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慢性阻塞性肺疾病的遗传学

Genetics of COPD.

作者信息

Molfino Néstor A

机构信息

Otsuka Maryland Research Institute, Rockville, MD 20850, USA.

出版信息

Chest. 2004 May;125(5):1929-40. doi: 10.1378/chest.125.5.1929.

Abstract

COPD is a complex mix of signs and symptoms in patients with chronic bronchitis and emphysema, diseases that largely result from cigarette smoking. Not all smokers, however, acquire COPD, and COPD can develop in nonsmokers. In the United States, COPD is currently the fourth leading cause of death. Surprisingly, there are no effective drug therapies for COPD that are able to significantly alter disease progression, and little is known of the underlying molecular mechanisms that are responsible for its occurrence. Candidate gene-association studies and linkage analyses have been reported for COPD patients. This review describes the genetic predisposition of healthy subjects or relatives of COPD patients to acquire COPD. In addition, the genetic bases of COPD with rapid decline of FEV1 are described, and the current genetic data that have been distilled from studies of COPD patients with a predominant emphysema phenotype, with chronic bronchitis phenotype, and with a response to bronchodilators are discussed.

摘要

慢性阻塞性肺疾病(COPD)是慢性支气管炎和肺气肿患者出现的一系列复杂的症状体征,而这两种疾病很大程度上是由吸烟导致的。然而,并非所有吸烟者都会患上COPD,不吸烟者也可能患COPD。在美国,COPD目前是第四大死因。令人惊讶的是,目前尚无能够显著改变疾病进展的有效药物疗法,对于其发病的潜在分子机制也知之甚少。已有针对COPD患者的候选基因关联研究和连锁分析的报道。本综述描述了健康受试者或COPD患者亲属患COPD的遗传易感性。此外,还描述了第一秒用力呼气容积(FEV1)快速下降的COPD的遗传基础,并讨论了从以肺气肿为主型、慢性支气管炎型以及对支气管扩张剂有反应的COPD患者研究中提炼出的当前遗传数据。

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