best Diabetes Center Scholarship
  4. Ontario Graduate Scholarship
  5. Canadian Institutes of Health Research operating grant [FDN-143219]
  6. Eunice Kennedy Shriver National Institute of Child Health and Human Development [R01-HD-050625, R01-HD-050625-03S1, R01-HD-050625-05S]
  7. National Institutes of Health National Center for Research Resources University of California, San Francisco-Clinical & Translational Science Institute [UL1-RR-024131]
  8. Kaiser Permanente Community Benefit Program (Northern California)
  9. Canadian Foundation for Innovation and Ontario Research Fund [30961]
  10. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT [R01HD050625] Funding Source: NIH RePORTER
  11. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK118409] Funding Source: NIH RePORTER

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Specific circulating metabolites have emerged as important risk factors for the development of diabetes. The acylcarnitines (acylCs) are a family of metabolites known to be elevated in type 2 diabetes (T2D) and linked to peripheral insulin resistance. However, the effect of acylCs on pancreatic beta-cell function is not well understood. Here, we profiled circulating acylCs in two diabetes cohorts: 1) women with gestational diabetes mellitus (GDM) and 2) women with recent GDM who later developed impaired glucose tolerance (IGT), new-onset T2D, or returned to normoglycemia within a 2-year follow-up period. We observed a specific elevation in serum medium-chain (M)-acylCs, particularly hexanoyl- and octanoylcarnitine, among women with GDM and individuals with T2D without alteration in long-chain acylCs. Mice treated with M-acylCs exhibited glucose intolerance, attributed to impaired insulin secretion. Murine and human islets exposed to elevated levels of M-acylCs developed defects in glucose-stimulated insulin secretion and this was directly linked to reduced mitochondrial respiratory capacity and subsequent ability to couple glucose metabolism to insulin secretion. In conclusion, our study reveals that an elevation in circulating M-acylCs is associated with GDM and early stages of T2D onset and that this elevation directly impairs beta-cell function.

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