From the Division of Preventive Medicine (S.M., A.O.A., C.M.A.) and Division of Cardiovascular Medicine (S.M., C.M.A.), Brigham and Women's Hospital, Harvard Medical School, Boston, MA; Division of Cardiology, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada (R.K.S.); and Department of Medicine, University Hospital, Basel, Switzerland (D.C.).
Circ Arrhythm Electrophysiol. 2014 Aug;7(4):612-9. doi: 10.1161/CIRCEP.113.001378. Epub 2014 May 25.
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.
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.
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.
ClinicalTrials.gov; Unique Identifier: NCT00000479.
低密度脂蛋白(LDL)胆固醇是动脉粥样硬化的一个强有力的危险因素,但与心房颤动(AF)呈负相关。我们旨在通过评估各种脂蛋白指标与房颤事件的关系,深入了解 LDL 胆固醇与房颤之间的这种矛盾关系。
我们前瞻性评估了 23738 名健康中年及以上女性(中位随访 16.4 年;N=795 例房颤事件)的脂蛋白指标。基线时直接测量 LDL 胆固醇,通过磁共振波谱法测量脂蛋白颗粒浓度和大小,并通过免疫测定法测量载脂蛋白。Cox 回归模型调整了年龄、房颤危险因素、炎症和糖代谢异常生物标志物。经过多变量调整后,观察到与房颤呈负相关(风险比,最高五分位与最低五分位的 95%置信区间,P 值):LDL 胆固醇(0.72,0.56-0.92,P=0.009)、LDL 颗粒总数(0.77,0.60-0.99,P=0.045)和极低密度脂蛋白颗粒(0.78,0.61-0.99,P=0.04),这主要是由于胆固醇含量低的小 LDL(0.78,0.61-1.00,P=0.05)和小极低密度脂蛋白颗粒(0.78,0.62-0.99,P=0.04)数量的减少。相比之下,较大的富含胆固醇的 LDL 颗粒和所有高密度脂蛋白指标在多变量模型中与房颤无关。对炎症和糖代谢异常生物标志物的调整对这些关联的影响很小。
在这项前瞻性研究中,LDL 胆固醇与房颤之间的负相关关系扩展到其他几种致动脉粥样硬化脂蛋白,这些关联不太可能是由直接的胆固醇作用介导的。
ClinicalTrials.gov;唯一标识符:NCT00000479。