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三级医疗中心队列中终末期肥厚型心肌病患者的临床特征与预后:收缩功能障碍和晚期舒张功能障碍

Clinical Characteristics and Prognosis of Patients with End-Stage Hypertrophic Cardiomyopathy from a Tertiary Center Cohort: Systolic Dysfunction and Advanced Diastolic Dysfunction.

作者信息

Afana Andreea Sorina, Adam Robert Daniel, Militaru Sebastian, Onciul Sebastian, Andrei Oana, Chirita Emandi Adela, Puiu Maria, Militaru Constantin, Jurcut Ruxandra

机构信息

Expert Center for Genetic Cardiovascular Diseases, Emergency Institute for Cardiovascular Diseases, 258 Fundeni Street, 022328 Bucharest, Romania.

Emergency Clinical County Hospital Craiova, 1 Tabaci Street, 200642 Craiova, Romania.

出版信息

Diagnostics (Basel). 2025 Apr 29;15(9):1134. doi: 10.3390/diagnostics15091134.

Abstract

: Hypertrophic cardiomyopathy (HCM) is a genetic disorder marked by myocardial hypertrophy, leading to diastolic and systolic dysfunction and heart failure. Traditionally, the burn-out stage is defined by systolic dysfunction, but we propose expanding its definition to include advanced diastolic dysfunction. : We retrospectively analyzed HCM patients (2004-2023) with either systolic dysfunction (left ventricular ejection fraction [LVEF] < 50%) or advanced diastolic dysfunction (preserved LVEF with left atrial enlargement and elevated filling pressures: E/A ≥ 2 or E/e' ≥ 14). Both subgroups were included under the term "end-stage HCM" and compared to HCM controls with preserved LVEF and impaired relaxation. : Of 696 HCM patients, 94 had end-stage HCM (23 with systolic dysfunction, 71 with advanced diastolic dysfunction). Median age was 56.5 years, and 55.3% were male. End-stage HCM patients were more symptomatic at follow-up than controls (91.5% vs. 75.0%, -value = 0.006), with higher rates of dyspnea and advanced heart failure (38.3% vs. 6.3%, -value < 0.001). Advanced diastolic dysfunction was associated with a more symptomatic profile (-value = 0.013) and a high annual mortality rate (2.34%, = 0.014). Male sex, older age, lower LVEF, and higher E/A predicted systolic dysfunction. : Advanced diastolic dysfunction represents an alternative progression pathway in burn-out HCM, requiring distinct management strategies alongside systolic dysfunction.

摘要

肥厚型心肌病(HCM)是一种以心肌肥厚为特征的遗传性疾病,可导致舒张功能和收缩功能障碍以及心力衰竭。传统上,疾病终末期是由收缩功能障碍定义的,但我们建议扩大其定义,将晚期舒张功能障碍也包括在内。

我们回顾性分析了2004年至2023年期间患有收缩功能障碍(左心室射血分数[LVEF]<50%)或晚期舒张功能障碍(LVEF正常但左心房增大且充盈压升高:E/A≥2或E/e'≥14)的HCM患者。这两个亚组都被纳入“终末期HCM”这一术语之下,并与LVEF正常但舒张功能受损的HCM对照组进行比较。

在696例HCM患者中,94例患有终末期HCM(23例有收缩功能障碍,71例有晚期舒张功能障碍)。中位年龄为56.5岁,55.3%为男性。终末期HCM患者在随访时比对照组症状更明显(91.5%对75.0%,P值=0.006),呼吸困难和晚期心力衰竭的发生率更高(38.3%对6.3%,P值<0.001)。晚期舒张功能障碍与症状更明显的情况相关(P值=0.013),且年死亡率较高(2.34%,P值=0.014)。男性、年龄较大、LVEF较低和E/A较高可预测收缩功能障碍。

晚期舒张功能障碍代表了疾病终末期HCM的另一种进展途径,除收缩功能障碍外还需要不同的管理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ae9/12071236/c0ef0585be34/diagnostics-15-01134-g001.jpg

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