The effect of orlistat-induced weight loss, without concomitant hypocaloric diet, on cardiovascular risk factors and insulin sensitivity in young obese chinese subjects with or without type 2 diabetes

被引:53
作者
Tong, PCY [1 ]
Lee, ZSK [1 ]
Sea, MM [1 ]
Chow, CC [1 ]
Ko, GTC [1 ]
Chan, WB [1 ]
So, WY [1 ]
Ma, RCW [1 ]
Ozaki, R [1 ]
Woo, J [1 ]
Cockram, CS [1 ]
Chan, JCN [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Med & Therapeut, Prince Wales Hosp, Shatin, Hong Kong, Peoples R China
关键词
D O I
10.1001/archinte.162.21.2428
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: We examined the weight-losing effect of orlistat treatment on insulin sensitivity and cardiovascular risk factors in a group of severely obese young Chinese patients with or without type 2 diabetes mellitus. Methods: Obese patients with diabetes (n = 33) and obese nondiabetic patients (n = 27) were given orlistat, 120 mg 3 times daily, without a concomitant hypocaloric diet for 6 months (body mass index [calculated as weight in kilograms divided by the square of height in meter; kg/m(2)] range, 27.8-47.4). The efficacy measures were (1) insulin sensitivity indices derived from the homeostasis model assessment and a composite measure of whole-body insulin sensitivity index; (2) glycemic control; (3) cardiovascular risk factors, including anthropometry, blood pressure, lipid profiles, and albuminuria; and (4) body composition determined by dual-energy x-ray absorptiometry. Results: At baseline, patients with diabetes had lower body mass index and percentage of body fat but higher waist-hip ratios and were more insulin resistant. Orlistat therapy reduced body weight, waist and hip circumferences, percentage of total body fat, blood pressure, fasting plasma glucose and lipid levels, albuminuria, and insulin sensitivity indices in both groups (all, P<.05). Despite less weight reduction, we found a greater percentage of reduction from baseline in glycosylated hemoglobin level (-11.6% vs -3.6%; P<.001), fasting plasma glucose level (-18.2% vs -5.0%; P<.001), and systolic blood pressure (-7.1% vs; -3.1%; P=.02) in patients with diabetes. Obese subjects without diabetes had greater improvements in triglyceride levels, albuminuria, and the homeostasis model assessment (all, P<.01). Conclusion: Short-term orlistat treatment without the use of a hypocaloric diet significantly improved insulin sensitivity and cardiovascular risk profiles in severely obese Chinese patients with or without type 2 diabetes.
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收藏
页码:2428 / 2435
页数:8
相关论文
共 53 条
[1]   Insulin resistance and obesity - The role of fat distribution pattern [J].
Abate, N .
DIABETES CARE, 1996, 19 (03) :292-294
[2]   Adipose tissue as an endocrine organ [J].
Ahima, RS ;
Flier, JS .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2000, 11 (08) :327-332
[3]   ASSESSMENT OF INSULIN ACTION AND GLUCOSE EFFECTIVENESS IN DIABETIC AND NONDIABETIC HUMANS [J].
ALZAID, AA ;
DINNEEN, SF ;
TURK, DJ ;
CAUMO, A ;
COBELLI, C ;
RIZZA, RA .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2341-2348
[4]   Visceral fat and cardiovascular risk factors in Chinese NIDDM patients [J].
Anderson, PJ ;
Chan, JCN ;
Chan, YL ;
Tomlinson, B ;
Young, RP ;
Lee, ZSK ;
Lee, KKC ;
Metreweli, C ;
Cockram, CS ;
Critchley, JAJH .
DIABETES CARE, 1997, 20 (12) :1854-1858
[5]  
[Anonymous], 2000, ASIA PACIFIC PERSPEC
[6]  
[Anonymous], 1995, Br. Med. J, DOI DOI 10.1136/BMJ.310.6972.83
[7]   Role of fatty acids in the pathogenesis of insulin resistance and NIDDM [J].
Boden, G .
DIABETES, 1997, 46 (01) :3-10
[8]   The metabolic syndrome in Hong Kong Chinese - The interrelationships among its components analyzed by structural equation modeling [J].
Chan, JCN ;
Cheung, JCK ;
Lau, EMC ;
Wooa, J ;
Chan, AYW ;
Swaminathan, R ;
Cockrama, CS .
DIABETES CARE, 1996, 19 (09) :953-959
[9]   Weight control and risk factor reduction in obese subjects treated for 2 years with orlistat - A randomized controlled trial [J].
Davidson, MH ;
Hauptman, J ;
DiGirolamo, M ;
Foreyt, JP ;
Halsted, CH ;
Heber, D ;
Heimburger, DC ;
Lucas, CP ;
Robbins, DC ;
Chung, J ;
Heymsfield, SB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (03) :235-242
[10]   INSULIN RESISTANCE - A MULTIFACETED SYNDROME RESPONSIBLE FOR NIDDM, OBESITY, HYPERTENSION, DYSLIPIDEMIA, AND ATHEROSCLEROTIC CARDIOVASCULAR-DISEASE [J].
DEFRONZO, RA ;
FERRANNINI, E .
DIABETES CARE, 1991, 14 (03) :173-194