4.5 Article

Integrating Exercise Into Personalized Ventricular Arrhythmia Risk Prediction in Arrhythmogenic Right Ventricular Cardiomyopathy

期刊

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCEP.121.010221

关键词

arrhythmogenic right ventricular dysplasia; exercise; prognosis

资金

  1. Dutch Heart Foundation [CVON2015-12 eDetect, 2018-30 PREDICT2, 2015T058]
  2. European Union [680969]
  3. Leonie-Wild Foundation
  4. Dr Francis P. Chiaramonte Private Foundation
  5. Leyla Erkan Family Fund
  6. Dr Satish, Rupal and Robin Shah ARVD Fund
  7. Bogle Foundation
  8. Healing Hearts Foundation
  9. Campanella Family, Patrick J. Harrison Family, Peter French Memorial Foundation
  10. Wilmerding Endowments [UL1 TR003098]
  11. UCL Hospitals NIHR Biomedical Research Center
  12. H2020 Societal Challenges Programme [680969] Funding Source: H2020 Societal Challenges Programme

向作者/读者索取更多资源

Exercise at diagnosis was found to be dose-dependently associated with the risk of sustained ventricular arrhythmias in patients with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), but only above a certain threshold. Adding athlete status to the ARVC risk calculator did not improve its accuracy.
BACKGROUND: Exercise is associated with sustained ventricular arrhythmias (VA) in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) but is not included in the ARVC risk calculator (arvcrisk.com). The objective of this study is to quantify the influence of exercise at diagnosis on incident VA risk and evaluate whether the risk calculator needs adjustment for exercise. METHODS: We interviewed ARVC patients without sustained VA at diagnosis about their exercise history. The relationship between exercise dose 3 years preceding diagnosis (average METh/wk) and incident VA during follow-up was analyzed with time-to-event analysis. The incremental prognostic value of exercise to the risk calculator was evaluated by Cox models. RESULTS: We included 176 patients (male, 43.2%; age, 37.6 +/- 16.1 years) from 3 ARVC centers, of whom 53 (30.1%) developed sustained VA during 5.4 (2.7-9.7) years of follow-up. Exercise at diagnosis showed a dose-dependent nonlinear relationship with VA, with no significant risk increase <15 to 30 METh/wk. Athlete status, using 3 definitions from literature (>18, >24, and >36 METh/wk), was significantly associated with VA (hazard ratios, 2.53-2.91) but was also correlated with risk factors currently in the risk calculator model. Thus, adding athlete status to the model did not change the C index of 0.77 (0.71-0.84) and showed no significant improvement (Akaike information criterion change, <2). CONCLUSIONS: Exercise at diagnosis was dose dependently associated with risk of sustained VA in ARVC patients but only above 15 to 30 METh/wk. Exercise does not appear to have incremental prognostic value over the risk calculator. The ARVC risk calculator can be used accurately in athletic patients without modification.

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