van Velzen Hannah G, Schinkel Arend F L, Menting Myrthe E, van den Bosch Annemien E, Michels Michelle
Department of Cardiology, Thorax-center, Erasmus Medical Center, 's-Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands.
J Ultrasound. 2018 Sep;21(3):217-224. doi: 10.1007/s40477-018-0302-9. Epub 2018 Jun 6.
Previous studies suggest that anterior mitral valve leaflet (AMVL) elongation is a primary phenotypic feature in hypertrophic cardiomyopathy (HCM). Our aim was to assess AMVL length in individuals with HCM gene mutations and in healthy controls and to identify predictors of the development of HCM during follow-up.
A total of 133 HCM mutation carriers and 135 controls underwent cardiac examination including electro- and echocardiography. AMVL length was measured in the parasternal long axis and apical three chamber view during diastole. Univariate and multivariable cox proportional hazard regression analyses were performed to identify predictors of HCM.
There were no significant differences between HCM mutation carriers and controls regarding age and sex. In the parasternal long axis view, AMVL length was similar in mutation carriers and controls (24 ± 4 vs 24 ± 4 mm, p = 0.8). In the apical three chamber view, AMVL were shorter in mutation carriers (29 ± 4 vs 30 ± 4 mm, p = 0.02). When averaged for both views, AMVL length was similar in mutation carriers and controls (27 ± 3 vs 27 ± 3 mm, p = 0.2). During 5.8 ± 3.0 years follow-up, 13 (14%) HCM mutation carriers developed HCM. Pathological Q wave (hazard ratio 9.89, p = 0.004), E/e' ratio (hazard ratio 2.52, p = 0.001), and maximal wall thickness (hazard ratio 2.15, p = 0.001) were independent predictors of HCM. AMVL length was not predictive of the development of HCM.
AMVL length is similar in HCM mutation carriers and controls. AMVL length is not predictive of the development of HCM, in contrast to pathological Q wave, E/e' ratio, and maximal wall thickness.
先前的研究表明二尖瓣前叶(AMVL)延长是肥厚型心肌病(HCM)的主要表型特征。我们的目的是评估携带HCM基因突变的个体和健康对照者的AMVL长度,并确定随访期间HCM发生发展的预测因素。
总共133名HCM突变携带者和135名对照者接受了包括心电图和超声心动图在内的心脏检查。在舒张期于胸骨旁长轴和心尖三腔视图中测量AMVL长度。进行单变量和多变量Cox比例风险回归分析以确定HCM的预测因素。
HCM突变携带者和对照者在年龄和性别方面无显著差异。在胸骨旁长轴视图中,突变携带者和对照者的AMVL长度相似(24±4 vs 24±4mm,p = 0.8)。在心尖三腔视图中,突变携带者的AMVL较短(29±4 vs 30±4mm,p = 0.02)。当对两个视图进行平均时,突变携带者和对照者的AMVL长度相似(27±3 vs 27±3mm,p = 0.2)。在5.8±3.0年的随访期间,13名(14%)HCM突变携带者发生了HCM。病理性Q波(风险比9.89,p = 0.004)、E/e'比值(风险比2.52,p = 0.001)和最大壁厚(风险比2.15,p = 0.001)是HCM的独立预测因素。AMVL长度不能预测HCM的发生发展。
HCM突变携带者和对照者的AMVL长度相似。与病理性Q波、E/e'比值和最大壁厚不同,AMVL长度不能预测HCM的发生发展。