Putko Brendan N, Yogasundaram Haran, Chow Kelvin, Pagano Joseph, Khan Aneal, Paterson D Ian, Thompson Richard B, Oudit Gavin Y
Division of Cardiology, Department of Medicine, Mazankowski Alberta Heart Institute, University of Alberta, 2C2 Walter Mackenzie Health Sciences Centre, Edmonton, Alberta, Canada.
Department of Biomedical Engineering, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Eur Heart J Cardiovasc Imaging. 2015 Oct;16(10):1129-36. doi: 10.1093/ehjci/jev057. Epub 2015 Mar 6.
Anderson-Fabry Disease (AFD) is an important cause of cardiomyopathy characterized by concentric left-ventricular hypertrophy (LVH). We evaluated the extent of left-atrial (LA) structural and functional remodelling in this group of patients given that LA remodelling is a marker of adverse outcomes in the presence of LVH.
Clinical profiles were obtained and cardiac MRI was performed in cohorts of patients with AFD (n = 31), healthy controls (n = 23), and a positive control cohort with known concentric remodelling and LVH (CR/H, n = 21). Of patients with AFD, 58% were on enzyme-replacement therapy (ERT), 84% were on renin-angiotensin system antagonism, and 65% were on statins. Despite a similar increase in LV mass index in the AFD when compared with the CR/H cohort, mean LA volumes for the AFD group were similar to those seen in the healthy control group. Following from this, we observed that the percentage contribution to LV stroke volume due to elastic/passive and active LA emptying was similar in the AFD and healthy control groups, while passive emptying was significantly lower in the CR/H group. The consequences of LVH in the AFD cohort were manifested in atrioventricular uncoupling, whereby the extent of elastic/passive and active LA emptying was not a function of the extent of longitudinal movement of the mitral annular plane, as it was in healthy control subjects.
Left-atrial structure and function were relatively normal in our cohort of patients with AFD, who were also judiciously treated with a contemporary strategy that includes renin-angiotensin system antagonism, statins, and ERT.
安德森-法布里病(AFD)是导致心肌病的重要原因,其特征为左心室向心性肥厚(LVH)。鉴于左心房(LA)重构是LVH存在时不良预后的标志物,我们评估了该组患者左心房结构和功能重构的程度。
获取了AFD患者队列(n = 31)、健康对照者队列(n = 23)以及已知存在向心性重构和LVH的阳性对照队列(CR/H,n = 21)的临床资料并进行了心脏磁共振成像检查。AFD患者中,58%接受酶替代疗法(ERT),84%接受肾素-血管紧张素系统拮抗剂治疗,65%接受他汀类药物治疗。尽管与CR/H队列相比,AFD患者的左心室质量指数有相似程度的增加,但AFD组的平均左心房容积与健康对照组相似。据此,我们观察到,AFD组和健康对照组中,弹性/被动及主动左心房排空对左心室每搏输出量的贡献百分比相似,而CR/H组的被动排空明显较低。AFD队列中LVH的后果表现为房室解耦,即弹性/被动及主动左心房排空的程度与二尖瓣环平面纵向运动的程度无关,而在健康对照者中是相关的。
在我们的AFD患者队列中,左心房结构和功能相对正常,这些患者也接受了包括肾素-血管紧张素系统拮抗剂、他汀类药物和ERT在内的现代策略的合理治疗。