Mulligan Kathleen, Zackin Robert, Clark Rebecca A, Alston-Smith Beverly, Liu Tun, Sattler Fred R, Delvers Thomas B, Currier Judith S
Division of Endocrinology, San Francisco General Hospital, 1001 Potrero Avenue, Rm. 3501K, San Francisco, CA 94110, USA.
Arch Intern Med. 2005 Mar 14;165(5):578-85. doi: 10.1001/archinte.165.5.578.
Weight loss is associated with accelerated mortality and disease progression in patients with human immunodeficiency virus (HIV) infection. Although studies have examined a variety of anabolic therapies in HIV-infected men, the safety and efficacy of such treatments in women have not been adequately studied.
In this randomized, double-blind, placebo-controlled, multicenter, phase I/II study, 38 HIV-infected women with documented weight loss of 5% or greater in the preceding year or a body mass index of less than 20 kg/m(2) were randomized to receive nandrolone decanoate (100 mg) or an equivalent volume of placebo every other week by intramuscular injection. Subjects received blinded treatment for 12 weeks, followed by open-label therapy for 12 weeks. Lean body mass and fat (bioelectrical impedance analysis) and weight were measured at baseline and at weeks 6, 12, 18, and 24. Biochemical assessments of safety (hematologic analyses, liver function tests, and sex hormone measurements) were performed at these same time points. Clinical signs and symptoms were monitored biweekly.
Subjects randomized to receive nandrolone had significant increases in weight and lean body mass during blinded treatment (4.6 kg [9.0%] and 3.5 kg [8.6%], respectively; P<.001 vs baseline and placebo in each case). Fat mass did not change statistically significantly in either group. Although there were no statistically significant differences between groups in biochemical measures, the number of grade 3 or greater toxicities, or reports of virilizing effects, a full assessment of safety cannot be made in a trial of this size.
Nandrolone decanoate therapy may prove to be generally safe and beneficial in reversing weight loss and lean tissue loss in women with HIV infection and other chronic catabolic diseases.
体重减轻与人类免疫缺陷病毒(HIV)感染患者的死亡率加速和疾病进展相关。尽管已有研究对感染HIV的男性使用的多种合成代谢疗法进行了研究,但此类治疗方法在女性中的安全性和有效性尚未得到充分研究。
在这项随机、双盲、安慰剂对照、多中心的I/II期研究中,38名HIV感染女性,她们在前一年体重下降达5%或更多,或体重指数低于20kg/m²,被随机分组,通过肌肉注射每两周接受一次癸酸诺龙(100mg)或等量的安慰剂。受试者接受12周的盲法治疗,随后是12周的开放标签治疗。在基线以及第6、12、18和24周测量去脂体重和脂肪(生物电阻抗分析)以及体重。在这些相同时间点进行安全性的生化评估(血液学分析、肝功能测试和性激素测量)。每两周监测临床体征和症状。
随机接受癸酸诺龙的受试者在盲法治疗期间体重和去脂体重显著增加(分别增加4.6kg[9.0%]和3.5kg[8.6%];与基线和安慰剂相比,每组P<0.001)。两组的脂肪量均无统计学上的显著变化。尽管两组在生化指标、3级或更高级别的毒性数量或男性化效应报告方面无统计学上的显著差异,但在如此规模的试验中无法进行全面的安全性评估。
癸酸诺龙疗法在逆转HIV感染女性和其他慢性分解代谢疾病患者的体重减轻和瘦组织丢失方面可能被证明总体上是安全且有益的。