Department of Medicine and Immunodeficiency Service, McGill University Health Center, Montreal, Quebec, Canada.
Clin Infect Dis. 2011 May;52(9):1174-81. doi: 10.1093/cid/cir064. Epub 2011 Mar 1.
Human immunodeficiency virus (HIV)-seropositive men who have sex with men (MSM) are at risk for anal intraepithelial neoplasia (AIN) and cancer. The goal of this study was to identify risk factors associated with high-grade AIN (AIN-2,3) in HIV-positive MSM, including the receipt of highly active antiretroviral therapy (HAART).
A cohort study involving 247 HIV-seropositive MSM receiving HAART or initiating HAART was followed up every 6 months for 3 years with human papillomavirus (HPV) testing and high-resolution anoscopy to identify predictors of AIN-2,3 by Cox regression analysis and period prevalence logistic regression.
AIN-2,3 was observed during the study in 132 (53%) of 247 participants. The progression rate to AIN-2,3 from a lesser abnormality at baseline was 12.8 cases per 1000 person-months (95% confidence interval [CI], 9.8-16.5 cases per 1000 person-months). The risk of AIN-2,3 increased with age (odds ratio [OR], 3.09 [95% CI, 1.12-8.52] for men 40-49 years of age and 4.78 [95% CI, 1.29-17.73] for men >50 years of age, compared with men <40 years of age) and for men whose CD4+ cell counts were <50 cells/mm(3) before starting HAART (OR, 14.40 [95% CI, 1.45-143.58]). Men who had been receiving their current HAART regimen for >4 years had a marginally significant lower risk of AIN-2,3 after adjustment for HPV (OR, 0.28 [95% CI, 0.07-1.06]) compared with those treated for <4 years. Anal HPV type 16 (HPV16) or type 18 (HPV18) infections (OR, 14.18; [95% CI, 3.51-57.32]) and HPV16 and HPV18 co-infection (OR, 31.03 [ 95% CI, 5.68-169.60]) were strongly associated with progression to AIN-2,3.
HPV16 and HPV18 infections and a low nadir CD4+ cell count increase the risk of AIN-2,3. Receiving the same HAART regimen for >4 years may contribute some benefit against AIN-2,3.
人类免疫缺陷病毒(HIV)阳性的男男性行为者(MSM)存在发生肛门上皮内瘤变(AIN)和癌症的风险。本研究旨在确定与 HIV 阳性 MSM 的高级别 AIN(AIN-2、3)相关的风险因素,包括接受高效抗逆转录病毒治疗(HAART)。
对 247 名接受 HAART 或开始 HAART 的 HIV 阳性 MSM 进行队列研究,每 6 个月进行一次人乳头瘤病毒(HPV)检测和高分辨率肛门镜检查,以 Cox 回归分析和期间患病率逻辑回归确定 AIN-2、3 的预测因素。
在研究期间,247 名参与者中有 132 名(53%)出现 AIN-2、3。从基线较低异常进展为 AIN-2、3 的进展率为每 1000 人-月 12.8 例(95%置信区间 [CI],每 1000 人-月 9.8-16.5 例)。AIN-2、3 的风险随着年龄的增长而增加(年龄为 40-49 岁的男性,与年龄<40 岁的男性相比,比值比 [OR] 为 3.09 [95%CI,1.12-8.52];年龄>50 岁的男性,OR 为 4.78 [95%CI,1.29-17.73]),并且在开始 HAART 之前 CD4+细胞计数<50 个/mm(3)的男性(OR,14.40 [95%CI,1.45-143.58])。与治疗<4 年的患者相比,当前 HAART 方案治疗>4 年的患者 AIN-2、3 的风险在 HPV 调整后略有降低(OR,0.28 [95%CI,0.07-1.06])。肛门 HPV 型 16(HPV16)或 18(HPV18)感染(OR,14.18;[95%CI,3.51-57.32])和 HPV16 和 HPV18 共同感染(OR,31.03 [95%CI,5.68-169.60])与进展为 AIN-2、3 密切相关。
HPV16 和 HPV18 感染以及最低 CD4+细胞计数会增加 AIN-2、3 的风险。接受相同的 HAART 方案>4 年可能对 AIN-2、3 有一定的预防作用。