Geisel School of Medicine at Dartmouth, Lebanon, NH 03756, USA.
Clin Infect Dis. 2013 Jan;56(1):151-8. doi: 10.1093/cid/cis798. Epub 2012 Sep 12.
Active tuberculosis is common among human immunodeficiency virus (HIV)-infected persons living in tuberculosis-endemic areas, but the hazard of subsequent tuberculosis disease has not been quantified in a single prospective cohort.
Among HIV-infected, BCG-immunized adults with CD4 counts ≥200 cells/μL who received placebo in the DarDar tuberculosis vaccine trial in Tanzania, we compared the prospective risk of active tuberculosis between subjects who did and who did not report prior active tuberculosis. All subjects with a positive tuberculin skin test without prior active tuberculosis were offered isoniazid preventive treatment. Definite or probable tuberculosis was diagnosed during active follow-up using rigorous published criteria.
We diagnosed 52 cases of definite and 92 cases of definite/probable tuberculosis among 979 subjects during a median follow-up of 3.2 years. Among the 80 subjects who reported prior active tuberculosis, 11 (13.8%) subsequently developed definite tuberculosis and 17 (21.3%) developed definite/probable tuberculosis, compared with 41 (4.6%) and 75 (8.3%), respectively, of 899 subjects without prior active tuberculosis (definite tuberculosis risk ratio [RR], 3.01; 95% confidence interval [CI], 1.61-5.63, P < .001; definite/probable tuberculosis RR, 2.55; 95% CI, 1.59-4.09, P < .001). In a Cox regression model adjusting for age, CD4 count, and isoniazid receipt, subjects with prior active tuberculosis had substantially greater hazard of subsequent definite tuberculosis (hazard radio [HR], 3.69; 95% CI, 1.79-7.63, P < .001) and definite/probable tuberculosis (HR, 2.78; 95% CI, 1.58-4.87, P < .001).
Compared to subjects without prior tuberculosis, the hazard of active tuberculosis is increased 3-fold among HIV-infected adults with prior active tuberculosis. Clinical Trials Registration. NCT0052195.
在结核病流行地区,人类免疫缺陷病毒(HIV)感染者中活动性结核病很常见,但尚未在单一前瞻性队列中对随后发生结核病的危险进行量化。
在坦桑尼亚进行的达达尔结核病疫苗试验中,我们对 CD4 计数≥200 个/μL 的接受过卡介苗免疫的 HIV 感染成人进行了安慰剂对照,比较了有和无既往活动性结核病报告的受试者中前瞻性活动性结核病的风险。所有结核菌素皮肤试验阳性而无既往活动性结核病的受试者均接受异烟肼预防治疗。使用严格的已发表标准在主动随访期间诊断确诊或可能的结核病。
在中位随访 3.2 年期间,我们在 979 例受试者中诊断了 52 例确诊结核病和 92 例确诊/可能结核病。在 80 例报告有既往活动性结核病的受试者中,11 例(13.8%)随后发生确诊结核病,17 例(21.3%)发生确诊/可能结核病,而 899 例无既往活动性结核病的受试者中分别为 41 例(4.6%)和 75 例(8.3%)(确诊结核病风险比[RR],3.01;95%置信区间[CI],1.61-5.63,P<.001;确诊/可能结核病 RR,2.55;95%CI,1.59-4.09,P<.001)。在校正年龄、CD4 计数和异烟肼治疗后,在 Cox 回归模型中,既往有活动性结核病的受试者发生后续确诊结核病的危险明显更高(危险比[HR],3.69;95%CI,1.79-7.63,P<.001)和确诊/可能结核病(HR,2.78;95%CI,1.58-4.87,P<.001)。
与无既往结核病的受试者相比,既往有活动性结核病的 HIV 感染者发生活动性结核病的危险增加 3 倍。临床试验注册。NCT0052195。