Lawson Unit, Department of HIV/Genitourinary Medicine, Brighton and Sussex University Hospitals NHS Trust, Royal Sussex County Hospital, Brighton, UK.
HIV Med. 2011 Oct;12(9):553-61. doi: 10.1111/j.1468-1293.2011.00923.x. Epub 2011 Apr 27.
We compared morbidities in HIV-1-infected patients before and after the introduction of antiretroviral therapy (ART) in a rural Ugandan cohort followed from 1990 to 2008. ART was introduced in 2004.
Random-effects Poisson regression models were used to estimate incidence rates of World Health Organization (WHO) stage-defining diseases in HIV-infected individuals aged 13 years or older with known seroconversion dates, and in an age-stratified sample of HIV-negative individuals.
The most common morbid event was bacterial pneumonia, with an incidence of 7.4/100 person-years (pyr) among 309 HIV seroconverters and 1.3/100 pyr among 348 HIV-negative participants [hazard ratio (HR) 5.64; 95% confidence interval (CI) 3.6-8.8]. Among seroconverters, the incidence of the acquisition of any WHO stage-defining disease rose from 14.4/100 pyr (95% CI 11.1-18.6) in 1990-1998 to 46.0/100 pyr (95% CI 37.7-56.0) in 1999-2003. Following the introduction of ART, the incidence among seroconverters declined to 36.4/100 pyr (95% CI 27.1-48.9) in 2004-2005 and to 28.3/100 pyr (95% CI 21.2-37.8) in 2006-2008. At the individual level, a higher rate of acquiring any WHO stage-defining disease was independently associated with lower CD4 cell count, longer duration of HIV infection and older age. In addition, individuals who had been on ART for longer than 12 months had a substantially lower rate of any WHO stage disease than those not yet on ART (adjusted HR 0.35; 95% CI 0.2-0.6).
Morbidity in HIV-positive participants decreased following the introduction of ART, and this decline was more marked with increasing duration on ART. The benefits of decreased HIV-related morbidity from ART lend support to urgent efforts to ensure universal access to early diagnosis of HIV infection and to ART, especially in rural Africa.
我们比较了在引入抗逆转录病毒疗法(ART)前后感染 HIV-1 的患者的发病率,该研究在一个从 1990 年到 2008 年随访的乌干达农村队列中进行。ART 于 2004 年引入。
使用随机效应泊松回归模型估计已知血清转换日期的年龄在 13 岁或以上的 HIV 感染者和年龄分层的 HIV 阴性个体中世界卫生组织(WHO)定义的疾病的发病率。
最常见的疾病是细菌性肺炎,在 309 名 HIV 血清转换者和 348 名 HIV 阴性参与者中,其发病率为 7.4/100 人年(pyr)[危险比(HR)5.64;95%置信区间(CI)3.6-8.8]。在血清转换者中,任何 WHO 定义的疾病的发病率从 1990-1998 年的 14.4/100 pyr(95%CI 11.1-18.6)上升到 1999-2003 年的 46.0/100 pyr(95%CI 37.7-56.0)。ART 引入后,血清转换者的发病率在 2004-2005 年降至 36.4/100 pyr(95%CI 27.1-48.9),在 2006-2008 年降至 28.3/100 pyr(95%CI 21.2-37.8)。在个体水平上,更高的获得任何 WHO 定义的疾病的比率与较低的 CD4 细胞计数、较长的 HIV 感染时间和较大的年龄独立相关。此外,接受 ART 治疗超过 12 个月的患者获得任何 WHO 疾病的比率明显低于未接受 ART 治疗的患者(调整后的 HR 0.35;95%CI 0.2-0.6)。
ART 引入后,HIV 阳性参与者的发病率下降,而随着 ART 持续时间的延长,发病率下降更为显著。ART 减少与 HIV 相关的发病率的益处支持了紧急努力,以确保早期诊断 HIV 感染和获得 ART 的普遍机会,特别是在非洲农村。