The Guenther Dermatology Research Centre, London, ON, Canada.
J Eur Acad Dermatol Venereol. 2011 Jul;25(7):851-7. doi: 10.1111/j.1468-3083.2011.04082.x. Epub 2011 Apr 27.
Ustekinumab, a human anti-interleukin-12/23 monoclonal antibody, has been shown to effectively treat moderate-to-severe psoriasis which significantly affects health-related quality of life (HRQoL), including patients' sexual lives.
The aim of this study was to determine if sexual difficulties associated with psoriasis are related to disease severity and whether sexual difficulties improve with skin disease during ustekinumab treatment.
In phase III PHOENIX 1 and 2 trials, psoriasis patients were randomized to ustekinumab (n=1334) at weeks 0 and 4 and q12 weeks thereafter or placebo (n=662) at weeks 0 and 4 with crossover to ustekinumab at week 12. Psoriasis Area and Severity Index (PASI) and Dermatology Life Quality Index (DLQI) were used to assess psoriasis severity and patient-reported HRQoL respectively. Based on DLQI Question #9, impaired sexual function was defined as 'very much' or 'a lot' of sexual difficulties.
At baseline, mean DLQI was 12.0, indicating a very large negative effect on patients' lives. Impaired sexual function was reported by 22.6% (women=27.1%; men=20.8%) and was significantly associated with increased psoriasis severity. At week 12, ustekinumab-treated patients had a greater mean improvement in DLQI (-9.13 vs. -0.53 with placebo, P<0.001) and the proportion of patients with impaired sexual function decreased from 22.4% to 2.7% compared with no change with placebo (P<0.001). Patients with greater PASI improvement experienced a greater reduction of sexual difficulties due to psoriasis. A similar pattern of improved sexual function was observed at weeks 24-28 in placebo crossover patients.
Ustekinumab treatment is associated with significant improvement in HRQoL and sexual difficulties due to psoriasis.
乌司奴单抗是一种人源抗白细胞介素-12/23 单克隆抗体,已被证实能有效治疗中重度银屑病,显著改善与健康相关的生活质量(HRQoL),包括患者的性生活。
本研究旨在确定与银屑病相关的性困难是否与疾病严重程度有关,以及乌司奴单抗治疗期间皮肤疾病改善是否会改善性困难。
在 III 期 PHOENIX 1 和 2 试验中,银屑病患者被随机分配至乌司奴单抗(n=1334)组,在第 0 和 4 周时给药,此后每 12 周给药一次,或安慰剂(n=662)组,在第 0 和 4 周时给药,在第 12 周时交叉至乌司奴单抗组。使用银屑病面积和严重程度指数(PASI)和皮肤病生活质量指数(DLQI)分别评估银屑病严重程度和患者报告的 HRQoL。根据 DLQI 问题 #9,受损的性功能定义为“非常”或“很多”的性困难。
基线时,平均 DLQI 为 12.0,表明对患者生活有非常大的负面影响。22.6%(女性=27.1%;男性=20.8%)报告存在受损的性功能,与银屑病严重程度增加显著相关。在第 12 周时,乌司奴单抗治疗患者的 DLQI 平均改善更大(-9.13 与安慰剂组的-0.53,P<0.001),并且存在受损性功能的患者比例从 22.4%降至 2.7%,而安慰剂组无变化(P<0.001)。PASI 改善更大的患者因银屑病导致的性困难减少幅度更大。在安慰剂交叉患者中,在第 24-28 周时也观察到类似的性功能改善模式。
乌司奴单抗治疗与因银屑病导致的 HRQoL 和性功能显著改善相关。