The Desmond Tutu HIV Centre, Institute for Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa, and Clinical Research Unit, Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
AIDS. 2009 Sep 10;23(14):1875-80. doi: 10.1097/qad.0b013e32832e05c8.
To assess the utility of urine lipoarabinomannan (LAM) detection as a diagnostic screening test for tuberculosis (TB) in HIV-infected patients with advanced immuno deficiency and high prevalence of sputum smear-negative pulmonary disease.
Cross-sectional survey.
Unselected adults enrolling for antiretroviral therapy (ART) in a South African clinic were screened for TB with two sputum samples for fluorescence microscopy and mycobacterial liquid culture. LAM was measured in urine samples using a commercially available enzyme-linked immunosorbent assay.
Sputum culture-positive TB was diagnosed in 58 patients (median CD4 cell count=78 cells/microliter) out of 235 patients screened (TB prevalence=0.25). Cultures were identified as positive after a mean of 24 days (SD=9 days). The sensitivity of sputum microscopy was just 0.14 (specificity=1.00), whereas that of LAM in concentrated urine was 0.38 (P<0.01; specificity=1.00). In those with CD4 cell counts of less than 50, 50-100 and more than 150 cells/microliter, the LAM assay sensitivities were 0.67, 0.41 and 0.13, respectively. Corresponding values for the combined use of the LAM assay and microscopy were 0.67, 0.53 and 0.21, respectively. Among TB patients, detectable LAM was very strongly associated with low CD4 cell counts and advanced clinical stage. All patients who developed TB immune reconstitution disease (n=5) had detectable urinary LAM at baseline.
The LAM assay has substantially superior sensitivity to sputum microscopy as a routine diagnostic TB screening test among patients with CD4 cell counts less than 100 cells/microliter. In one half of such patients, this assay could reduce the mean time to diagnosis by approximately 3 weeks. Furthermore, detectable urinary LAM may predict the development of TB immune reconstitution disease.
评估尿液脂阿拉伯甘露聚糖(LAM)检测作为诊断筛选试验在艾滋病毒感染、免疫功能严重受损和高比例痰涂片阴性肺部疾病的患者中的应用。
横断面调查。
在南非的一家诊所,对接受抗逆转录病毒治疗(ART)的成人进行了筛查,筛查方法是采集两份痰标本进行荧光显微镜检查和分枝杆菌液体培养。使用商业上可用的酶联免疫吸附试验(ELISA)检测尿液中的 LAM。
235 名筛查患者中,有 58 名(中位 CD4 细胞计数=78 个/微升)诊断为痰培养阳性结核病(TB)(TB 患病率=0.25)。培养物在平均 24 天后(SD=9 天)被鉴定为阳性。痰显微镜检查的敏感性仅为 0.14(特异性=1.00),而浓缩尿液中的 LAM 为 0.38(P<0.01;特异性=1.00)。在 CD4 细胞计数<50、50-100 和>150 个/微升的患者中,LAM 检测的敏感性分别为 0.67、0.41 和 0.13。联合使用 LAM 检测和显微镜检查的相应值分别为 0.67、0.53 和 0.21。在结核病患者中,可检测到的 LAM 与低 CD4 细胞计数和晚期临床分期密切相关。所有发生结核病免疫重建疾病(n=5)的患者在基线时均检测到可检测到的尿 LAM。
与痰显微镜检查相比,LAM 检测作为 CD4 细胞计数<100 个/微升患者的常规诊断性结核病筛查试验具有显著更高的敏感性。在一半的此类患者中,该检测可将诊断中位时间缩短约 3 周。此外,可检测到的尿 LAM 可能预测结核病免疫重建疾病的发生。