Triglyceride-rich very low-density lipoproteins (VLDL) are independently associated with insulin secretion in a multiethnic cohort of adolescents

Diabetes Obes Metab. 2018 Dec;20(12):2905-2910. doi: 10.1111/dom.13467. Epub 2018 Aug 2.

Abstract

Excess insulin secretion and hyperinsulinaemia contribute to the progression of type 2 diabetes. However, the mechanisms leading to insulin hypersecretion remain largely unknown. Based on our preliminary data, we examined whether triglycerides and very low-density lipoprotein (VLDL) are independently associated with insulin secretion, and whether ethnicity/race modulates these associations. Fasting triglycerides and VLDL were measured in a multiethnic cohort of 630 non-diabetic adolescents. Insulin secretion, β-cell function parameters, insulin sensitivity and insulin clearance were estimated through a 3-h oral glucose tolerance test. Metabolic assessments were repeated after 2 years in 239 subjects. Triglycerides and triglyceride-rich VLDL (large and medium size fractions) were associated with both basal and glucose-stimulated insulin secretion, after adjustment for age, sex, ethnicity, BMI z-score, plasma glucose, and insulin sensitivity. Ethnicity per se had an impact on lipid profile and β-cell function, but did not modulate the effect of triglycerides/VLDL on insulin secretion. At follow-up, changes in triglyceride levels were proportional to changes in insulin secretion. These findings support the hypothesis that hypertriglyceridaemia is an important stimulus for β-cell insulin release in young people under both fasting and fed conditions.

Keywords: beta cell function; clinical physiology; dyslipidaemia; glucose metabolism; insulin resistance, insulin secretion.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Blood Glucose / metabolism
  • Cohort Studies
  • Diabetes Mellitus, Type 2 / ethnology
  • Diabetes Mellitus, Type 2 / etiology
  • Fasting / blood
  • Female
  • Follow-Up Studies
  • Glucose Tolerance Test
  • Humans
  • Hyperinsulinism / ethnology
  • Hyperinsulinism / etiology
  • Hypertriglyceridemia / ethnology
  • Hypertriglyceridemia / etiology
  • Insulin Resistance / ethnology
  • Insulin Secretion / physiology*
  • Insulin-Secreting Cells / metabolism
  • Lipoproteins, VLDL / blood*
  • Male
  • Pediatric Obesity / blood*
  • Pediatric Obesity / complications
  • Pediatric Obesity / ethnology
  • Triglycerides / blood*

Substances

  • Blood Glucose
  • Lipoproteins, VLDL
  • Triglycerides
  • very low density lipoprotein triglyceride