Bock Peter, Jennings Karen, Vermaak Redwaan, Cox Helen, Meintjes Graeme, Fatti Geoffrey, Kruger James, De Azevedo Virginia, Maschilla Leonard, Louis Francoise, Gunst Colette, Grobbelaar Nelis, Dunbar Rory, Limbada Mohammed, Floyd Sian, Grimwood Ashraf, Ayles Helen, Hayes Richard, Fidler Sarah, Beyers Nulda
Desmond Tutu TB Centre, Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Stellenbosch, South Africa.
City of Cape Town Health Services, Cape Town, South Africa.
J Acquir Immune Defic Syndr. 2018 Jan 1;77(1):93-101. doi: 10.1097/QAI.0000000000001560.
Antiretroviral treatment (ART) guidelines recommend life-long ART for all HIV-positive individuals. This study evaluated tuberculosis (TB) incidence on ART in a cohort of HIV-positive individuals starting ART regardless of CD4 count in a programmatic setting at 3 clinics included in the HPTN 071 (PopART) trial in South Africa.
A retrospective cohort analysis of HIV-positive individuals aged ≥18 years starting ART, between January 2014 and November 2015, was conducted. Follow-up was continued until 30 May 2016 or censored on the date of (1) incident TB, (2) loss to follow-up from HIV care or death, or (3) elective transfer out; whichever occurred first.
The study included 2423 individuals. Median baseline CD4 count was 328 cells/μL (interquartile range 195-468); TB incidence rate was 4.41/100 person-years (95% confidence interval [CI]: 3.62 to 5.39). The adjusted hazard ratio of incident TB was 0.27 (95% CI: 0.12 to 0.62) when comparing individuals with baseline CD4 >500 and ≤500 cells/μL. Among individuals with baseline CD4 count >500 cells/μL, there were no incident TB cases in the first 3 months of follow-up. Adjusted hazard of incident TB was also higher among men (adjusted hazard ratio 2.16; 95% CI: 1.41 to 3.30).
TB incidence after ART initiation was significantly lower among individuals starting ART at CD4 counts above 500 cells/μL. Scale-up of ART, regardless of CD4 count, has the potential to significantly reduce TB incidence among HIV-positive individuals. However, this needs to be combined with strengthening of other TB prevention strategies that target both HIV-positive and HIV-negative individuals.
抗逆转录病毒治疗(ART)指南建议所有HIV阳性个体终身接受ART治疗。本研究在南非HPTN 071(PopART)试验中的3家诊所的项目环境中,评估了一组开始接受ART治疗的HIV阳性个体(无论CD4计数如何)的结核病(TB)发病率。
对2014年1月至2015年11月开始接受ART治疗的年龄≥18岁的HIV阳性个体进行回顾性队列分析。随访持续至2016年5月30日,或在以下日期进行截尾:(1)发生TB,(2)失访于HIV治疗或死亡,或(3)选择性转出;以先发生者为准。
该研究纳入了2423名个体。基线CD4计数中位数为328个细胞/μL(四分位间距195 - 468);TB发病率为4.41/100人年(95%置信区间[CI]:3.62至5.39)。比较基线CD4>500和≤500个细胞/μL的个体时,发生TB的调整后风险比为0.27(95%CI:0.12至0.62)。在基线CD4计数>500个细胞/μL的个体中,随访的前3个月内无TB发病病例。男性发生TB的调整后风险也更高(调整后风险比2.16;95%CI:1.41至3.30)。
CD4计数高于500个细胞/μL开始接受ART治疗的个体,开始ART治疗后的TB发病率显著较低。无论CD4计数如何,扩大ART治疗有可能显著降低HIV阳性个体中的TB发病率。然而,这需要与加强针对HIV阳性和HIV阴性个体的其他TB预防策略相结合。