Thiago Gagliano-Jucá, Tevhide Betul Icli, K. Pencina, Zhuoying Li, J. Tapper, Grace Huang, T. Travison, P. Tsitouras, S. Harman, T. Storer, S. Bhasin, S. Basaria
{"title":"Effects of Testosterone Replacement on Electrocardiographic Parameters in Men: Findings From Two Randomized Trials","authors":"Thiago Gagliano-Jucá, Tevhide Betul Icli, K. Pencina, Zhuoying Li, J. Tapper, Grace Huang, T. Travison, P. Tsitouras, S. Harman, T. Storer, S. Bhasin, S. Basaria","doi":"10.1210/jc.2016-3669","DOIUrl":null,"url":null,"abstract":"Context\nEndogenous testosterone levels have been negatively associated with QTc interval in small case series; the effects of testosterone therapy on electrocardiographic parameters have not been evaluated in randomized trials.\n\n\nObjective\nTo evaluate the effects of testosterone replacement on corrected QT interval (QTcF) in two randomized controlled trials.\n\n\nParticipants\nMen with pre- and postrandomization electrocardiograms (ECGs) from the Testosterone and Pain (TAP) and the Testosterone Effects on Atherosclerosis in Aging Men (TEAAM) Trials.\n\n\nInterventions\nParticipants were randomized to either placebo or testosterone gel for 14 weeks (TAP) or 36 months (TEAAM). ECGs were performed at baseline and at the end of interventions in both trials; in the TEAAM trial ECGs were also obtained at 12 and 24 months.\n\n\nOutcomes\nDifference in change in the QTcF between testosterone and placebo groups was assessed in each trial. Association of changes in testosterone levels with changes in QTcF was analyzed in men assigned to the testosterone group of each trial.\n\n\nResults\nMean total testosterone levels increased in the testosterone group of both trials. In the TAP trial, there was a nonsignificant reduction in mean QTcF in the testosterone group compared with placebo (effect size = -4.72 ms; P = 0.228) and the changes in QTcF were negatively associated to changes in circulating testosterone (P = 0.036). In the TEAAM trial, testosterone attenuated the age-related increase in QTcF seen in the placebo group (effect size= -6.30 ms; P < 0.001).\n\n\nConclusion\nTestosterone replacement attenuated the age-related increase in QTcF duration in men. The clinical implications of these findings require further investigation.","PeriodicalId":22632,"journal":{"name":"The Journal of Clinical Endocrinology & Metabolism","volume":"161 1","pages":"1478–1485"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"17","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Clinical Endocrinology & Metabolism","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1210/jc.2016-3669","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 17
Abstract
Context
Endogenous testosterone levels have been negatively associated with QTc interval in small case series; the effects of testosterone therapy on electrocardiographic parameters have not been evaluated in randomized trials.
Objective
To evaluate the effects of testosterone replacement on corrected QT interval (QTcF) in two randomized controlled trials.
Participants
Men with pre- and postrandomization electrocardiograms (ECGs) from the Testosterone and Pain (TAP) and the Testosterone Effects on Atherosclerosis in Aging Men (TEAAM) Trials.
Interventions
Participants were randomized to either placebo or testosterone gel for 14 weeks (TAP) or 36 months (TEAAM). ECGs were performed at baseline and at the end of interventions in both trials; in the TEAAM trial ECGs were also obtained at 12 and 24 months.
Outcomes
Difference in change in the QTcF between testosterone and placebo groups was assessed in each trial. Association of changes in testosterone levels with changes in QTcF was analyzed in men assigned to the testosterone group of each trial.
Results
Mean total testosterone levels increased in the testosterone group of both trials. In the TAP trial, there was a nonsignificant reduction in mean QTcF in the testosterone group compared with placebo (effect size = -4.72 ms; P = 0.228) and the changes in QTcF were negatively associated to changes in circulating testosterone (P = 0.036). In the TEAAM trial, testosterone attenuated the age-related increase in QTcF seen in the placebo group (effect size= -6.30 ms; P < 0.001).
Conclusion
Testosterone replacement attenuated the age-related increase in QTcF duration in men. The clinical implications of these findings require further investigation.