Background-To prospectively evaluate whether short-term high-intensity (interval) training (HI(I)T) induces detectable morphological cardiac changes in previously untrained men in cardiovascular magnetic resonance imaging. Methods and Results-Eighty-four untrained volunteers were randomly assigned to a HI(I) T group (n=42; 44.1±4.7 years) or an inactive control group (n=42; 42.3±5.6 years). HI(I)T focused on interval runs (intensity: 95%-105% of individually calculated heart rate at the anaerobic threshold). Before and after 16 weeks, all subjects underwent physiological examination, stepwise treadmill test with blood lactate analysis, and contrast-enhanced cardiovascular magnetic resonance imaging (cine, tagging, and delayed enhancement). Indexed left ventricular (LV) and right ventricular (RV) volume (LV, 77.1±8.5-83.9±8.6; RV, 80.5±8.5-86.6±8.1) and mass (LV, RV,.1) significantly increased with HI(I)T. Changes in LV and RV morphological parameters with HI(I)T were highly correlated with an increase in maximal aerobic capacity (VO 2max ) and a decrease in blood lactate concentration at the anaerobic threshold. Mean LV and RV remodeling index of HI(I)T group did not alter with training (0.76 ±0.09 and 0.24±0.10 g/mL, respectively [P=0. 97 and P=0.72]), indicating balanced cardiac adaptation. Myocardial circumferential strain decreased after HI(I)T within all 6 basal segments (anteroseptal, P=0.01 and anterolateral, P<0.001). There was no late gadolinium enhancement in any of the participants before or post HI(I)T.
Conclusions-Sixteen
Scharf et al Cardiac Adaptation to HI(I)Tinvestigations revealed enlargement and reduced contractility of the RV, which might be associated with ventricular tachycardia.
15The Running Study and Heart (RUSH) trial was designed to address these issues. Physiological and morphological data were collected and cardiopulmonary exercise testing with blood lactate analysis as well as CMR imaging was performed in a randomized controlled trial.
Methods
Study PopulationThe study (www.clinicaltrials.gov, NCT01406730) was approved by the institutional review board and written informed consent was obtained from all subjects. Sample size was determined with G*power (version 3.1.3; 2009, Faul et al,16 Dusseldorf, Germany). We estimated that a sample size of 32 individuals in each group would have a power of 90% to detect a between-group difference of 8±10 mL in end-diastolic volume (EDV) with α=0.05. Assuming a dropout rate of 20%, our goal was to recruit 40 subjects per group. Study subjects were recruited by local newspaper advertisement from January until March 2011. The study was conducted from April 2011 until July 2012. Participants were randomly assigned to a training and restgroup.Eighty-eight male volunteers, who were either completely sedentary or did not engage in any routine (ie, >3 hours per week) physical training, were enrolled in this study. All participants completed a medical history and physical activity questionnaire. All subjects denied the use of illicit substances and un...