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.
机构:
New York Med Coll, Div Cardiol, Westchester Med Ctr, 100 Woods Rd,Macy Pavil,Suite 11, Valhalla, NY 10595 USANew York Med Coll, Div Cardiol, Westchester Med Ctr, 100 Woods Rd,Macy Pavil,Suite 11, Valhalla, NY 10595 USA
Panza, Julio A.
Naidu, Srihari S.
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New York Med Coll, Div Cardiol, Westchester Med Ctr, 100 Woods Rd,Macy Pavil,Suite 11, Valhalla, NY 10595 USANew York Med Coll, Div Cardiol, Westchester Med Ctr, 100 Woods Rd,Macy Pavil,Suite 11, Valhalla, NY 10595 USA