Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Centre, Maastricht, the Netherlands; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands.
Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Centre, Maastricht, the Netherlands.
JACC Cardiovasc Imaging. 2020 Feb;13(2 Pt 2):549-558. doi: 10.1016/j.jcmg.2019.02.032. Epub 2019 Jun 12.
This study sought to investigate the prevalence of systolic dysfunction using global longitudinal strain (GLS) and its prognostic value in relatives of dilated cardiomyopathy (DCM) patients that had normal left ventricular ejection fraction (LVEF).
DCM relatives are advised to undergo cardiac assessment including echocardiography, irrespective of the genetic status of the index patient. Even though LVEF is normal, the question remains whether this indicates absence of disease or simply normal cardiac volumes. GLS may provide additional information regarding (sub)clinical cardiac abnormalities and thus allow earlier disease detection.
A total of 251 DCM relatives and 251 control subjects with a normal LVEF (≥55%) were screened. Automated software measured the GLS on echocardiographic 2-, 3-, and 4-chamber views. The cutoff value for abnormal strain was >-21.5. Median follow-up was 40 months (interquartile range: 5 to 80 months). Primary outcome was the combination of death and cardiac hospitalization.
A total of 120 relatives and 83 control subjects showed abnormal GLS (48% vs. 33%, respectively; p < 0.001). Abnormal GLS was independently associated with DCM relatives and cardiovascular risk factors, rather than genetic mutations. Subjects with abnormal GLS had more frequent cardiac hospitalizations and a higher mortality as compared with subjects with normal GLS (hazard ratio: 3.29; 95% confidence interval: 1.58 to 6.87; p = 0.001). Additionally, follow-up LVEF was measured in a subset of relatives, and it decreased significantly in those with abnormal as compared with normal GLS (p = 0.006).
Relatives of DCM patients had a significantly higher prevalence of systolic dysfunction detected by GLS despite normal LVEF compared with control subjects, independent of age, sex, comorbidities, and genotype. Abnormal GLS was associated with LVEF deterioration, cardiac hospitalization, and death.
本研究旨在探讨左心室射血分数(LVEF)正常的扩张型心肌病(DCM)患者亲属中,使用整体纵向应变(GLS)检测收缩功能障碍的患病率及其预后价值。
建议 DCM 亲属进行心脏评估,包括超声心动图检查,无论索引患者的遗传状态如何。即使 LVEF 正常,仍存在一个问题,即这是否表示不存在疾病,还是仅仅表示心脏容积正常。GLS 可能提供有关(亚)临床心脏异常的额外信息,从而能够更早地发现疾病。
共筛选了 251 名 DCM 亲属和 251 名 LVEF(≥55%)正常的对照者。自动软件在超声心动图 2 、 3 和 4 腔视图上测量 GLS。异常应变的截断值为>-21.5。中位随访时间为 40 个月(四分位距:5 至 80 个月)。主要结局是死亡和心脏住院的联合事件。
共有 120 名亲属和 83 名对照者的 GLS 异常(分别为 48%和 33%,p<0.001)。异常 GLS 与 DCM 亲属和心血管危险因素独立相关,而与基因突变无关。与 GLS 正常者相比,GLS 异常者更频繁地发生心脏住院和更高的死亡率(危险比:3.29;95%置信区间:1.58 至 6.87;p=0.001)。此外,在一部分亲属中测量了随访 LVEF,与 GLS 正常者相比,GLS 异常者的 LVEF 显著下降(p=0.006)。
尽管 LVEF 正常,但 DCM 患者亲属的 GLS 检测到收缩功能障碍的患病率明显高于对照组,独立于年龄、性别、合并症和基因型。异常 GLS 与 LVEF 恶化、心脏住院和死亡相关。