Cardiovascular magnetic resonance demonstration of the spectrum of morphological phenotypes and patterns of myocardial scarring in Anderson-Fabry disease

被引:99
作者
Deva, Djeven Parameshvara [1 ]
Hanneman, Kate [2 ]
Li, Qin [3 ]
Ng, Ming Yen [2 ,6 ]
Wasim, Syed [4 ,5 ,7 ]
Morel, Chantal [4 ,5 ]
Iwanochko, Robert M. [8 ]
Thavendiranathan, Paaladinesh [3 ]
Crean, Andrew Michael [2 ,3 ]
机构
[1] Univ Toronto, St Michaels Hosp, Dept Med Imaging, 30 Bond St, Toronto, ON M5B 1W8, Canada
[2] Univ Toronto, Dept Med Imaging, Peter Munk Cardiac Ctr, Toronto Gen Hosp, 585 Univ Ave, Toronto, ON M5G 2N2, Canada
[3] Univ Toronto, Peter Munk Cardiac Ctr, Toronto Gen Hosp, Div Cardiol, 585 Univ Ave, Toronto, ON M5G 2N2, Canada
[4] Univ Hlth Network, Fred A Litwin Ctr Genet Med, 60 Murray St,3rd Floor,Room 400, Toronto, ON M5T 3L9, Canada
[5] Mt Sinai Hosp, 60 Murray St,3rd Floor,Room 400, Toronto, ON M5T 3L9, Canada
[6] Univ Hong Kong, Dept Diagnost Radiol, Queen Mary Hosp, 102 Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
[7] Hosp Sick Children, 555 Univ Ave, Toronto, ON M5G 1X8, Canada
[8] Toronto Western Hosp, Div Cardiol, 399 Bathurst St, Toronto, ON M5T 2S8, Canada
关键词
Cardiomyopathy; Hypertrophy; Cardiovascular magnetic resonance; Anderson-Fabry disease; Left ventricular morphology; Myocardial scar; Late gadolinium enhancement; LEFT-VENTRICULAR HYPERTROPHY; GALACTOSIDASE-A-GENE; ALPHA-GALACTOSIDASE; PAPILLARY-MUSCLES; ATYPICAL VARIANT; SUDDEN-DEATH; CARDIOMYOPATHY; PREVALENCE; MUTATIONS; MANIFESTATIONS;
D O I
10.1186/s12968-016-0233-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Although it is known that Anderson-Fabry Disease (AFD) can mimic the morphologic manifestations of hypertrophic cardiomyopathy (HCM) on echocardiography, there is a lack of cardiovascular magnetic resonance (CMR) literature on this. There is limited information in the published literature on the distribution of myocardial fibrosis in patients with AFD, with scar reported principally in the basal inferolateral midwall. Methods: All patients with confirmed AFD undergoing CMR at our center were included. Left ventricular (LV) volumes, wall thicknesses and scar were analyzed offline. Patients were categorized into 4 groups: 1) no wall thickening; 2) concentric hypertrophy; 3) asymmetric septal hypertrophy (ASH); and 4) apical hypertrophy. Charts were reviewed for clinical information. Results: Thirty-nine patients were included (20 males [51 %], median age 45.2 years [range 22.3-64.4]). Almost half (17/39) had concentric wall thickening. Almost half (17/39) had pathologic LV scar; three quarters of these (13/17) had typical inferolateral midwall scar. A quarter (9/39) had both concentric wall thickening and typical inferolateral scar. A subgroup with ASH and apical hypertrophy (n = 5) had greater maximum wall thickness, total LV scar, apical scar and mid-ventricular scar than those with concentric hypertrophy (n = 17, p < 0.05). Patients with elevated LVMI had more overall arrhythmia (p = 0.007) more ventricular arrhythmia (p = 0.007) and sustained ventricular tachycardia (p = 0.008). Conclusions: Concentric thickening and inferolateral mid-myocardial scar are the most common manifestations of AFD, but the spectrum includes cases morphologically identical to apical and ASH subtypes of HCM and these have more apical and mid-ventricular LV scar. Significant LVH is associated with ventricular arrhythmia.
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页数:10
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