Rabkin J G, Wagner G J, Rabkin R
New York State Psychiatric Institute, Department of Psychiatry, College of Physicians and Surgeons, Columbia University, New York 10032, USA.
Arch Gen Psychiatry. 2000 Feb;57(2):141-7; discussion 155-6. doi: 10.1001/archpsyc.57.2.141.
The goal was to evaluate the efficacy of testosterone in alleviation of hypogonadal symptoms (diminished libido, depressed mood, low energy, and depleted muscle mass) in men with symptomatic human immunodeficiency virus illness.
Seventy-four patients were enrolled in a double-blind, placebo-controlled 6-week trial with bi-weekly testosterone injections, followed by 12 weeks of open-label maintenance treatment. Major outcome measures were Clinical Global Impressions Scale ratings for libido, mood, energy, and erectile function; Hamilton Depression Rating Scale scores, and Chalder Fatigue Scale scores. Body composition changes were assessed with bioelectric impedance analysis.
Seventy men completed the 6-week trial. Response rates, defined as much or very much improved libido, were 74% (28/38) for patients randomized to testosterone, and 19% (6/32) for placebo-treated patients (P<.001). Of the 62 completers with fatigue at baseline, 59% (20/34) receiving testosterone and 25% (7/28) receiving placebo reported improved energy (P<.01). Among the 26 completers with an Axis I depressive disorder at baseline, 58% of the testosterone-treated patients reported improved mood compared with 14% of placebo-treated patients (Fisher exact test = .08). With testosterone treatment, average increase in muscle mass over 12 weeks was 1.6 kg for the whole group, and 2.2 kg for the 14 men with wasting at baseline. Improvement on all parameters was maintained during subsequent open-label treatment for up to 18 weeks.
Testosterone is well tolerated and effective in the short-term treatment of symptoms of clinical hypogonadism in men with symptomatic human immunodeficiency virus illness, restoring libido and energy, alleviating depressed mood, and increasing muscle mass.
目的是评估睾酮对有症状的人类免疫缺陷病毒感染男性性腺功能减退症状(性欲减退、情绪低落、精力不足和肌肉量减少)的缓解效果。
74名患者参加了一项双盲、安慰剂对照的6周试验,每两周注射一次睾酮,随后进行12周的开放标签维持治疗。主要结局指标包括性欲、情绪、精力和勃起功能的临床总体印象量表评分;汉密尔顿抑郁量表得分和查尔德疲劳量表得分。采用生物电阻抗分析评估身体成分变化。
70名男性完成了6周试验。随机接受睾酮治疗的患者中,性欲改善程度为“改善很多”或“改善非常多”的反应率为74%(28/38),而接受安慰剂治疗的患者为19%(6/32)(P<0.001)。在62名基线时有疲劳症状的完成试验者中,接受睾酮治疗的患者中有59%(20/34)报告精力有所改善,接受安慰剂治疗的患者中有25%(7/28)报告精力改善(P<0.01)。在26名基线时有轴I型抑郁症的完成试验者中,接受睾酮治疗的患者中有58%报告情绪改善,而接受安慰剂治疗的患者中这一比例为14%(Fisher精确检验P=0.08)。接受睾酮治疗后,整个组在12周内肌肉量平均增加1.6千克,基线时有消瘦的14名男性平均增加2.2千克。在随后长达18周的开放标签治疗期间,所有参数的改善情况均得以维持。
睾酮耐受性良好,对有症状的人类免疫缺陷病毒感染男性临床性腺功能减退症状的短期治疗有效,可恢复性欲和精力,缓解情绪低落,并增加肌肉量。