The biological variation of insulin resistance in polycystic ovarian syndrome

被引:26
作者
Jayagopal, V
Kilpatrick, ES
Holding, S
Jennings, PE
Atkin, SL
机构
[1] Univ Hull, Dept Med, Kingston Upon Hull HU3 2RW, N Humberside, England
[2] York Dist Gen Hosp, Kingston Upon Hull HU3 2RW, N Humberside, England
[3] Hull Royal Infirm, Dept Clin Biochem & Immunol, Kingston Upon Hull HU3 2RW, N Humberside, England
关键词
D O I
10.1210/jc.87.4.1560
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Increased insulin resistance (IR) is a cardinal feature of overweight patients with polycystic ovarian syndrome (PCOS). However, there are no data on the variability of IR for subjects with PCOS. The biological variation of IR (homeostasis model assessment model) was assessed by measuring IR at 4-d intervals on 10 consecutive occasions in 12 overweight PCOS patients (median age, 28 yr; range, 18-31 yr) and 11 weight-matched control women having regular menses and without PCOS (median age, 30 yr; range, 19-33 yr). The distribution of IR was log Gaussian in PCOS and Gaussian distribution in the control group. The IR in PCOS subjects was significantly greater than in the controls [mean (range), 5.85 U (1-42.1) vs. 1.67 U (0.48-3.49); P = 0.001]. After accounting for analytical variation, the mean intraindividual variance was also substantially greater in PCOS patients than in controls (mean, 1.19 vs. 0.23). As a consequence, at any level of IR, a subsequent sample must rise by more than 322% or fall by more than 31% to be considered significantly different from the first. IR, measured using the homeostasis model assessment model, is significantly greater and more variable for overweight patients with PCOS. Therefore, this inherent variability needs to be accounted for in studies of IR in PCOS.
引用
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页码:1560 / 1562
页数:3
相关论文
共 22 条
[1]   Ethnic differences in insulin resistance and its consequences in older Mexican American and non-hispanic white women [J].
Aguirre, MA ;
Jones, CNO ;
Pei, D ;
Villa, ML ;
Reaven, GM .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 1997, 52 (01) :M56-M60
[2]   INSULIN STIMULATES ANDROGEN ACCUMULATION IN INCUBATIONS OF OVARIAN STROMA OBTAINED FROM WOMEN WITH HYPERANDROGENISM [J].
BARBIERI, RL ;
MAKRIS, A ;
RANDALL, RW ;
DANIELS, G ;
KISTNER, RW ;
RYAN, KJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 62 (05) :904-910
[3]   Heterogeneity in beta cell activity, hepatic insulin clearance and peripheral insulin sensitivity in women with polycystic ovary syndrome [J].
Ciampelli, M ;
Fulghesu, AM ;
Cucinelli, F ;
Pavone, V ;
Caruso, A ;
Mancuso, S ;
Lanzone, A .
HUMAN REPRODUCTION, 1997, 12 (09) :1897-1901
[4]   beta-cell dysfunction independent of obesity and glucose intolerance in the polycystic ovary syndrome [J].
Dunaif, A ;
Finegood, DT .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (03) :942-947
[5]   Insulin resistance and the polycystic ovary syndrome: Mechanism and implications for pathogenesis [J].
Dunaif, A .
ENDOCRINE REVIEWS, 1997, 18 (06) :774-800
[6]   CHARACTERIZATION OF GROUPS OF HYPERANDROGENIC WOMEN WITH ACANTHOSIS NIGRICANS, IMPAIRED GLUCOSE-TOLERANCE, AND - OR HYPERINSULINEMIA [J].
DUNAIF, A ;
GRAF, M ;
MANDELI, J ;
LAUMAS, V ;
DOBRJANSKY, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1987, 65 (03) :499-507
[7]   Troglitazone improves defects in insulin action, insulin secretion, ovarian steroidogenesis, and fibrinolysis in women with polycystic ovary syndrome [J].
Ehrmann, DA ;
Schneider, DJ ;
Sobel, BE ;
Cavaghan, MK ;
Imperial, J ;
Rosenfield, RL ;
Polonsky, KS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (07) :2108-2116
[8]  
FERRANNINI E, 1991, DIABETOLOGIA, V34, P696
[9]   MEDICAL PROGRESS - POLYCYSTIC-OVARY-SYNDROME [J].
FRANKS, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (13) :853-861
[10]  
FRASER CG, 1989, CRIT REV CL LAB SCI, V27, P409