Effects of high-intensity interval training on platelet function in cardiac rehabilitation: a randomised controlled trial

医学 间歇训练 内科学 高强度间歇训练 心脏病学 血小板 有氧运动 血小板活化
作者
Stefan Heber,Beatrix Fischer,Marina Sallaberger‐Lehner,Maria Hausharter,Helmuth Ocenasek,Andreas Gleiß,Michael J. M. Fischer,Rochus Pokan,Alice Assinger,Ivo Volf
出处
期刊:Heart [BMJ]
卷期号:106 (1): 69-79 被引量:9
标识
DOI:10.1136/heartjnl-2019-315130
摘要

Objective To compare effects of moderate-intensity continuous training (MICT) and high-intensity interval training (HIIT) on platelet function in patients undergoing cardiac rehabilitation, as hyper-reactive platelets are involved in atherogenesis and atherothrombosis. Methods In this single-centre parallel group randomised controlled trial, male patients after an acute coronary syndrome under dual antiplatelet therapy performed MICT or HIIT+MICT for 12 weeks. Main outcome was platelet reactivity measured by the half-maximal concentration (EC 50 ) of platelet agonist thrombin receptor-activating peptide-6 (TRAP-6) in terms of P-selectin expression. EC 50 was determined at baseline, after 6 and 12 weeks, each time at physical rest and on exertion. Results 82 patients were randomised to MICT or HIIT+MICT. Mean (95% CI) baseline EC 50 values at physical rest were 6.7 µM (6.3 µM to 7.0 µM) TRAP-6. After 6/12 weeks, 36/33 MICT and 34/28 HIIT+MICT patients were examined. HIIT+MICT patients had 0.9 µM (0.4 µM to 1.4 µM)/0.5 µM (−0.1 µM to 1.0 µM) higher EC 50 values than MICT ones, and the propensity of their platelets to form aggregates with monocytes was significantly lower after 12 weeks. Short-term strenuous physical exertion was generally associated with platelet activation and an EC 50 reduction of 0.7 µM (0.6 µM to 0.8 µM). HIIT+MICT patients tended to be fitter after 12 weeks. No serious harms were observed. Conclusions Including HIIT in cardiac rehabilitation seems to confer additional benefits compared with MICT alone, which should be confirmed in clinical trials with hard endpoints. Exertion-induced platelet activation and hyper-reactivity occur despite dual antiplatelet therapy. Trial registration number NCT02930330 ; Results.

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