Drain Paul K, Gounder Lilishia, Grobler Anneke, Sahid Faieza, Bassett Ingrid V, Moosa Mahomed-Yunus S
Medical Practice Evaluation Center, Boston, Massachusetts, USA Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Department of Virology, National Health Laboratory Service, Inkosi Albert Luthuli Central Hospital, Durban, South Africa.
BMJ Open. 2015 Apr 15;5(4):e006833. doi: 10.1136/bmjopen-2014-006833.
To determine if urinary lipoarabinomannan (LAM) may serve as a biomarker to monitor antituberculosis (TB) therapy response, and whether LAM results before and after treatment are predictive of patient outcomes.
Prospective cohort.
Outpatient referral clinic and tertiary hospital in South Africa.
Adults (≥18 years) with ≥2 TB-related symptoms (cough, fever, weight loss, night sweats) for ≥2 weeks being initiated on anti-TB therapy.
On enrolment, we obtained urine and nebulised sputum specimens, offered HIV testing and started participants on anti-TB therapy for ≥6 months. We collected urine samples after the 2-month intensive treatment phase and at the completion of anti-TB therapy. Positive LAM results were graded from 1 (low) to 5 (high). Participants were followed for >3 years.
The primary outcome was change in urine LAM results during anti-TB therapy. The secondary outcome was all-cause mortality.
Among 90 participants, 57 (63%) had culture-confirmed pulmonary TB. Among the 88 participants tested, 82 (93%) were HIV-infected with median CD4 168/mm(3) (IQR 89-256/mm(3)). During anti-TB therapy, the percentage of LAM-positive participants decreased from baseline to 2 months (32% to 16%), and from baseline to 6-months (32% to 10%) (p values <0.005). In multivariate longitudinal analyses, urine LAM positivity and grade decreased among those with culture-confirmed pulmonary TB (p<0.0001), and had no change in sputum culture-negative participants. At the 2-month visit, participants with positive laboratory-based LAM or rapid LAM with ≥2+ grade had a significantly greater risk of mortality. In analyses adjusted for age, sex, baseline Karnofsky score and HIV status, participants with a rapid LAM ≥2+ grade after 2 months of anti-TB therapy had a 5.6-fold (95% CI 1.2 to 25.2) greater risk of mortality.
Rapid urine LAM testing may be a valuable tool to monitor anti-TB therapy response and to assess prognosis of patients being treated for pulmonary TB in HIV-endemic regions.
确定尿脂阿拉伯甘露聚糖(LAM)是否可作为监测抗结核(TB)治疗反应的生物标志物,以及治疗前后的LAM检测结果是否能预测患者的预后。
前瞻性队列研究。
南非的门诊转诊诊所和三级医院。
年龄≥18岁、有≥2种与TB相关症状(咳嗽、发热、体重减轻、盗汗)且持续≥2周并开始接受抗结核治疗的成年人。
入组时,我们采集尿液和雾化痰液样本,提供HIV检测,并让参与者开始接受≥6个月的抗结核治疗。在2个月强化治疗阶段结束后及抗结核治疗结束时收集尿液样本。LAM检测结果阳性的分为1级(低)至5级(高)。对参与者进行了超过3年的随访。
主要观察指标是抗结核治疗期间尿LAM检测结果的变化。次要观察指标是全因死亡率。
90名参与者中,57名(63%)经培养确诊为肺结核。在接受检测的88名参与者中,82名(93%)感染了HIV,CD4中位数为168/mm³(四分位间距89 - 256/mm³)。在抗结核治疗期间,LAM检测结果阳性的参与者比例从基线到2个月时从32%降至16%,从基线到6个月时从32%降至10%(p值<0.005)。在多变量纵向分析中,经培养确诊为肺结核的患者尿LAM阳性率和分级下降(p<0.0001),而痰培养阴性的参与者无变化。在2个月的随访时,基于实验室检测的LAM阳性或快速LAM检测结果≥2+级的参与者死亡风险显著更高。在对年龄、性别、基线卡诺夫斯基评分和HIV状态进行校正的分析中,抗结核治疗2个月后快速LAM检测结果≥2+级的参与者死亡风险高5.6倍(95%可信区间1.2至25.2)。
快速尿LAM检测可能是监测抗结核治疗反应及评估HIV流行地区肺结核患者预后的一项有价值的工具。