Antoniou Tony, Raboud Janet M, Kovacs Colin, Diong Christina, Brunetta Jason, Smith Graham, Halpenny Roberta, Beninger Francis, Loutfy Mona R
Canadian Immunodeficiency Research Collaborative, Canada.
AIDS Care. 2009 Oct;21(10):1247-52. doi: 10.1080/09540120902814379.
The long-term safety and efficacy of products used in the correction of HIV-associated facial lipoatrophy (FLA) are largely unknown. The purpose of this study was to describe the long-term efficacy and safety of polyalkylimide gel (PAIG) in the treatment of HIV-associated FLA. In this open-label, randomized, single-center study, 31 HIV-positive individuals (median age 48 years (interquartile ranges (IQR) 45, 55, 97% male) with FLA were randomized to immediate (week 0 and six) or delayed (week 12 and 18) PAIG injections. Week 96 endpoints included change in FLA severity scores (FLSS) (five-point scale), proportion of patients with adverse events, and changes in quality of life, depression and anxiety using validated surveys. Results at week 96 were available for 28 patients. Adverse events, including swelling, redness, bruising and pain, were mild, and resolved after a median of three days following the injection. At week 96, median changes in physician and patient FLSS scores were -2 (IQR -3, -1; p<0.001 vs. baseline) and -2 (IQR -2, -1; p<0.001 vs. baseline), respectively. Physician and patient FLSS scores were not significantly different between the groups at week 96. Significant improvements in patient's anxiety (p<0.001), depression (p<0.001) and mental health (p=0.01) were observed from baseline to week 96. In conclusion, treatment with PAIG was associated with sustained improvements in both the physical and psychological components of FLA through 96 weeks of follow-up.
用于矫正与HIV相关的面部脂肪萎缩(FLA)的产品的长期安全性和有效性在很大程度上尚不清楚。本研究的目的是描述聚烷基酰亚胺凝胶(PAIG)治疗与HIV相关的FLA的长期有效性和安全性。在这项开放标签、随机、单中心研究中,31名患有FLA的HIV阳性个体(中位年龄48岁(四分位间距(IQR)45,55,97%为男性)被随机分为即刻(第0周和第6周)或延迟(第12周和第18周)PAIG注射组。第96周的终点包括FLA严重程度评分(FLSS)(五分制)的变化、不良事件患者的比例,以及使用经过验证的调查评估的生活质量、抑郁和焦虑的变化。28名患者有第96周的结果。不良事件包括肿胀红肿、瘀伤和疼痛,均较轻微,注射后中位三天后消退。在第96周,医生和患者的FLSS评分中位数变化分别为-2(IQR -3,-1;与基线相比p<0.001)和-2(IQR -2,-1;与基线相比p<0.001)。第96周时两组之间医生和患者的FLSS评分无显著差异。从基线到第96周,观察到患者的焦虑(p<0.001)、抑郁(p<0.001)和心理健康(p=0.01)有显著改善。总之,通过96周的随访,PAIG治疗与FLA的身体和心理方面的持续改善相关。