Phenotypic Manifestations of Arrhythmogenic Cardiomyopathy in Children and Adolescents

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

卷:74

Article

DeWitt, Elizabeth S.^1,2  Chandler, Stephanie F.^1,2  Hylind, Robyn J.^1,2  Ladouceur, Virginie Beausejour^1,2  Blume, Elizabeth D.²  VanderPluym, Christina²  Powell, Andrew J.²  Fynn-Thompson, Francis³  Roberts, Amy E.²  Sanders, Stephen P.^2,4  Bezzerides, Vassilios^1,2  Lakdawala, Neal K.⁵  MacRae, Calum A.⁵  Abrams, Dominic J.^1,2 

[1] Harvard Med Sch, Boston Childrens Hosp, Inherited Cardiac Arrhythmia Program, Boston, MA 02115 USA

[2] Harvard Med Sch, Boston Childrens Hosp, Dept Cardiol, Boston, MA 02115 USA

[3] Harvard Med Sch, Boston Childrens Hosp, Dept Cardiovasc Surg, Boston, MA 02115 USA

[4] Harvard Med Sch, Boston Childrens Hosp, Dept Pathol, Boston, MA 02115 USA

[5] Harvard Med Sch, Brigham & Womens Hosp, Div Cardiovasc Med, Cardiovasc Genet Program, Boston, MA 02115 USA

关键词: arrhythmogenic right;    ventricular cardiomyopathy;    desmosomes;    diagnostic criteria;    genetics;    pediatrics;    phenotype;   

DOI  :  10.1016/j.jacc.2019.05.022

来源: Elsevier

【 摘 要 】

BACKGROUND Arrhythmogenic cardiomyopathy (ACM) is a variably penetrant disease increasingly identified in young patients. OBJECTIVES This study sought to describe the diverse phenotype, genotype, and outcomes in pediatric and adolescent patients. METHODS Records from 1999 to 2016 were reviewed for individuals age <21 years with a consistent personal or family history. Patients were categorized by right ventricular (RV), left dominant (LD), or biventricular subtypes using 2010 Task Force Criteria or proposed features of LD disease, encompassing electrocardiographic, structural, histological, and arrhythmic characteristics. Genetic variants classified as pathogenic and/or likely pathogenic by 2015 American College of Medical Genetics and Genomics criteria in recognized disease-associated genes were included. RESULTS Manifest disease was evident in 32 patients (age 15.1 +/- 3.8 years), of whom 22 were probands, including 16 RV, 7 LD, and 9 biventricular ACM. Nondiagnostic features were seen in 5 of 15 family members. RV disease was associated with cardiac arrest and ventricular tachycardia (p = 0.02) and prevalence of PKP2 variants (p < 0.01), whereas biventricular disease was associated with a younger age of onset (p = 0.02). LD ACM was associated with variants in DSP and LMNA, and biventricular ACM with more a diverse etiology in desmosomal genes. Cardiac arrest was observed in 5 probands (age 15.3 +/- 1.9 years) and ventricular tachycardia in 10 (age 16.6 +/- 2.7 years), 6 probands, and 4 family members. Features suggestive of myocardial inflammation were seen in 6 patients, with ventricular tachycardia and/or cardiac arrest in 3 patients. Cardiac transplantation was performed in 10 patients. There were no deaths. In RV and biventricular disease, electrocardiographic preceded imaging features, whereas the reverse was seen in LD disease. CONCLUSIONS ACM in the young has highly varied phenotypic expression incorporating life-threatening arrhythmia, heart failure, and myocardial inflammation. Increased awareness of early onset, aggressive disease has important implications for patient management and familial screening. (C) 2019 by the American College of Cardiology Foundation.

【 授权许可】

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