COPD的遗传易感性

A. Khan
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引用次数: 0

摘要

慢性阻塞性肺疾病(COPD)是全球发病率和死亡率的主要原因,以不可逆的气流阻塞为分类。根据世界卫生组织(世卫组织)的报告,慢性阻塞性肺病目前是第四大死因,到2030年,慢性阻塞性肺病将成为第三大死因。据观察,少数吸烟者有机会发展为慢性阻塞性肺病。但调查表明,吸烟后的其他因素似乎对慢性阻塞性肺病的发展起着重要作用。流行病学数据表明,遗传是其中一个因素,因为已知COPD在家族中聚集,这提供了遗传易感性在COPD中起重要作用的证据。COPD的相关性状和全基因组关联研究揭示了多个基因位点与COPD风险的关联。慢性阻塞性肺病的遗传性不能完全通过确定遗传危险因素来实现全基因组意义。遗传变异对COPD风险的相互影响尚未完全了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic predisposition to COPD
hronic obstructive pulmonary disease (COPD) is a major cause of global morbidity and mortality and categorized by irreversible airflow obstruction. COPD is presently the fourth leading cause of death and by 2030 COPD will be third leading cause of death according to the World Health Organization (WHO) reports. It was observe that minority of cigarette smokers have chance to develop COPD. But investigation suggests that subsequent to smoking other factors seems to be of play significant role for the development of the COPD. Epidemiological data demonstrated that genetics to be one of those factors, as COPD is known to aggregate in families and this provides evidence that genetic predisposition plays an important role in COPD. Related traits and genome wide association investigation of COPD have exposed multiple genetic loci association and risk of COPD. The heritability of COPD cannot be completely elucidated by identifying the genetic risk factors as achieving genome-wide significance. The mutual influence of genetic variation to COPD risk has not been completely understood.
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