Gong Ling, Chen Jinxing, Lu Jinguo, Fan Lizi, Huang Jinghan, Zhang Yu, Lv Bin, Hui Rutai, Wang Yibo
State Key Laboratory of Cardiovascular Disease, Sino-German Laboratory for Molecular Medicine, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Radiology, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
PLoS One. 2014 Apr 14;9(4):e94823. doi: 10.1371/journal.pone.0094823. eCollection 2014.
Variants at the 9p21 locus have been associated with coronary artery disease (CAD); coronary artery calcification (CAC) is related to CAD and other cardiovascular events. To determine the association of the 9p21 locus with CAD in the presence and absence of CAC, 4 groups were enrolled in a case-control study, including 527 CAD patients without CAC, 692 CAD patients with CAC, 585 individuals with simple CAC but no CAD, and 725 healthy controls. The rs1333049 representing the locus was associated with CAD in the presence of CAC (odds ratio = 1.38 in allelic analysis, 95%CI, 1.19-1.60, P<0.001), but not in the absence of CAC. Additionally, rs1333049 was not associated with simple CAC or CAC severity/extent in CAD patients with CAC. 849 CAD patients undergoing revascularization (660 with CAC and 189 without CAC) were enrolled in a cohort study to test its association with cardiovascular events in CAD patients with and without CAC in a 3-year follow-up. rs1333049 was significantly associated with the incidence of cardiovascular events in non-target vessels in patients with CAC (hazard ratio = 1.44, 95%CI, 1.08-1.91, P = 0.012), but not in those without CAC. The variants at the 9p21 locus were related to CAD and post-revascularization events only in the presence of CAC, suggesting that they may confer risk of calcification-related coronary atherosclerosis.
9p21基因座的变异与冠状动脉疾病(CAD)相关;冠状动脉钙化(CAC)与CAD及其他心血管事件有关。为了确定在存在和不存在CAC的情况下9p21基因座与CAD的关联,4组人群被纳入一项病例对照研究,包括527例无CAC的CAD患者、692例有CAC的CAD患者、585例仅有CAC但无CAD的个体以及725例健康对照。代表该基因座的rs1333049在存在CAC的情况下与CAD相关(等位基因分析中优势比=1.38,95%可信区间,1.19 - 1.60,P<0.001),但在不存在CAC时则不然。此外,rs1333049与有CAC的CAD患者的单纯CAC或CAC严重程度/范围无关。849例接受血运重建的CAD患者(660例有CAC和189例无CAC)被纳入一项队列研究,以在3年随访中测试其与有和无CAC的CAD患者心血管事件的关联。rs1333049与有CAC患者非靶血管中心血管事件的发生率显著相关(风险比=1.44,95%可信区间,1.08 - 1.91,P = 0.012),但在无CAC患者中并非如此。9p21基因座的变异仅在存在CAC的情况下与CAD及血运重建后事件相关,这表明它们可能赋予钙化相关冠状动脉粥样硬化的风险。