Plasma Biomarker Profiles for Premature and Nonpremature Coronary Heart Disease in Women

被引:1
作者
Dugani, Sagar B. [1 ,2 ,3 ]
Moorthy, M. Vinayaga [1 ,4 ,5 ]
Demler, Olga, V [1 ,4 ,5 ]
Li, Chunying [1 ,4 ,5 ]
Ridker, Paul M. [4 ,5 ]
Glynn, Robert J. [1 ,4 ,5 ]
Mora, Samia [1 ,4 ,5 ]
机构
[1] Brigham & Womens Hosp, Ctr Lipid Metabol, Boston, MA USA
[2] Mayo Clin, Div Hosp Internal Med, 200 First St SW, Rochester, MN 55905 USA
[3] Mayo Clin, Robert D & Patricia E Kern Ctr Sci Hlth Care Deliv, Div Hlth Care Delivery Res, Rochester, MN 55905 USA
[4] Harvard Med Sch, Brigham & Womens Hosp, Div Prevent, Boston, MA USA
[5] Harvard Med Sch, Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA USA
基金
美国国家卫生研究院;
关键词
DENSITY-LIPOPROTEIN CHOLESTEROL; RESIDUAL VASCULAR RISK; CARDIOVASCULAR-DISEASE; MYOCARDIAL-INFARCTION; INSULIN-RESISTANCE; PRIMARY PREVENTION; LIPIDS; ROSUVASTATIN; ASSOCIATION; EVENTS;
D O I
10.1093/clinchem/hvae007
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Premature coronary heart disease (CHD) is a major cause of death in women. We aimed to characterize biomarker profiles of women who developed CHD before and after age 65 years. Methods: In the Women's Health Study (median follow-up 21.5 years), women were grouped by age and timing of incident CHD: baseline age <65 years with premature CHD by age 65 years (25 042 women; 447 events) and baseline age >= 65 years with nonpremature CHD (2982 women; 351 events). Associations of 44 baseline plasma biomarkers measured using standard assays and a nuclear magnetic resonance (NMR)-metabolomics assay were analyzed using Cox models adjusted for clinical risk factors. Results: Twelve biomarkers showed associations only with premature CHD and included lipoprotein(a), which was associated with premature CHD [adjusted hazard ratio (HR) per SD: 1.29 (95% CI 1.17-1.42)] but not with nonpremature CHD [1.09(0.98-1.22)](P-interaction = 0.02). NMR-measured lipoprotein insulin resistance was associated with the highest risk of premature CHD [1.92 (1.52-2.42)] but was not associated with nonpremature CHD (P-interaction <0.001). Eleven biomarkers showed stronger associations with premature vs nonpremature CHD, including apolipoprotein B. Nine NMR biomarkers showed no association with premature or nonpremature CHD, whereas 12 biomarkers showed similar significant associations with premature and nonpremature CHD, respectively, including low-density lipoprotein (LDL) cholesterol [1.30(1.20-1.45) and 1.22(1.10-1.35)] and C-reactive protein [1.34(1.19-1.50) and 1.25(1.08-1.44)]. Conclusions: In women, a profile of 12 biomarkers was selectively associated with premature CHD, driven by lipoprotein(a) and insulin-resistant atherogenic dyslipoproteinemia. This has implications for the development of biomarker panels to screen for premature CHD.
引用
收藏
页码:768 / 779
页数:12
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