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The Chromosome 9p21 Variant Not Predicting Long-Term Cardiovascular Mortality in Chinese with Established Coronary Artery Disease: An Eleven-Year Follow-Up Study

机译:染色体9p21变异不能预测中国已建立的冠状动脉疾病的长期心血管疾病死亡率:一项为期11年的随访研究

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摘要

Introduction. We examined whether the variant at chromosome 9p21, rs4977574, was associated with long-term cardiovascular mortality in Han Chinese patients with coronary artery disease (CAD). Methodology. Subjects who underwent coronary angiography for chest pain were consecutively enrolled. Fasting blood samples were collected for laboratory and genotype assessments. The information was correlated with data collected from the national death database. Results. There were 925 cases with CAD and 634 without CAD enrolled in the present study. The G allele conferred a significant increase in risk of CAD (odds ratio = 1.47, P = 0.003 in the dominant model; odds ratio = 1.36, P = 0.018 in the recessive model). During a median of 11 years (inter-quartile range between 5.2 and 12.5 years) of follow-up, neither the total nor the cardiovascular mortality was different among CAD subjects with different genotypes. Using Cox regression analysis, genotypes of rs4977574 still failed to predict cardiovascular mortality (hazard ratio = 1.25, P = 0.138 in the dominant model; hazard ratio = 1.05, P = 0.729 in the recessive model). Conclusions. The rs4977574 at chromosome 9p21 is associated with presence of CAD in Han Chinese. However, rs4977574 could not predict cardiovascular mortality in these CAD subjects during the eleven-year period of the study.
机译:介绍。我们检查了汉族冠心病(CAD)患者的9p21染色体变体rs4977574是否与长期心血管死亡相关。方法。连续入选因胸痛而接受冠状动脉造影的受试者。收集空腹血样用于实验室和基因型评估。该信息与从国家死亡数据库收集的数据相关。结果。本研究共入选925例CAD,634例无CAD。 G等位基因显着增加了CAD的风险(优势模型中优势比= 1.47,P = 0.003;隐性模型中优势比= 1.36,P = 0.018)。在中位随访11年(四分位之间介于5.2至12.5年之间),具有不同基因型的CAD受试者的总死亡率和心血管死亡率均无差异。使用Cox回归分析,rs4977574的基因型仍无法预测心血管疾病的死亡率(显性模型中的危险比= 1.25,P = 0.138;隐性模型中的危险比= 1.05,P = 0.729)。结论。 9p21染色体上的rs4977574与汉族人CAD的存在有关。但是,rs4977574无法在研究的十一年期间预测这些CAD受试者的心血管死亡率。

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