Hiruma Takashi, Inoue Shunsuke, Dai Zhehao, Nomura Seitaro, Kubo Toru, Sugiura Kenta, Suzuki Atsushi, Kashimura Takeshi, Matsushima Shouji, Yamada Takanobu, Tobita Takashige, Katoh Manami, Ko Toshiyuki, Ito Masamichi, Ishida Junichi, Amiya Eisuke, Hatano Masaru, Takeda Norifumi, Takimoto Eiki, Akazawa Hiroshi, Morita Hiroyuki, Yamaguchi Junichi, Inomata Takayuki, Tsutsui Hiroyuki, Kitaoka Hiroaki, Aburatani Hiroyuki, Takeda Norihiko, Komuro Issei
Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; Department of Frontier Cardiovascular Science, The University of Tokyo Graduate School of Medicine, Tokyo, Japan.
JACC Heart Fail. 2024 Dec;12(12):2041-2052. doi: 10.1016/j.jchf.2024.08.005. Epub 2024 Sep 25.
Approximately 10% of hypertrophic cardiomyopathy (HCM) patients have left ventricular systolic dysfunction (end-stage HCM) leading to severe heart-failure; however, risk stratification to identify patients at risk of progressing to end-stage HCM remains insufficient.
In this study, the authors sought to elucidate whether the coexistence of other cardiovascular disease (CVD)-related variants is associated with progression to end-stage HCM in patients with HCM harboring pathogenic or likely pathogenic (P/LP) sarcomeric variants.
The authors performed genetic analysis of 83 CVD-related genes in HCM patients from a Japanese multicenter cohort. P/LP variants in 8 major sarcomeric genes (MYBPC3, MYH7, TNNT2, TNNI3, TPM1, MYL2, MYL3, and ACTC1) definitive for HCM were defined as "sarcomeric variants." In addition, P/LP variants associated with other CVDs, such as dilated cardiomyopathy and arrhythmogenic cardiomyopathy, were referred to as "other CVD-related variants."
Among 394 HCM patients, 139 carried P/LP sarcomeric variants: 11 (7.9%) carried other CVD-related variants, 6 (4.3%) multiple sarcomeric variants, and 122 (87.8%) single sarcomeric variants. In a multivariable Cox regression analysis, presence of multiple sarcomeric variants (adjusted HR [aHR]: 3.35 [95% CI: 1.25-8.95]; P = 0.016) and coexistence of other CVD-related variants (aHR: 2.80 [95% CI: 1.16-6.78]; P = 0.022) were independently associated with progression to end-stage HCM. Coexisting other CVD-related variants were also associated with heart failure events (aHR: 2.75 [95% CI: 1.27-5.94]; P = 0.010).
Approximately 8% of sarcomeric HCM patients carried other CVD-related variants, which were associated with progression to end-stage HCM and heart failure events. Comprehensive surveillance of CVD-related variants within sarcomeric HCM patients contributes to risk stratification and understanding of mechanisms underlying end-stage HCM.
约10%的肥厚型心肌病(HCM)患者存在左心室收缩功能障碍(终末期HCM),导致严重心力衰竭;然而,用于识别有进展为终末期HCM风险患者的风险分层仍然不足。
在本研究中,作者试图阐明其他心血管疾病(CVD)相关变异的共存是否与携带致病性或可能致病性(P/LP)肌节变异的HCM患者进展为终末期HCM有关。
作者对来自日本多中心队列的HCM患者的83个CVD相关基因进行了基因分析。8个对HCM具有决定性意义的主要肌节基因(MYBPC3、MYH7、TNNT2、TNNI3、TPM1、MYL2、MYL3和ACTC1)中的P/LP变异被定义为“肌节变异”。此外,与其他CVD(如扩张型心肌病和致心律失常性心肌病)相关的P/LP变异被称为“其他CVD相关变异”。
在394例HCM患者中,139例携带P/LP肌节变异:11例(7.9%)携带其他CVD相关变异,6例(4.3%)携带多个肌节变异,122例(87.8%)携带单个肌节变异。在多变量Cox回归分析中,多个肌节变异的存在(调整后风险比[aHR]:3.35[95%置信区间:1.25 - 8.95];P = 0.016)和其他CVD相关变异的共存(aHR:2.80[95%置信区间:1.16 - 6.78];P = 0.022)与进展为终末期HCM独立相关。共存的其他CVD相关变异也与心力衰竭事件相关(aHR:2.75[95%置信区间:1.27 - 5.94];P = 0.010)。
约8%的肌节性HCM患者携带其他CVD相关变异,这与进展为终末期HCM和心力衰竭事件相关。对肌节性HCM患者进行CVD相关变异的综合监测有助于风险分层和理解终末期HCM的潜在机制。