From the Department of Medicine, Baylor College of Medicine and Methodist DeBakey Heart and Vascular Center, Houston, TX (R.C.H., J.W.G., W.S., J.J., S.S.V., C.M.B.); Human Genetics Center, University of Texas Health Science Center School of Public Health, Houston (R.C.D., J.R.C., E.B.); Department of Biostatistics, University of North Carolina at Chapel Hill (D.C.); Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX (S.S.V.); Center for Human Genetic Research and Cardiovascular Research Center, Massachusetts General Hospital, Boston (S.K.); and Department of Medicine, Harvard Medical School, Boston, MA (S.K.).
Arterioscler Thromb Vasc Biol. 2014 May;34(5):1069-77. doi: 10.1161/ATVBAHA.114.303284. Epub 2014 Feb 20.
OBJECTIVE: To investigate the relationship between plasma levels of small dense low-density lipoprotein-cholesterol (sdLDL-C) and risk for incident coronary heart disease (CHD) in a prospective study among Atherosclerosis Risk in Communities (ARIC) study participants. APPROACH AND RESULTS: Plasma sdLDL-C was measured in 11 419 men and women of the biracial ARIC study using a newly developed homogeneous assay. A proportional hazards model was used to examine the relationship among sdLDL-C, vascular risk factors, and risk for CHD events (n=1158) for a period of ≈11 years. Plasma sdLDL-C levels were strongly correlated with an atherogenic lipid profile and were higher in patients with diabetes mellitus than non-diabetes mellitus (49.6 versus 42.3 mg/dL; P<0.0001). In a model that included established risk factors, sdLDL-C was associated with incident CHD with a hazard ratio of 1.51 (95% confidence interval, 1.21-1.88) for the highest versus the lowest quartile, respectively. Even in individuals considered to be at low cardiovascular risk based on their LDL-C levels, sdLDL-C predicted risk for incident CHD (hazard ratio, 1.61; 95% confidence interval, 1.04-2.49). Genome-wide association analyses identified genetic variants in 8 loci associated with sdLDL-C levels. These loci were in or close to genes previously associated with risk for CHD. We discovered 1 novel locus, PCSK7, for which genetic variation was significantly associated with sdLDL-C and other lipid factors. CONCLUSIONS: sdLDL-C was associated with incident CHD in ARIC study participants. The novel association of genetic variants in PCSK7 with sdLDL-C and other lipid traits may provide new insights into the role of this gene in lipid metabolism.
目的:在动脉粥样硬化风险社区(ARIC)研究参与者的前瞻性研究中,研究血浆小而密低密度脂蛋白胆固醇(sdLDL-C)水平与冠心病(CHD)发病风险之间的关系。
方法和结果:采用新开发的均相测定法检测了 11419 名双种族 ARIC 研究中的男性和女性的血浆 sdLDL-C。使用比例风险模型,在约 11 年的时间内,检查 sdLDL-C、血管危险因素与 CHD 事件(n=1158)之间的关系。血浆 sdLDL-C 水平与致动脉粥样硬化脂质谱密切相关,且在糖尿病患者中高于非糖尿病患者(49.6 与 42.3mg/dL;P<0.0001)。在包含既定危险因素的模型中,sdLDL-C 与 CHD 发病相关,最高四分位与最低四分位相比,风险比为 1.51(95%置信区间,1.21-1.88)。即使在根据 LDL-C 水平被认为处于低心血管风险的个体中,sdLDL-C 也预测了 CHD 发病风险(风险比,1.61;95%置信区间,1.04-2.49)。全基因组关联分析确定了与 sdLDL-C 水平相关的 8 个基因座中的遗传变异。这些基因座位于或接近先前与 CHD 风险相关的基因。我们发现了一个新的基因座 PCSK7,其遗传变异与 sdLDL-C 和其他脂质因子显著相关。
结论:sdLDL-C 与 ARIC 研究参与者的 CHD 发病相关。PCSK7 中的遗传变异与 sdLDL-C 和其他脂质特征的新关联可能为该基因在脂质代谢中的作用提供新的见解。
Arterioscler Thromb Vasc Biol. 2014-2-20
Arterioscler Thromb Vasc Biol. 2013-11-14
J Atheroscler Thromb. 2020-7-1
Arterioscler Thromb Vasc Biol. 2013-6-13
Arterioscler Thromb Vasc Biol. 2025-8-14
BMC Cardiovasc Disord. 2025-6-3
Nutrients. 2025-4-11
Arterioscler Thromb Vasc Biol. 2013-11-14