NIDDM in the elderly

被引:66
作者
Meneilly, GS [1 ]
Elliott, T [1 ]
Tessier, D [1 ]
Hards, L [1 ]
Tildesley, H [1 ]
机构
[1] UNIV SHERBROOKE,DEPT MED,SHERBROOKE,PQ J1K 2R1,CANADA
关键词
D O I
10.2337/diacare.19.12.1320
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - We conducted this study to assess the metabolic alterations in elderly patients with NIDDM. RESEARCH DESIGN AND METHODS - Healthy lean (n = 15; age, 73 +/- 1 years; BMI, 23.8 +/- 0.5 kg/m(2)), and obese (n = 10; age, 71 +/- 1 years; BMI, 28.9 +/- 1.2 kg/m(2)) control subjects and lean (n = 10; age, 75 +/- 2 years; BMI, 24.0 +/- 0.5 kg/m(2)) and obese (n = 23; age, 73 +/- 1 years; BMI, 29.9 +/- 0.7 kg/m(2)) NIDDM patients underwent a 3-h glucose tolerance test, a 2-h hyperglycemic glucose clamp study and a 3-h euglycemic glucose clamp study with tritiated glucose methodology to measure glucose production and disposal rates. RESULTS - Waist-to-hip ratio (WHR) was greater in both lean and obese NIDDM patients than in control subjects. Insulin responses during the oral glucose tolerance test were similar in obese subjects (control subjects: 417 +/- 64 pmol/l; NIDDM patients: 392 +/- 47 pmol/l) but were reduced in lean NIDDM patients (control subjects: 374 +/- 34 pmol/l; NIDDM patients: 217 +/- 20 pmol/l, P < 0.01). Lean and obese NIDDM patients had absent first-phase insulin responses during the hyperglycemic clamp. Second-phase insulin responses were reduced in lean (P < 0.01 vs, control subjects by analysis of variance) but not obese NIDDM patients. Hepatic glucose output was not increased in lean or obese NIDDM patients. Steady-state (150-180 min) glucose disposal rates were 16% less in lean NIDDM patients (control subjects: 8.93 +/- 0.37 mg . kg LBM (lean body mass)(-1). min(-1); NIDDM patients: 7.50 +/- 0.28 mg . kg . LBM(-1). min(-1), P < 0.05) and 37% less in obese NIDDM patients (control subjects: 8.17 +/- 0.38 mg . kg . LBM(-1). min(-1); NIDDM patients: 5.03 +/- 0.36 mg . kg LBM(-1). min(-1), P < 0.001). CONCLUSIONS - Lean elderly NIDDM patients have a profound impairment in glucose-induced insulin release but mild resistance to insulin-mediated glucose disposal. Obese elderly NIDDM patients have adequate circulating insulin, but marked resistance to insulin-mediated glucose disposal Hepatic glucose output is not increased in elderly NIDDM patients.
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页码:1320 / 1325
页数:6
相关论文
共 29 条
[1]  
ANDRES R, 1966, AUTOMAT ANAL CHEM, P486
[2]   DIFFERENT ETIOLOGIES OF TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS IN OBESE AND NONOBESE SUBJECTS [J].
ARNER, P ;
POLLARE, T ;
LITHELL, H .
DIABETOLOGIA, 1991, 34 (07) :483-487
[3]   PATHOGENESIS OF TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES-MELLITUS - THE ROLE OF SKELETAL-MUSCLE GLUCOSE-UPTAKE AND HEPATIC GLUCOSE-PRODUCTION IN THE DEVELOPMENT OF HYPERGLYCEMIA - A CRITICAL COMMENT [J].
BECKNIELSEN, H ;
HOTHERNIELSEN, O ;
VAAG, A ;
ALFORD, F .
DIABETOLOGIA, 1994, 37 (02) :217-221
[4]   IMPACT OF OBESITY ON INSULIN ACTION IN NIDDM [J].
CAMPBELL, PJ ;
CARLSON, MG .
DIABETES, 1993, 42 (03) :405-410
[5]   PATHOGENESIS OF AGE-RELATED GLUCOSE-INTOLERANCE IN MAN - INSULIN RESISTANCE AND DECREASED BETA-CELL FUNCTION [J].
CHEN, M ;
BERGMAN, RN ;
PACINI, G ;
PORTE, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1985, 60 (01) :13-20
[6]   CONTRIBUTION OF OBESITY TO DEFECTS OF INTRACELLULAR GLUCOSE-METABOLISM IN NIDDM [J].
CHUNG, JW ;
SUH, KI ;
JOYCE, M ;
DITZLER, T ;
HENRY, RR .
DIABETES CARE, 1995, 18 (05) :666-673
[7]   PATHOGENESIS OF NIDDM - A BALANCED OVERVIEW [J].
DEFRONZO, RA ;
BONADONNA, RC ;
FERRANNINI, E .
DIABETES CARE, 1992, 15 (03) :318-368
[8]   MODELING ERROR AND APPARENT ISOTOPE DISCRIMINATION CONFOUND ESTIMATION OF ENDOGENOUS GLUCOSE-PRODUCTION DURING EUGLYCEMIC GLUCOSE CLAMPS [J].
FINEGOOD, DT ;
BERGMAN, RN ;
VRANIC, M .
DIABETES, 1988, 37 (08) :1025-1034
[9]  
FINK RI, 1983, J CLIN INVEST, V71, P1523, DOI 10.1172/JCI110908
[10]   INSULIN ACTION IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS - THE RELATIONSHIP BETWEEN HEPATIC AND EXTRAHEPATIC INSULIN RESISTANCE AND OBESITY [J].
FIRTH, R ;
BELL, P ;
RIZZA, R .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1987, 36 (11) :1091-1095