Paradoxical Association of Lipoprotein Measures With Incident Atrial Fibrillation

被引:79
作者
Mora, Samia [1 ,2 ]
Akinkuolie, Akintunde O. [1 ]
Sandhu, Roopinder K. [3 ]
Conen, David [4 ]
Albert, Christine M. [1 ,2 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Prevent Med, Boston, MA 02115 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Cardiovasc Med, Boston, MA 02115 USA
[3] Univ Alberta, Dept Med, Div Cardiol, Edmonton, AB, Canada
[4] Univ Basel Hosp, Dept Med, CH-4031 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
apolipoproteins; atrial fibrillation; lipids; primary prevention; NUCLEAR-MAGNETIC-RESONANCE; NIIGATA PREVENTIVE MEDICINE; LIPID-LOWERING MEDICATIONS; METABOLIC SYNDROME; ATHEROSCLEROSIS RISK; CARDIOVASCULAR-DISEASE; APOLIPOPROTEIN-B; WOMEN; HEART; COMMUNITIES;
D O I
10.1161/CIRCEP.113.001378
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Low-density lipoprotein (LDL) cholesterol is a strong risk factor for atherosclerosis but has an inverse association with atrial fibrillation (AF). We aimed to provide insight into the paradoxical association of LDL cholesterol with AF by evaluating the relationship of various lipoprotein measures and incident AF. Methods and Results-We prospectively evaluated lipoprotein measures among 23 738 healthy middle-aged and older women (median follow-up 16.4 years; N=795 incident AF events). Baseline LDL cholesterol was directly measured, lipoprotein particle concentrations and size were measured by nuclear magnetic resonance spectroscopy, and apolipoproteins were measured by immunoassay. Cox regression models were adjusted for age, AF risk factors, inflammatory, and dysglycemic biomarkers. After multivariable adjustment, inverse associations with AF were observed (hazard ratio, 95% confidence interval for top versus bottom quintile, P value) for LDL cholesterol (0.72, 0.56-0.92, P=0.009), the total number of LDL particles (0.77, 0.60-0.99, P=0.045), and very-low-density lipoprotein particles (0.78, 0.61-0.99, P=0.04), which was driven by the number of cholesterol-poor small LDL (0.78, 0.61-1.00, P=0.05) and small very-low-density lipoprotein particles (0.78, 0.62-0.99, P=0.04). By contrast, the larger cholesterol-rich LDL particles and all high-density lipoprotein measures were not associated with AF in multivariable models. Adjustment for inflammatory and dysglycemic biomarkers had minimal impact on these associations. Conclusions-In this prospective study, the inverse association between LDL cholesterol and AF extended to several other atherogenic lipoproteins, and these associations are unlikely to be mediated by direct cholesterol effects.
引用
收藏
页码:612 / 619
页数:8
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