Effect of orlistat-assisted weight rose in decreasing coronary heart disease risk in patients with syndrome X

被引:55
作者
Reaven, G
Segal, K
Hauptman, J
Boldrin, M
Lucas, C
机构
[1] Roche Labs Inc, Nutley, NJ USA
[2] Stanford Univ, Sch Med, Stanford, CA 94305 USA
关键词
D O I
10.1016/S0002-9149(00)01521-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study describes the changes in risk factors for coronary heart disease in obese persons with syndrome X after orlistat-assisted weight loss. Data were available for 1,700 patients who completed 52 weeks of weight loss; 128 were defined as having syndrome X by being in the quintile with the highest plasma triglyceride levels (>2.2 mM/L) and the lowest high-density lipoprotein cholesterol (HDL, <1.0 mM/L) concentrations. Initial characteristics of those with syndrome X were similar to the 119 subjects (non-syndrome X) in the lowest quintile of plasma triglyceride (<0.975 mM/L) and highest quintile of HDL cholesterol (>1.5 mM/L). Subjects were placed on a calorie-restricted diet, and randomized to receive orlistat or placebo. Initial values were higher in those with syndrome X for diastolic blood pressure (p = 0.03), plasma insulin (p = 0.0001), triglyceride (p = 0.0001) concentrations, and ratio of low-density lipoprotein cholesterol to HDL cholesterol (p = 0.0001), and were lower for HDL cholesterol (p = 0.001) concentrations. Weight loss was greater in both groups of orlistat-treated patients (p = 0.026); in those with syndrome X, it was associated with a significant reduction in plasma insulin (p = 0.019) and triglyceride (p = 0.0001) concentrations, an increase in HDL cholesterol concentration, and a decrease in low-density lipoprotein/HDL cholesterol ratio (p = 0.0001), There were no significant changes in plasma insulin, triglycerides, or HDL cholesterol concentration in the non-syndrome X group. In conclusion, weight loss attenuates coronary heart disease risk factors in obese persons with syndrome X, and the risk factor reduction is enhanced with administration of orlistat. (C) 2001 by Excerpta Medico, Inc.
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收藏
页码:827 / 831
页数:5
相关论文
共 25 条
[1]   Comparison of plasminogen activator inhibitor-1 concentration in insulin-resistant versus insulin-sensitive healthy women [J].
Abbasi, F ;
McLaughlin, T ;
Lamendola, C ;
Lipinska, I ;
Tofler, G ;
Reaven, GM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (11) :2818-2821
[2]  
[Anonymous], 1987, FUNDAMENTALS CLIN CH
[3]   Hypertriglyceridemia and elevated lipoprotein(a) are risk factors for major coronary events in middle-aged men [J].
Assmann, G ;
Schulte, H ;
vonEckardstein, A .
AMERICAN JOURNAL OF CARDIOLOGY, 1996, 77 (14) :1179-1184
[4]  
AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
[5]   RELATIONSHIP BETWEEN DEGREE OF OBESITY AND INVIVO INSULIN ACTION IN MAN [J].
BOGARDUS, C ;
LILLIOJA, S ;
MOTT, DM ;
HOLLENBECK, C ;
REAVEN, G .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (03) :E286-E291
[6]  
CRIQUI NH, 1986, NEW ENGL J MED, V328, P1220
[7]  
Depres JP, 1996, NEW ENGL J MED, V334, P952
[8]   RELATIONSHIP BETWEEN RESISTANCE TO INSULIN-MEDIATED GLUCOSE-UPTAKE, URINARY URIC-ACID CLEARANCE, AND PLASMA URIC-ACID CONCENTRATION [J].
FACCHINI, F ;
CHEN, YDI ;
HOLLENBECK, CB ;
REAVEN, GM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 266 (21) :3008-3011
[9]   IMMUNOASSAY OF INSULIN WITH INSULIN-ANTIBODY PRECIPITATE [J].
HALES, CN ;
RANDLE, PJ .
BIOCHEMICAL JOURNAL, 1963, 88 (01) :137-&
[10]  
Hokanson J E, 1996, J Cardiovasc Risk, V3, P213, DOI 10.1097/00043798-199604000-00014