4.7 Article

A history of previous gestational diabetes mellitus is associated with adverse changes in insulin secretion and VLDL metabolism independently of increased intrahepatocellular lipid

Journal

DIABETOLOGIA
Volume 56, Issue 9, Pages 2021-2033

Publisher

SPRINGER
DOI: 10.1007/s00125-013-2956-3

Keywords

Acute insulin response to glucose; Adiposity; Disposition index; Gestational diabetes; Insulin resistance; Non-alcoholic fatty liver disease; Type 2 diabetes; VLDL metabolism

Funding

  1. Diabetes UK Clinical Intermediate Fellowship [BDA:RD04/0002483]
  2. Heart Disease and Diabetes Research Trust
  3. Medical Research Council
  4. British Heart Foundation Centre of Research Excellence, Edinburgh
  5. NHS Lothian Research and Development
  6. Wellcome Trust Clinical Research Facility, Edinburgh [E06372]
  7. Metabolic Unit, Imperial College, London
  8. Brain Research Imaging Centre
  9. SINAPSE (Scottish Imaging Network - A Platform for Scientific Excellence)
  10. Scottish Funding Council
  11. Chief Scientist Office
  12. Society for Endocrinology (S. Lethby, Imperial College, London)
  13. MRC [MC_U120061305] Funding Source: UKRI
  14. British Heart Foundation [RG/11/4/28734] Funding Source: researchfish
  15. Medical Research Council [MC_U120061305] Funding Source: researchfish

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We have previously reported a high prevalence of non-alcoholic fatty liver disease (NAFLD) among women with previous gestational diabetes mellitus (pGDM). We wanted to confirm that intrahepatocellular lipid (IHCL) is associated with pGDM independently of adiposity and determine: (1) if VLDL metabolism is dysregulated; and (2) the extent to which NAFLD and IHCL account for the dysmetabolic phenotype in pGDM. We analysed data from a cohort of 234 women (114 with pGDM) and identified effects of pGDM on lipid and glucoregulation that were independent of ultrasound-diagnosed NAFLD. We then measured IHCL by MR spectroscopy in a representative subgroup (n = 36) and conducted detailed metabolic studies (IVGTT, VLDL apolipoprotein B [apoB] kinetics and palmitate turnover) and measurement of regional body fat by MRI to demonstrate effects of IHCL that were independent of a history of pGDM. pGDM was associated with increased IHCL (p = 0.04) after adjustment for adiposity. Independently of IHCL, pGDM was associated with a lower IVGTT disposition index (p = 0.02) and acute insulin response to glucose (pGDM+/NAFLD-, 50% lower; pGDM+/NAFLD+, 36% lower; effect of pGDM, p = 0.03), increased VLDL apoB pool size (pGDM+/NAFLD-, 3.1-fold higher; pGDM+/NAFLD+, 1.2-fold higher; effect of pGDM, p = 0.02) and, at borderline significance (p = 0.05), increased rate of VLDL apoB synthesis. pGDM is associated with increased IHCL independently of adiposity. The increased liver fat contributes to the phenotype, but pGDM status is independently associated with diminished insulin secretion and (shown for the first time) augmented VLDL metabolism. IHCL with pGDM may compound a dysmetabolic phenotype.

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