Exercise restriction is protective for genotype-positive family members of arrhythmogenic right ventricular cardiomyopathy patients

Author:

Wang Weijia12ORCID,Tichnell Crystal1,Murray Brittney A1,Agafonova Julia1,Cadrin-Tourigny Julia1,Chelko Stephen1,Tandri Harikrishna1,Calkins Hugh1,James Cynthia A1

Affiliation:

1. Department of Medicine, Division of Cardiology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA

2. Department of Medicine, Division of Cardiology, University of Massachusetts School of Medicine, Worcester, MA, USA

Abstract

Abstract Aims In arrhythmogenic right ventricular cardiomyopathy (ARVC) patients, exercise worsens disease course, so exercise restriction is recommended. However, recommendations for genotype-positive ARVC family members is incompletely resolved. We aimed to provide evidence for exercise recommendations for genotype-positive ARVC family members. Methods and results Arrhythmogenic right ventricular cardiomyopathy family members inheriting a pathogenic desmosomal variant were interviewed about exercise history from age 10. Exercise was characterized by duration, intensity, and dose (duration*intensity). Associations between exercise and (i) diagnosis by 2010 Task Force Criteria and (ii) development of sustained ventricular arrhythmias were examined. The study included 101 family members (age: 40.5 ± 19.3 years, male: 41%, Plakophilin-2 variant: 81%). Forty-four individuals (44%) met diagnostic criteria and 16 (16%) experienced sustained ventricular arrhythmia. Individuals who met diagnostic criteria had significantly higher average exercise duration and dose, but not peak intensity than those who did not. Only one individual who exercised below the American Heart Association recommended minimum (650 metabolic equivalent of task-hours/year) met diagnostic criteria or experienced sustained ventricular arrhythmia as opposed to 50% of individuals who exceeded it (adjusted odds ratio = 0.03, 95% confidence interval 0.003–0.26). The difference in exercise exposure between affected and unaffected individuals was more striking in females than in males. Females who had done high-dose exercise in adolescence had the worst survival free from diagnosis (P < 0.01). Conclusions In phenotype-negative ARVC family members with a pathogenic desmosomal variant, athletic activities should be limited, particularly exercise dose. Exercise may play a greater role in promoting disease in female family members.

Funder

Fondation Leducq

Leonie-Wild Foundation

Dr Francis P. Chiaramonte Private Foundation

Leyla Erkan Family Fund for ARVD Research

Dr Satish, Rupal

Robin Shah ARVD Fund

Bogle Foundation

Healing Hearts Foundation

Campanella family

Patrick J. Harrison Family

Peter French Memorial Foundation

Wilmerding Endowments

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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