医学
心肌病
心力衰竭
扩张型心肌病
心脏病学
内科学
猝死
心源性猝死
药物遗传学
心脏移植
肥厚性心肌病
遗传学
基因型
基因
生物
作者
Philippe Charron,Michel Galinier
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2002-05-01
卷期号:3 (3): 367-378
被引量:19
标识
DOI:10.1517/14622416.3.3.367
摘要
Cardiomyopathies are diseases of the myocardium associated with cardiac dysfunction, and are classified as dilated cardiomyopathy (DCM), hypertropic cardiomyopathy (HCM) and restrictive cardiomyopathy. Heart failure and sudden death are the two major complications. Also, since DCM is the primary indication for heart transplantation and HCM the primary cause of sudden death in young athletes, the socioeconomic impact of these diseases is important. Recently, the role of the genetic background in both monogenic and multifactorial cardiomyopathies has been studied, which has led to a better understanding of the underlying mechanisms that promote the development and progression of these diseases. Preliminary data suggest interactions between pharmacological treatment and genetic polymorphisms, which appear to be the first steps towards the application of phamacogenetics in heart failure.
科研通智能强力驱动
Strongly Powered by AbleSci AI