Journal article
Vigorous Exercise in Patients With Congenital Long-QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study
Circulation (New York, N.Y.), Vol.150(7), pp.516-530
07/25/2024
DOI: 10.1161/CIRCULATIONAHA.123.067590
PMID: 39051104
Abstract
BACKGROUND Whether vigorous exercise increases risk of ventricular arrhythmias for individuals diagnosed and treated for congenital long-QT syndrome (LQTS) remains unknown.The National Institutes of Health-funded LIVE-LQTS study (Lifestyle and Exercise in Genetic Cardiovascular Conditions) prospectively enrolled individuals 8 to 60 years of age with phenotypic or genotypic LQTS from 37 sites in 5 countries from May 2015 to February 2019. Participants (or parents) answered physical activity and clinical events surveys every 6 months for 3 years with follow-up completed in February 2022. Vigorous exercise was defined as ≥6 metabolic equivalents for >60 hours per year. A blinded Clinical Events Committee adjudicated the composite end point of sudden death, sudden cardiac arrest, ventricular arrhythmia treated by an implantable cardioverter defibrillator, and likely arrhythmic syncope. A National Death Index search ascertained vital status for those with incomplete follow-up. A noninferiority hypothesis (boundary of 1.5) between vigorous exercisers and others was tested with multivariable Cox regression analysis.METHODSThe National Institutes of Health-funded LIVE-LQTS study (Lifestyle and Exercise in Genetic Cardiovascular Conditions) prospectively enrolled individuals 8 to 60 years of age with phenotypic or genotypic LQTS from 37 sites in 5 countries from May 2015 to February 2019. Participants (or parents) answered physical activity and clinical events surveys every 6 months for 3 years with follow-up completed in February 2022. Vigorous exercise was defined as ≥6 metabolic equivalents for >60 hours per year. A blinded Clinical Events Committee adjudicated the composite end point of sudden death, sudden cardiac arrest, ventricular arrhythmia treated by an implantable cardioverter defibrillator, and likely arrhythmic syncope. A National Death Index search ascertained vital status for those with incomplete follow-up. A noninferiority hypothesis (boundary of 1.5) between vigorous exercisers and others was tested with multivariable Cox regression analysis.Among the 1413 participants (13% <18 years of age, 35% 18-25 years of age, 67% female, 25% with implantable cardioverter defibrillators, 90% genotype positive, and 49% with LQT1), 91% were treated with beta-blockers, left cardiac sympathetic denervation, or implantable cardioverter defibrillator; 52% participated in vigorous exercise (55% competitively). Thirty-seven individuals experienced the composite end point (including one sudden cardiac arrest and one sudden death in the nonvigorous group, one sudden cardiac arrest in the vigorous group) with overall event rates at 3 years of 2.6% in the vigorous and 2.7% in the nonvigorous exercise groups. The unadjusted hazard ratio for experience of events for the vigorous group compared with the nonvigorous group was 0.97 (90% CI, 0.57-1.67), with an adjusted hazard ratio of 1.17 (90% CI, 0.67-2.04). The upper 95% one-sided confidence level extended beyond the 1.5 boundary. Neither vigorous or nonvigorous exercise was found to be superior in any group or subgroup.RESULTSAmong the 1413 participants (13% <18 years of age, 35% 18-25 years of age, 67% female, 25% with implantable cardioverter defibrillators, 90% genotype positive, and 49% with LQT1), 91% were treated with beta-blockers, left cardiac sympathetic denervation, or implantable cardioverter defibrillator; 52% participated in vigorous exercise (55% competitively). Thirty-seven individuals experienced the composite end point (including one sudden cardiac arrest and one sudden death in the nonvigorous group, one sudden cardiac arrest in the vigorous group) with overall event rates at 3 years of 2.6% in the vigorous and 2.7% in the nonvigorous exercise groups. The unadjusted hazard ratio for experience of events for the vigorous group compared with the nonvigorous group was 0.97 (90% CI, 0.57-1.67), with an adjusted hazard ratio of 1.17 (90% CI, 0.67-2.04). The upper 95% one-sided confidence level extended beyond the 1.5 boundary. Neither vigorous or nonvigorous exercise was found to be superior in any group or subgroup.Among individuals diagnosed with phenotypic or genotypic LQTS who were risk assessed and treated in experienced centers, LQTS-associated cardiac event rates were low and similar between those exercising vigorously and those not exercising vigorously. Consistent with the low event rate, CIs are wide, and noninferiority was not demonstrated. These data further inform shared decision-making discussions between patient and physician about exercise and competitive sports participation. CONCLUSIONS Among individuals diagnosed with phenotypic or genotypic LQTS who were risk assessed and treated in experienced centers, LQTS-associated cardiac event rates were low and similar between those exercising vigorously and those not exercising vigorously. Consistent with the low event rate, CIs are wide, and noninferiority was not demonstrated. These data further inform shared decision-making discussions between patient and physician about exercise and competitive sports participation.URL: https://www.clinicaltrials.gov; Unique identifier: NCT02549664. REGISTRATION URL: https://www.clinicaltrials.gov; Unique identifier: NCT02549664.
