Insulin resistance in patients with cardiac hypertrophy

被引:108
作者
Paternostro, G
Pagano, D
Gnecchi-Ruscone, T
Bonser, RS
Camici, PG
机构
[1] Hammersmith Hosp, Imperial Coll, Sch Med, MRC,Cyclotron Unit, London W12 0NN, England
[2] Queen Elizabeth Hosp, Birmingham B15 2TH, W Midlands, England
基金
英国医学研究理事会;
关键词
glycolysis; heart failure; hypertrophy; membrane transport; valve (disease); positron emission tomography;
D O I
10.1016/S0008-6363(98)00233-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Animal studies suggest that left ventricular hypertrophy might be associated with insulin resistance and alterations in glucose transporters. We have previously demonstrated myocardial insulin resistance in patients with post-ischemic heart failure. The aim was to investigate whether myocardial insulin resistance could be demonstrated in human cardiac hypertrophy in the absence of hypertension, diabetes and coronary artery disease. Methods: Eleven normotensive nondiabetic patients with cardiac hypertrophy due to aortic stenosis and angiographically normal coronary arteries were compared to 11 normal volunteers. Myocardial glucose uptake (MGU) was measured with positron emission tomography and [F-18]2-fluoro-2-deoxy-D-glucose during fasting (low insulinemia) or during euglycemic-hyperinsulinemic clamp (physiologic hyperinsulinemia). Myocardial biopsies were obtained in order to investigate changes in insulin-independent (GLUT-1) and insulin-dependent (GLUT-LE) glucose transporters. Results: During fasting, plasma insulin (7+/-1 vs. 6+/-1 mU/l) and MGU (0.12+/-0.05 vs. 0.11+/-0.04 mu mol/min/g) were comparable in patients and controls. By contrast, during clamp, MGU was markedly reduced in patients (0.48+/-0.02 vs. 0.70+/-0.03 mu mol/min/g, p<0.01) despite similar plasma insulin levels (95+/-6 vs. 79+/-6 mU/l). A decreased GLUT-4/GLUT-1 ratio was shown by Western blot analysis in patients. Conclusions: Insulin resistance seems to be a feature of the hypertrophied heart even in the absence of hypertension, coronary artery disease and diabetes and may be explained, at least in part, by abnormalities in glucose transporters. (C) 1999 Published by Elsevier Science BN: All rights reserved.
引用
收藏
页码:246 / 253
页数:8
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