Metabolic syndrome with and without C-reactive protein as a predictor of coronary heart disease and diabetes in the West of Scotland Coronary Prevention Study

被引:1106
作者
Sattar, N
Gaw, A
Scherbakova, O
Ford, I
O'Reilly, DS
Haffner, SM
Isles, C
Macfarlane, PW
Packard, CJ
Cobbe, SM
Shepherd, J
机构
[1] Glasgow Royal Infirm, Univ Dept Pathol Biochem, Glasgow G31 2ER, Lanark, Scotland
[2] Glasgow Royal Infirm, Clin Trials Unit, Glasgow G31 2ER, Lanark, Scotland
[3] Glasgow Royal Infirm, Div Cardiovasc & Med Sci, Glasgow G31 2ER, Lanark, Scotland
[4] Univ Glasgow, Robertson Ctr Biostat, Glasgow, Lanark, Scotland
[5] Univ Texas, Hlth Sci Ctr, Dept Med, San Antonio, TX 78284 USA
[6] Dept Med, Dumfries, Scotland
[7] Galloway Dist Gen Hosp, Dumfries, Scotland
关键词
insulin; coronary disease; obesity; inflammation; glucose;
D O I
10.1161/01.CIR.0000080897.52664.94
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-The National Cholesterol Education Program (NCEP) recently proposed a simple definition for metabolic syndrome. Information on the prospective association of this definition for coronary heart disease (CHD) and type 2 diabetes is currently limited. Methods and Results-We used a modified NCEP definition with body mass index in place of waist circumference. Baseline assessments in the West of Scotland Coronary Prevention Study were available for 6447 men to predict CHD risk and for 5974 men to predict incident diabetes over 4.9 years of follow-up. Mean LDL cholesterol was similar but C-reactive protein was higher (P<0.0001) in the 26% of men with the syndrome compared with those without. Metabolic syndrome increased the risk for a CHD event [univariate hazard ratio (HR) = 1.76 (95% CI, 1.44 to 2.15)] and for diabetes [univariate HR = 3.50 (95% CI 2.51 to 4.90)]. Metabolic syndrome continued to predict CHD events (HR = 1.30, 95% CI, 1.00 to 1.67, P = 0.045) in a multivariate model incorporating conventional risk factors. Men with 4 or 5 features of the syndrome had a 3.7-fold increase in risk for CHD and a 24.5-fold increase for diabetes compared with men with none (both P<0.0001). C-reactive protein enhanced prognostic information for both outcomes. With pravastatin, men with the syndrome had similar risk reduction for CHD as compared with those without (HR, 0.73 and 0.69; pravastatin versus placebo). Conclusions-A modified NCEP metabolic syndrome definition predicts CHD events, and, more strikingly, new-onset diabetes, and thus helps identify individuals who may receive particular benefit from lifestyle measures to prevent these diseases.
引用
收藏
页码:414 / 419
页数:6
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