Insulin secretory defect plays a major role in the development of diabetes in patients with distal pancreatectomy

Metabolism. 2006 Jan;55(1):135-41. doi: 10.1016/j.metabol.2005.08.005.

Abstract

To investigate the pathogenesis of distal pancreatectomy (d-Px)-induced diabetes in Korean patients, we investigated insulin secretory and sensitivity indexes obtained by oral glucose tolerance testing in 20 patients that had received d-Px (10 with d-Px-induced diabetes and 10 with normal glucose tolerance with d-Px [NGT d-Px]) and in 164 control subjects (77 with type 2 diabetes mellitus and 87 with NGT) that did not receive d-Px. The pancreatectomized subjects had lower fasting serum insulin, homeostasis model assessment of pancreatic beta-cell function (HOMA-beta) levels, and insulinogenic indices than the NGT controls. The HOMA-beta values of nonobese NGT d-Px- and d-Px-induced diabetic subjects were 73.7% and 38.7% of those for nonobese NGT controls, respectively, and HOMA-beta was significantly lower only for d-Px-induced diabetic subjects (P < .01). In obese subjects, the HOMA-beta values of obese d-Px-induced diabetic subjects were significantly lower than those of obese NGT controls (P < .05). The insulin sensitivity was significantly lower in nonobese type 2 diabetes mellitus controls than in nonobese NGT d-Px or in nonobese d-Px-induced diabetic subjects (P < .001 and .05, respectively). These results show that a reduced insulin secretory function is a typical feature of glucose homeostasis in distal pancreatectomized patients and that insulin secretory defect plays a major role in the development of diabetes in these patients. In addition, the study suggests that pancreatic resections of 60% or less and body mass index are not the main causes of diabetes onset after d-Px in this study.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blood Glucose / metabolism
  • Blood Pressure / physiology
  • Body Mass Index
  • C-Peptide / blood
  • Diabetes Mellitus / etiology*
  • Diabetes Mellitus / metabolism*
  • Diabetes Mellitus / physiopathology
  • Female
  • Humans
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin Resistance / physiology
  • Insulin Secretion
  • Lipids / blood
  • Male
  • Middle Aged
  • Pancreatectomy / adverse effects*

Substances

  • Blood Glucose
  • C-Peptide
  • Insulin
  • Lipids