Increased β-Cell Workload Modulates Proinsulin-to-Insulin Ratio in Humans

Diabetes. 2018 Nov;67(11):2389-2396. doi: 10.2337/db18-0279. Epub 2018 Aug 21.

Abstract

Increased proinsulin secretion, which characterizes type 2 diabetes and insulin resistance, may be due to an intrinsic, primitive defect in proinsulin processing or be secondary to increased demand on β-cells (hyperinsulinemia secondary to insulin resistance). An alternative way to investigate the relation between relative hyperproinsulinemia and increased secretory demand is to study the dynamic changes in the proinsulin-to-insulin ratio after partial pancreatectomy, a model of acute increased β-cell workload on the remaining pancreas. To pursue this aim, patients without diabetes, scheduled for partial pancreatectomy, underwent 4-h mixed-meal tests and hyperinsulinemic-euglycemic clamps before and after surgery. After acute β-cell mass reduction, no changes were observed in the fasting proinsulin-to-insulin ratio, whereas the fold change in the proinsulin-to-insulin ratio significantly increased over time after the meal. Further, our data demonstrate that whole-body insulin resistance is associated with underlying defects in proinsulin secretion, which become detectable only in the presence of increased insulin secretion demand.

Trial registration: ClinicalTrials.gov NCT02175459.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Glucose / metabolism*
  • Female
  • Glucose Clamp Technique
  • Humans
  • Insulin / blood*
  • Insulin-Secreting Cells / metabolism*
  • Lipids / blood*
  • Male
  • Middle Aged
  • Pancreatectomy
  • Proinsulin / blood*

Substances

  • Blood Glucose
  • Insulin
  • Lipids
  • Proinsulin

Associated data

  • ClinicalTrials.gov/NCT02175459