Layton J Bradley, Meier Christoph R, Sharpless Julie L, Stürmer Til, Jick Susan S, Brookhart M Alan
Department of Epidemiology, The University of North Carolina at Chapel Hill.
Department of Pharmaceutical Sciences, Basel University, Basel, Switzerland.
JAMA Intern Med. 2015 Jul;175(7):1187-96. doi: 10.1001/jamainternmed.2015.1573.
Increases in testosterone use and mixed reports of adverse events have raised concerns about the cardiovascular safety of testosterone. Testosterone is available in several delivery mechanisms with varying pharmacokinetics; injections cause spikes in testosterone levels, and transdermal patches and gels cause more subtle but sustained increases. The comparative cardiovascular safety of gels, injections, and patches has not been studied.
To determine the comparative cardiovascular safety of testosterone injections, patches, and gels.
DESIGN, SETTING, AND PARTICIPANTS: A retrospective cohort study was conducted using administrative claims from a commercially insured (January 1, 2000, to December 31, 2012) and Medicare (January 1, 2007, to December 31, 2010) population in the United States and general practitioner records from the United Kingdom (January 1, 2000, to June 30, 2012). Participants included men (aged ≥18 years) who initiated use of testosterone patches, gels, or injections following 180 days with no testosterone use. Our analysis was conducted from December 11, 2013, to November 12, 2014.
New initiation of a testosterone dosage form, with use monitored for up to 1 year.
Inpatient or outpatient medical records, diagnoses, or claims for cardiovascular and cerebrovascular events including myocardial infarction (MI), unstable angina, stroke, and composite acute event (MI, unstable angina, or stroke); venous thromboembolism (VTE); mortality; and all-cause hospitalization.
We identified 544,115 testosterone initiators between the 3 data sets: 37.4% injection, 6.9% patch, and 55.8% gel. The majority of men in the Medicare cohort were injection initiators (51.2%), most in the US commercially insured population were gel initiators (56.5%), and the UK database included equal proportions of injections and gel users (approximately 41%). With analysis conducted using hazard ratios and 95% CIs, compared with men using gels, injection initiators had higher hazards of cardiovascular events (ie, MI, unstable angina, and stroke) (1.26; 1.18-1.35), hospitalization (1.16; 1.13-1.19), and death (1.34; 1.15-1.56) but not VTE (0.92; 0.76-1.11). Compared with gels, patches did not confer increased hazards of cardiovascular events (1.10; 0.94-1.29), hospitalization (1.04; 1.00-1.08), death (1.02; 0.77-1.33), or VTE (1.08; 0.79-1.47).
Testosterone injections were associated with a greater risk of cardiovascular events, hospitalizations, and deaths compared with gels. Patches and gels had similar risk profiles. However, this study did not assess whether patients met criteria for use of testosterone and did not assess the safety of testosterone among users compared with nonusers of the drug.
睾酮使用的增加以及关于不良事件的混合报告引发了对睾酮心血管安全性的担忧。睾酮有多种给药方式,其药代动力学各不相同;注射会导致睾酮水平飙升,而透皮贴剂和凝胶会引起更细微但持续的升高。凝胶、注射剂和贴剂的心血管安全性比较尚未得到研究。
确定睾酮注射剂、贴剂和凝胶的心血管安全性比较。
设计、地点和参与者:一项回顾性队列研究使用了美国商业保险人群(2000年1月1日至2012年12月31日)和医疗保险人群(2007年1月1日至2010年12月31日)的行政索赔数据,以及英国全科医生记录(2000年1月1日至2012年6月30日)。参与者包括在180天未使用睾酮后开始使用睾酮贴剂、凝胶或注射剂的男性(年龄≥18岁)。我们的分析于2013年12月11日至2014年11月12日进行。
新开始使用一种睾酮剂型,使用情况监测长达1年。
住院或门诊医疗记录、诊断或心血管和脑血管事件的索赔,包括心肌梗死(MI)、不稳定型心绞痛、中风和复合急性事件(MI、不稳定型心绞痛或中风);静脉血栓栓塞(VTE);死亡率;以及全因住院。
我们在3个数据集中识别出544,115名开始使用睾酮的人:37.4%为注射剂使用者,6.9%为贴剂使用者,55.8%为凝胶使用者。医疗保险队列中的大多数男性是注射剂使用者(51.2%),美国商业保险人群中的大多数是凝胶使用者(56.5%),英国数据库中注射剂和凝胶使用者的比例相等(约41%)。通过使用风险比和95%置信区间进行分析,与使用凝胶的男性相比,注射剂使用者发生心血管事件(即MI、不稳定型心绞痛和中风)的风险更高(1.26;1.18 - 1.35)、住院风险更高(1.16;1.13 - 1.19)和死亡风险更高(1.34;1.15 - 1.56),但VTE风险无差异(0.92;0.76 - 1.11)。与凝胶相比,贴剂使用者发生心血管事件的风险没有增加(1.10;0.94 - 1.29)、住院风险没有增加(1.04;1.00 - 1.08)、死亡风险没有增加(1.02;0.77 - 1.33)或VTE风险没有增加(1.08;0.79 - 1.47)。
与凝胶相比,睾酮注射剂与更高的心血管事件、住院和死亡风险相关。贴剂和凝胶的风险特征相似。然而,本研究未评估患者是否符合使用睾酮的标准,也未评估与未使用该药物的人群相比,使用者中睾酮的安全性。