首页> 外文期刊>The Lancet >Inheritance of coronary artery disease in men: An analysis of the role of the y chromosome
【24h】

Inheritance of coronary artery disease in men: An analysis of the role of the y chromosome

机译:男性冠状动脉疾病的遗传:y染色体作用的分析

获取原文
获取原文并翻译 | 示例
           

摘要

Background: A sexual dimorphism exists in the incidence and prevalence of coronary artery disease - men are more commonly affected than are age-matched women. We explored the role of the Y chromosome in coronary artery disease in the context of this sexual inequity. Methods: We genotyped 11 markers of the male-specific region of the Y chromosome in 3233 biologically unrelated British men from three cohorts: the British Heart Foundation Family Heart Study (BHF-FHS), West of Scotland Coronary Prevention Study (WOSCOPS), and Cardiogenics Study. On the basis of this information, each Y chromosome was tracked back into one of 13 ancient lineages defined as haplogroups. We then examined associations between common Y chromosome haplogroups and the risk of coronary artery disease in cross-sectional BHF-FHS and prospective WOSCOPS. Finally, we undertook functional analysis of Y chromosome effects on monocyte and macrophage transcriptome in British men from the Cardiogenics Study. Findings: Of nine haplogroups identified, two (R1b1b2 and I) accounted for roughly 90 of the Y chromosome variants among British men. Carriers of haplogroup I had about a 50 higher age-adjusted risk of coronary artery disease than did men with other Y chromosome lineages in BHF-FHS (odds ratio 1·75, 95 CI 1·20-2·54, p=0·004), WOSCOPS (1·45, 1·08-1·95, p=0·012), and joint analysis of both populations (1·56, 1·24-1·97, p=0·0002). The association between haplogroup I and increased risk of coronary artery disease was independent of traditional cardiovascular and socioeconomic risk factors. Analysis of macrophage transcriptome in the Cardiogenics Study revealed that 19 molecular pathways showing strong differential expression between men with haplogroup I and other lineages of the Y chromosome were interconnected by common genes related to inflammation and immunity, and that some of them have a strong relevance to atherosclerosis. Interpretation: The human Y chromosome is associated with risk of coronary artery disease in men of European ancestry, possibly through interactions of immunity and inflammation. Funding: British Heart Foundation; UK National Institute for Health Research; LEW Carty Charitable Fund; National Health and Medical Research Council of Australia; European Union 6th Framework Programme; Wellcome Trust.
机译:背景:冠状动脉疾病的发病率和患病率存在​​性别差异-男性比同龄女性更容易受到影响。在这种性不平等的背景下,我们探讨了Y染色体在冠状动脉疾病中的作用。方法:我们对来自3个队列的3233个生物学上不相关的英国男性的11个Y染色体男性特定区域标记进行了基因分型:英国心脏基金会家庭心脏研究(BHF-FHS),苏格兰西部冠状动脉预防研究(WOSCOPS)和心源性研究。根据此信息,每个Y染色体都被追溯到被定义为单倍群的13个古老谱系之一。然后,我们在横断面BHF-FHS和前瞻性WOSCOPS中检查了常见的Y染色体单倍群与冠状动脉疾病风险的关联。最后,我们从《心脏成因研究》中对英国男性的Y染色体对单核细胞和巨噬细胞转录组的影响进行了功能分析。结果:在确定的九个单倍群中,两个(R1b1b2和I)构成了英国男性中Y染色体变异的大约90个。与BHF-FHS中具有其他Y染色体谱系的男性相比,单倍型I携带者的年龄调整后的冠状动脉疾病风险高50左右(优势比1·75、95 CI 1·20-2·54,p = 0· 004),WOSCOPS(1·45、1·08-1·95,p = 0·012)和两个种群的联合分析(1·56、1·24-1·97,p = 0·0002)。单倍群I与冠状动脉疾病风险增加之间的关联独立于传统的心血管和社会经济风险因素。在“心脏成因研究”中对巨噬细胞转录组的分析显示,有19条分子途径显示单倍基因组I的男性与Y染色体其他谱系之间的强烈差异表达与炎症和免疫相关的常见基因相互关联,其中一些与炎症和免疫相关。动脉粥样硬化。解释:在欧洲血统的男性中,人的Y染色体与冠状动脉疾病的风险相关,可能是由于免疫力和炎症的相互作用所致。资金来源:英国心脏基金会;英国国家卫生研究所; LEW Carty慈善基金;澳大利亚国家卫生和医学研究理事会;欧洲联盟第六框架计划;惠康信托。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号