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The Genetic Challenges and Opportunities in Advanced Heart Failure

机译:晚期心力衰竭的遗传挑战和机遇

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The causes of heart failure are diverse. Inherited causes represent an important clinical entity and can be divided into 2 major categories: familial and metabolic cardiomyopathies. The distinct features that might be present in early disease states can become broadly overlapping with other diseases, such as in the case of inherited cardiomyopathies (ie, familial hypertrophic cardiomyopathy or mitochondrial diseases). In this review article, we focus on genetic issues related to advanced heart failure. Because of the emerging importance of this topic and its breadth, we sought to focus our discussion on the known genetic forms of heart failure syndromes, genetic testing, and newer data on pharmacogenetics and therapeutics in the treatment of heart failure, to primarily encourage clinicians to place a priority on the diagnosis and treatment of these potentially treatable conditions.
机译:心力衰竭的原因多种多样。遗传原因代表重要的临床实体,可以分为两大类:家族性和代谢性心肌病。在早期疾病状态中可能出现的独特特征可能与其他疾病广泛重叠,例如在遗传性心肌病(即家族性肥厚性心肌病或线粒体疾病)的情况下。在这篇评论文章中,我们关注与晚期心力衰竭有关的遗传问题。由于该主题的重要性及其广度,我们试图将讨论的重点放在心力衰竭综合征的已知遗传形式,基因测试以及用于心力衰竭的药物遗传学和疗法的最新数据上,以主要鼓励临床医生将这些潜在可治疗疾病的诊断和治疗放在优先位置。

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