Non-HDL cholesterol, apolipoproteins A-I and B100, standard lipid measures, lipid ratios, and CRP as risk factors for cardiovascular disease in women

被引:556
作者
Ridker, PM
Rifai, N
Cook, NR
Bradwin, G
Buring, JE
机构
[1] Brigham & Womens Hosp, Ctr Cardiovasc Dis Prevent, Boston, MA 02215 USA
[2] Brigham & Womens Hosp, Donald W Reynolds Ctr Cardiovasc Res, Boston, MA 02215 USA
[3] Brigham & Womens Hosp, Leducq Ctr Mol & Genet Epidemiol, Boston, MA 02215 USA
[4] Brigham & Womens Hosp, Div Prevent Med, Boston, MA 02215 USA
[5] Brigham & Womens Hosp, Div Cardiol, Boston, MA 02215 USA
[6] Harvard Univ, Childrens Hosp, Sch Med, Dept Lab Med, Boston, MA 02115 USA
[7] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2005年 / 294卷 / 03期
关键词
D O I
10.1001/jama.294.3.326
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Current guidelines for cardiovascular risk detection are controversial with regard to the clinical utility of different lipid measures, non-high-density lipoprotein cholesterol (non-HDL-C), lipid ratios, apolipoproteins, and C-reactive protein (CRP). Objective To directly compare the clinical utility of total cholesterol, low-density lipoprotein cholesterol (LDL-C), HDL-C, non HDL-C, apolipoproteins A-I and B-100, high-sensitivity CRP, and the ratios of total cholesterol to HDL-C, LDL-C to HDL-C, apolipoprotein B-100 to apolipoprotein A-I, and apolipoprotein B-100 to HDL-C as predictors of future cardiovascular events in women. Design, Setting, and Participants Prospective cohort study of 15 632 initially healthy US women aged 45 years or older (interquartile range, 48-59 years) who were enrolled between November 1992 and July 1995. All participants were followed up over a 10-year period for the occurrence of future cardiovascular events. Main Outcome Measure Hazard ratios (HRs) and 95% confidence intervals (Cls) for first-ever major cardiovascular events (N = 464) according to baseline levels of each biomarker. Results After adjustment for age, smoking status, blood pressure, diabetes, and body mass index, the HRs for future cardiovascular events for those in the extreme quintiles were 1.62 (95% Cl, 1.17-2.25) for LDL-C, 1.75 (95% Cl, 1.30-2.38) for apolipoprotein A-I, 2.08 (95% Cl, 1.45-2.97) for total cholesterol, 2.32 (95% Cl, 1.643.33) for HDL-C, 2.50 (95% Cl, 1.68-3.72) for apolipoprotein B-100, 2.51 (95% Cl, 1.69-3.72) for non-HDL-C, and 2.98 (95% Cl, 1.90-4.67) for high-sensitivity CRP (P<.001 for trend across all quintiles). The HRs for the lipid ratios were 3.01 (95% Cl, 2.01-4.50) for apolipoprotein B-100 to apolipoprotein A-I, 3.18 (95% Cl, 2.12-4.75) for LDL-C to HDL-C, 3.56 (95% Cl, 2.31-5.47) for apolipoprotein 13100 to HDL-C, and 3.81 (95% Cl, 2.47-5.86) for the total cholesterol to HDL-C (P<.001 for trend across all quintiles). The correlation coefficients between high-sensitivity CRP and the lipid parameters ranged from -0.33 to 0.15, and the clinical cut points for CRP of less than 1, 1 to 3, and higher than 3 mg/L provided prognostic information on risk across increasing levels of each lipid measure and lipid ratio. Conclusions Non-HDL-C and the ratio of total cholesterol to HDL-C were as good as or better than apolipoprotein fractions in the prediction of future cardiovascular events. After adjustment for age, blood pressure, smoking, diabetes, and obesity, high-sensitivity CRP added prognostic information beyond that conveyed by all lipid measures.
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页码:326 / 333
页数:8
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