Effect of High-Intensity Interval Training in De Novo Heart Transplant Recipients in Scandinavia
- PMID: 30773030
- DOI: 10.1161/CIRCULATIONAHA.118.036747
Effect of High-Intensity Interval Training in De Novo Heart Transplant Recipients in Scandinavia
Erratum in
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Correction to: Effect of High-Intensity Interval Training in De Novo Heart Transplant Recipients in Scandinavia: One-Year Follow-Up of the HITTS Randomized, Controlled Study.Circulation. 2019 Oct 22;140(17):e737. doi: 10.1161/CIR.0000000000000739. Epub 2019 Oct 21. Circulation. 2019. PMID: 31634009 No abstract available.
Abstract
Background: There is no consensus on how, when, or at what intensity exercise should be performed after heart transplantation (HTx). We have recently shown that high-intensity interval training (HIT) is safe, well tolerated, and efficacious in the maintenance state after HTx, but studies have not investigated HIT effects in the de novo HTx state. We hypothesized that HIT could be introduced early after HTx and that it could lead to clinically meaningful increases in exercise capacity and health-related quality of life.
Methods: This multicenter, prospective, randomized, controlled trial included 81 patients a mean of 11 weeks (range, 7-16 weeks) after an HTx. Patients were randomized 1:1 to 9 months of either HIT (4×4-minute intervals at 85%-95% of peak effort) or moderate-intensity continuous training (60%-80% of peak effort). The primary outcome was the effect of HIT versus moderate-intensity continuous training on the change in aerobic exercise capacity, assessed as the peak oxygen consumption (Vo2peak). Secondary outcomes included tolerability, safety, adverse events, isokinetic muscular strength, body composition, health-related quality of life, left ventricular function, hemodynamics, endothelial function, and biomarkers.
Results: From baseline to follow-up, 96% of patients completed the study. There were no serious exercise-related adverse events. The population comprised 73% men, and the mean±SD age was 49±13 years. At the 1-year follow-up, the HIT group demonstrated greater improvements than the moderate-intensity continuous training group; the groups showed significantly different changes in the Vo2peak (mean difference between groups, 1.8 mL·kg-1·min-1), the anaerobic threshold (0.28 L/min), the peak expiratory flow (11%), and the extensor muscle exercise capacity (464 J). The 1.8-mL·kg-1·min-1 difference was equal to ≈0.5 metabolic equivalents, which is regarded as clinically meaningful and relevant. Health-related quality of life was similar between the groups, as indicated by results from the Short Form-36 (version 2), Hospital Anxiety and Depression Scale, and a visual analog scale.
Conclusions: We demonstrated that HIT was a safe, efficient exercise method in de novo HTx recipients. HIT, compared with moderate-intensity continuous training, resulted in a clinically significantly greater change in exercise capacity based on the Vo2peak values (25% versus 15%), anaerobic threshold, peak expiratory flow, and muscular exercise capacity.
Clinical trial registration: URL: https://www.clinicaltrials.gov . Unique identifier NCT01796379.
Keywords: exercise test; health-related quality of life; heart transplantation; high-intensity interval training; muscle strength; peak oxygen consumption; safety.
Comment in
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Improving Exercise Capacity in Recent Heart Transplant Recipients.Circulation. 2019 May 7;139(19):2212-2214. doi: 10.1161/CIRCULATIONAHA.119.039845. Circulation. 2019. PMID: 31059321 No abstract available.
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Letter by Haegele et al Regarding Article, "Effect of High-Intensity Interval Training in De Novo Heart Transplant Recipients in Scandinavia".Circulation. 2019 Oct 22;140(17):e733-e734. doi: 10.1161/CIRCULATIONAHA.119.042284. Epub 2019 Oct 21. Circulation. 2019. PMID: 31634010 No abstract available.
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Response by Nytrøen et al to Letter Regarding Article, "Effect of High-Intensity Interval Training in De Novo Heart Transplant Recipients in Scandinavia".Circulation. 2019 Oct 22;140(17):e735-e736. doi: 10.1161/CIRCULATIONAHA.119.042458. Epub 2019 Oct 21. Circulation. 2019. PMID: 31634012 No abstract available.
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