Blood and urine early treatment response biomarkers in HIV-associated disseminated tuberculosis.

Southern African journal of HIV medicine Pub Date : 2025-04-09 eCollection Date: 2025-01-01 DOI:10.4102/sajhivmed.v26i1.1664
Linda Boloko, Marcia Vermeulen, Bianca Sossen, Abulele Bekiswa, Phiona E Namale, Chad Centner, Robert J Wilkinson, Charlotte Schutz, Graeme Meintjes, David A Barr
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Abstract

Background: Treatment response biomarkers are needed in the care of patients hospitalised with HIV-associated tuberculosis (TB).

Objectives: We describe the changes in bacillary load during early treatment using quantitative and semi-quantitative measures of Mycobacterium tuberculosis in blood and urine.

Method: We collected serial blood and urine samples at multiple timepoints in consenting adult patients with HIV and positive urine lipoarabinomannan (LAM), admitted to Mitchells Plain Hospital, Cape Town. Blood and urine Xpert Ultra, mycobacterial blood culture and urine LAM were performed. Survival analysis and mixed-effects modelling were used to determine time to a negative test, and to give the predicted probability of a positive test at the different timepoints.

Results: Sixteen participants, predominantly male (63%), with median age 39 years (interquartile range [IQR] 36-43), and CD4 count 27 cells/mm3 (IQR 8-83) were included. At day 14, urine LAM, urine Xpert Ultra and blood Xpert Ultra remained positive in between 75% and 86% of the participants. A mixed-effects model predicted a decline in ordinal values of urine Xpert Ultra (cycle threshold), blood Xpert Ultra (cycle threshold) and blood culture (time-to-positivity) in response to anti-TB treatment. Conversely, urine LAM grade intensity increased over the 14 days.

Conclusion: M. tuberculosis DNA was detectable in urine and blood in decreasing quantity up to 14 days of standard treatment in patients with HIV-associated TB. Urine Alere LAM showed an increasing grade intensity during this period. Further research in larger groups and extended periods are needed to assess relation to clinical outcomes.

hiv相关弥散性结核病的血液和尿液早期治疗反应生物标志物
背景:治疗反应生物标志物在hiv相关结核病住院患者的护理中是必需的。目的:我们通过血液和尿液中结核分枝杆菌的定量和半定量测量来描述早期治疗期间细菌负荷的变化。方法:我们在多个时间点收集了开普敦mitchell平原医院的HIV和尿脂阿拉伯糖甘露聚糖(LAM)阳性的成年患者的连续血液和尿液样本。血、尿Xpert Ultra、分枝杆菌血培养、尿LAM检测。使用生存分析和混合效应模型来确定阴性试验的时间,并给出在不同时间点阳性试验的预测概率。结果:16名参与者,主要是男性(63%),中位年龄39岁(四分位数范围[IQR] 36-43), CD4计数27个细胞/mm3 (IQR 8-83)。在第14天,尿液LAM、尿液Xpert Ultra和血液Xpert Ultra在75%到86%的参与者中保持阳性。混合效应模型预测抗结核治疗后尿Xpert Ultra(周期阈值)、血Xpert Ultra(周期阈值)和血培养(阳性时间)的序数值下降。相反,尿液LAM等级强度在14天内增加。结论:hiv相关结核患者在标准治疗后14天尿液和血液中检测到结核分枝杆菌DNA,数量呈下降趋势。尿Alere LAM在此期间表现为分级强度增加。需要在更大的群体和更长的时间内进行进一步的研究来评估与临床结果的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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