Details
- Title: Subtitle
- Vigorous Exercise in Patients With Congenital Long-QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study
- Creators
- Rachel Lampert - Yale UniversitySharlene Day - University of PennsylvaniaBarbara Ainsworth - Arizona State UniversityMatthew Burg - Yale UniversityBradley S Marino - Cleveland ClinicLisa SalbergMaria Teresa Tome Esteban - University of LondonDominic J Abrams - Boston Children's HospitalPeter F Aziz - Cleveland ClinicCheryl Barth - Yale UniversityElijah R Behr - St George's, University of LondonCheyanne Bell - Mayo ClinicCharles I Berul - Children's NationalJohan M Bos - Mayo ClinicDavid Bradley - C. S. Mott Children's HospitalDavid S Cannom - Keck Hospital of USCBryan C Cannon - Mayo ClinicMaryann Anandi Concannon - University of MichiganMarina Cerrone - New York UniversityRichard J Czosek - Cincinnati Children's Hospital Medical CenterAnne M Dubin - Stanford UniversityJames Dziura - Yale UniversityChristopher C Erickson - University of Nebraska Medical CenterN A Mark Estes - Tufts Medical CenterSusan P Etheridge - University of UtahIlan Goldenberg - University of Rochester Medical CenterBelinda Gray - The University of SydneyCarla Haglund-Turnquist - Mayo ClinicKimberly Harmon - University of WashingtonCynthia A James - Johns Hopkins UniversityChristopher Johnsrude - University of LouisvillePrince Kannankeril - Vanderbilt UniversityAlice Lara - Rome FoundationIan H Law - University of IowaFangyong Li - Yale UniversityMark S Link - The University of Texas Southwestern Medical CenterSilvana M Molossi - Texas Children's HospitalBrian Olshansky - University of IowaPeter A Noseworthy - Mayo Clinic in ArizonaElizabeth V Saarel - St. Luke's Children's HospitalShubhayan Sanatani - University of British ColumbiaMaully Shah - Children's Hospital of PhiladelphiaLaura Simone - Yale UniversityJonathan Skinner - Starship Children's HealthGordon F Tomaselli - Albert Einstein College of MedicineJames Simon Ware - Imperial College LondonGregory Webster - Lurie Children's HospitalWojciech Zareba - University of Rochester Medical CenterDouglas P Zipes - Indiana UniversityMichael J Ackerman - Mayo Clinic
- Resource Type
- Journal article
- Publication Details
- Circulation (New York, N.Y.), Vol.150(7), pp.516-530
- DOI
- 10.1161/CIRCULATIONAHA.123.067590
- PMID
- 39051104
- NLM abbreviation
- Circulation
- ISSN
- 1524-4539
- eISSN
- 1524-4539
- Publisher
- LIPPINCOTT WILLIAMS & WILKINS
- Grant note
- National Heart Lung and Blood Institute: 1R01HL125918
This study was funded by National Heart Lung and Blood Institute 1R01HL125918. The funding source had no role in the design and conduct of study, collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; or decision to submit the manuscript for publication.
- Language
- English
- Electronic publication date
- 07/25/2024
- Academic Unit
- Cardiology; Stead Family Department of Pediatrics; Internal Medicine
- Record Identifier
- 9984688451502771
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