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截断的肌联蛋白(TTN)变异与化疗诱导性心肌病。

Truncating Titin (TTN) Variants in Chemotherapy-Induced Cardiomyopathy.

机构信息

Department of Cardiology, Division of Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands.

Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

J Card Fail. 2017 Jun;23(6):476-479. doi: 10.1016/j.cardfail.2017.03.003. Epub 2017 Mar 14.

Abstract

Chemotherapy-induced cardiomyopathy (CCMP) is a complication of chemotherapy treatment occurring in 9% of patients treated with the use of anthracyclines. Currently, risk stratification is based on clinical risk factors that do not adequately account for variable individual susceptibility. This suggests the presence of other determinants. In this case series, we describe 2 women with breast cancer who developed severe heart failure within months after chemotherapy. Genetic screening revealed truncating frameshift mutations in TTN, encoding the myofilament titin, in both women. To our knowledge, this is the 1st report of an association between truncating TTN variants and CCMP. Because truncations in TTN are the most common cause of familial and sporadic dilated cardiomyopathy, further research is needed to establish their prevalence in patients presenting with CCMP.

摘要

化疗诱导性心肌病(CCMP)是化疗治疗的一种并发症,在使用蒽环类药物治疗的患者中,有 9%发生。目前,风险分层基于临床危险因素,但这些危险因素不能充分说明个体易感性的差异。这表明存在其他决定因素。在本病例系列中,我们描述了 2 例接受化疗后数月内发生严重心力衰竭的乳腺癌患者。基因筛查显示,这 2 名女性均存在编码肌丝titin 的 TTN 截断移码突变。据我们所知,这是首次报道截断 TTN 变异与 CCMP 之间存在关联。由于 TTN 中的截断是家族性和散发性扩张型心肌病的最常见原因,因此需要进一步研究来确定它们在出现 CCMP 的患者中的患病率。

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