Is Urinary Lipoarabinomannan the Result of Renal Tuberculosis? Assessment of the Renal Histology in an Autopsy Cohort of Ugandan HIV-Infected Adults.

Is Urinary Lipoarabinomannan the Result of Renal Tuberculosis? Assessment of the Renal Histology in an Autopsy Cohort of Ugandan HIV-Infected Adults.
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DOI:
10.1371/journal.pone.0123323
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Manabe YC
Manabe YC
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Cox JA;Lukande RL;Kalungi S;Van Marck E;Van de Vijver K;Kambugu A;Nelson AM;Colebunders R;Manabe YC

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尿阿拉伯糖甘露聚糖脂(LAM),分枝杆菌细胞壁成分的检测,用于诊断结核病(TB)。LAM如何进入尿液尚不清楚。为了研究尿LAM阳性是否是肾结核感染的结果,我们在乌干达住院的HIV感染成人尸检队列中将尿LAM抗原检测结果与肾组织学结果相关联。我们进行了一个完整的尸检,包括肾脏采样,在艾滋病毒感染的成年人,在住院期间死亡后,从最近的亲属获得书面知情同意书。通过死后导尿或通过膀胱穿刺收集死后尿液,并用侧向流测定法(LFA)和ELISA测定法检测LAM。两名病理学家评估了肾脏组织学。我们将LAM测定结果与组织学结果相关联。在尿LAM ELISA和/或LFA阳性的13/36(36%)例患者中,8/13(62%)例患者患有肾结核。其余5例LAM阳性患者为播散性结核,无肾脏受累。在23例LAM阴性患者中,3例为播散性结核,无肾脏受累。其余的LAM阴性患者没有结核感染,主要死于真菌和细菌感染。LAM LFA诊断任何部位结核病的敏感性为81%,特异性为100%,LAM ELISA的敏感性为63%,特异性为100%。54%(7/13)的LAM LFA阳性患者在死亡时未接受抗结核治疗。肾结核感染解释了大多数患者的LAM阳性。无肾脏受累的播散性结核病患者也可诊断为LAM。这表明在少数患者中存在导致尿LAM阳性的其他机制。
The detection of urinary lipoarabinomannan (LAM), a mycobacterial cell wall component, is used to diagnose tuberculosis (TB). How LAM enters the urine is not known. To investigate if urinary LAM-positivity is the result of renal TB infection we correlated the outcomes of urinary LAM-antigen testing to renal histology in an autopsy cohort of hospitalized, Ugandan, HIV-infected adults. We performed a complete autopsy, including renal sampling, in HIV-infected adults that died during hospitalization after written informed consent was obtained from the next of kin. Urine was collected postmortem through post-mortem catheterisation or by bladder puncture and tested for LAM with both a lateral flow assay (LFA) and an ELISA assay. Two pathologists assessed the kidney histology. We correlated the LAM-assay results and the histology findings. Of the 13/36 (36%) patients with a positive urinary LAM ELISA and/or LFA, 8/13 (62%) had renal TB. The remaining 5 LAM-positive patients had disseminated TB without renal involvement. Of the 23 LAM-negative patients, 3 had disseminated TB without renal involvement. The remaining LAM-negative patients had no TB infection and died mostly of fungal and bacterial infections. LAM LFA had a sensitivity of 81% and specificity of 100% to diagnose TB at any location, and the LAM ELISA a sensitivity of 63% and a specificity of 100%. 54% (7/13) LAM LFA-positive patients were not on anti-TB treatment at the time of death. Renal TB infection explained LAM-positivity in the majority of patients. Patients with disseminated TB without renal involvement can also be diagnosed with LAM. This suggests that other mechanisms that lead to urinary LAM-positivity exist in a minority of patients.
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