New perspectives in the pharmacological treatment of hypertrophic cardiomyopathy

被引:4
|
作者
Maltes, Sergio [1 ]
Lopes, Luis Rocha [2 ,3 ,4 ]
机构
[1] Univ Lisbon, Clin Univ Cardiol, Fac Med, Lisbon, Portugal
[2] UCL, Ctr Heart Muscle Dis, Inst Cardiovasc Sci, London, England
[3] St Bartholomews Hosp, Barts Heart Ctr, London, England
[4] Univ Lisbon, Fac Med, Ctr Cardiovasc, Lisbon, Portugal
基金
英国医学研究理事会;
关键词
Hylpertriaphic cardiomyopathy; Disease-modifying therapy; Pharmacotherapy; Genetic therapy; TRANSGENIC RABBIT MODEL; LEFT-VENTRICULAR HYPERTROPHY; CARDIAC-HYPERTROPHY; DILTIAZEM TREATMENT; EUROPEAN-SOCIETY; N-ACETYLCYSTEINE; WORKING GROUP; MOUSE MODEL; FIBROSIS; PERHEXILINE;
D O I
10.1016/j.repc.2019.03.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hypertrophic cardiomyopathy is an inherited cardiac disease and a major cause of heart failure and sudden death. Even though it was described more than 50 years ago, sarcomeric hypertrophic cardiomyopathy still lacks a disease-specific treatment. The drugs routinely used alleviate symptoms but do not prevent or revert the phenotype. With recent advances in the knowledge about the genetics and pathophysiology of hypertrophic cardiomyopathy, new genetic and pharmacological approaches have been recently discovered and studied that, by influencing different pathways involved in this disease, have the potential to function as disease modifying therapies. These promising new pharmacological and genetic therapies will be the focus of this review. (C) 2020 Sociedade Portuguesa de Cardiologia. Published by Elsevier Espana, S.L.U.
引用
收藏
页码:99 / 109
页数:11
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