University of Alberta, Edmonton, Alberta, Canada.
Karolinska Institutet, Stockholm, Sweden.
Am J Kidney Dis. 2014 Feb;63(2):268-75. doi: 10.1053/j.ajkd.2013.06.010. Epub 2013 Jul 26.
Studies linking low serum testosterone concentration to adverse clinical outcomes in hemodialysis patients have been relatively small. We investigated the role of testosterone in adverse outcomes and quality of life in an incident cohort of male Canadian hemodialysis patients.
A prospectively designed multicenter observational study using data from the Canadian Kidney Disease Cohort Study (CKDCS).
SETTING & PARTICIPANTS: Male patients initiating hemodialysis therapy since February 14, 2005, in 3 Canadian centers serving ethnically diverse populations were studied (N = 623).
Serum testosterone levels using the International Society of Andrology, International Society for the Study of the Aging Male, and European Association of Urology cutoffs (low, <231 ng/dL; borderline, 231-346 ng/dL; normal, >346 ng/dL).
All-cause mortality, fatal and nonfatal cardiovascular (CV) events, and Health Utility Index (HUI)-assessed health-related quality of life.
Participants completed a structured interview on demographics and medical history and an HUI questionnaire (version 3). Routine laboratory test results captured into the study database, and serum testosterone measured within 3 months after initiation of the baseline hemodialysis session.
During a median follow-up of 20 (range, 1-81) months, 166 (27%) died and 98 (20%) had a CV event. Mean serum testosterone level was 234.1 ± 146.1 (SD) ng/dL. Higher serum testosterone levels were associated with significantly decreased unadjusted risk of death (HR per 10-ng/dL increase, 0.58; 95% CI, 0.37-0.90). There was a statistically significant trend for higher all-cause mortality with low serum testosterone levels in adjusted analyses (P < 0.001). Higher levels of log-transformed testosterone were associated with significantly higher HUI scores (P for trend <0.001), and low levels of serum testosterone were associated significantly with lower HUI scores (P for trend <0.001). Although there was a significant trend in the unadjusted risk of CV events among participants with low serum testosterone levels (P < 0.001), the risk was no longer significant after adjustment for age. There was no significant interaction with age and serum testosterone level tested as continuous variables (P = 0.07).
A short follow-up period and serum testosterone measured on a single occasion.
Low serum testosterone concentration may be a modifiable risk factor for adverse outcomes and poor quality of life in male hemodialysis patients. This hypothesis should be tested in randomized controlled trials.
将低血清睾丸激素浓度与血液透析患者的不良临床结局联系起来的研究相对较少。我们调查了睾丸激素在加拿大血液透析患者队列中的作用不良结局和生活质量。
这是一项前瞻性设计的多中心观察性研究,使用了加拿大肾脏疾病队列研究(CKDCS)的数据。
2005 年 2 月 14 日以来,在加拿大 3 个为不同种族人群服务的中心开始血液透析治疗的男性患者(N=623)。
使用国际男科协会、国际老年男性研究学会和欧洲泌尿外科学会的标准(低,<231ng/dL;边缘,231-346ng/dL;正常,>346ng/dL)测量血清睾丸激素水平。
全因死亡率、致命和非致命心血管(CV)事件以及健康效用指数(HUI)评估的健康相关生活质量。
参与者完成了关于人口统计学和病史的结构化访谈以及 HUI 问卷(第 3 版)。研究数据库中捕获了常规实验室检测结果,并在基线血液透析疗程开始后 3 个月内测量了血清睾丸激素。
在中位数为 20 个月(范围,1-81)的随访期间,166 人(27%)死亡,98 人(20%)发生心血管事件。平均血清睾丸激素水平为 234.1±146.1(SD)ng/dL。较高的血清睾丸激素水平与未调整死亡风险显著降低相关(每增加 10ng/dL,HR 为 0.58;95%CI,0.37-0.90)。在调整分析中,低血清睾丸激素水平与全因死亡率呈统计学显著趋势(P<0.001)。较高水平的对数转换睾丸激素与 HUI 评分显著升高相关(趋势 P<0.001),而低水平的血清睾丸激素与 HUI 评分显著降低相关(趋势 P<0.001)。虽然在未调整的低血清睾丸激素水平参与者的 CV 事件风险中存在显著趋势(P<0.001),但在调整年龄后,该风险不再显著。未发现年龄和血清睾丸激素水平作为连续变量的交互作用(P=0.07)。
随访时间短,单次测量血清睾丸激素。
低血清睾丸激素浓度可能是男性血液透析患者不良结局和生活质量差的可改变危险因素。这一假设应在随机对照试验中进行检验。