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Peripheral and hepatic insulin sensitivity in subjects with impaired glucose tolerance
Authors:T S Berrish  C S Hetherington  K G M M Alberti  Dr M Walker
Institution:(1) Human Diabetes and Metabolism Research Centre, University of Newcastle upon Tyne, Newcastle upon Tyne, UK;(2) Department of Medicine, University of Newcastle upon Tyne, Newcastle upon Tyne, UK;(3) Biomedical Mass Spectrometry Unit, University of Newcastle upon Tyne, Newcastle upon Tyne, UK;(4) Department of Medicine, The Medical School, Framlington Place, NE2 4HH Newcastle upon Tyne, UK
Abstract:Summary Recent evidence suggests that the post-prandial hyperglycaemia in impaired glucose tolerance is primarily due to impaired suppression of basal hepatic glucose output. This in turn appears to be secondary to decreased first phase insulin secretion, although decreased hepatic insulin sensitivity, which is a feature of non-insulin-dependent diabetes mellitus, might also play a role. Eight mildly overweight subjects with impaired glucose tolerance and eight closely matched control subjects with normal glucose tolerance underwent an intravenous glucose tolerance test to assess first phase insulin secretion. Insulin sensitivity was examined by a 150-min hyperinsulinaemic-euglycaemic clamp. Somatostatin was infused from 150 min to suppress endogenous insulin secretion, and glucagon and insulin were replaced by constant infusion. Glucose with added dideuterated glucose (labelled infusion technique) was infused to maintain euglycaemia. First phase insulin secretion (Delta 0–10 min insulin area ÷Delta 0–10 min glucose area) was significantly decreased in the subjects with impaired glucose tolerance (median range]: 1.2 0.2–19.4] vs 9.1 2.6–14.5] mU·mmol–1; p<0.01). During the clamp, circulating insulin (93±8 mean±SEM] and 81±10 mU·l–1) and glucagon (54±4 and 44±6 ng·l–1) levels were comparable. Total glucose disposal was decreased in subjects with impaired glucose tolerance (2.78±0.27 vs 4.47±0.53 mg·kg–1·min–1; p<0.02), and was primarily due to decreased non-oxidative glucose disposal. However, hepatic glucose output rates were comparable during the clamp (0.38±0.10 and 0.30±0.18 mg·kg–1·min–1). Therefore, the main defects in subjects with impaired glucose tolerance are decreased first phase insulin secretion and peripheral non-oxidative glucose disposal, but hepatic glucose output shows normal responsiveness to insulin.Abbreviations FPIS First phase insulin secretion - PG plasma glucose - NIDDM non-insulin-dependent diabetes mellitus - IGT impaired glucose tolerance - HGO hepatic glucose output - IVGTT intravenous glucose tolerance test - OGTT oral glucose tolerance test
Keywords:Impaired glucose tolerance  insulin sensitivity  hepatic glucose output  insulin secretion  labelled infusion technique
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