Urine lipoarabinomannan to monitor antituberculosis therapy response and predict mortality in an HIV-endemic region: a prospective cohort study

• Published in: BMJ open 2015-04, Vol.5 (4), p.e006833-e006833
• Main Authors: Drain, Paul K, Gounder, Lilishia, Grobler, Anneke, Sahid, Faieza, Bassett, Ingrid V, Moosa, Mahomed-Yunus S
• Format: Article
• Language: English
• Subjects: Acquired immune deficiency syndrome; Adult; AIDS; Antitubercular Agents - therapeutic use; Biomarkers - urine; CD4 Lymphocyte Count; Endemic Diseases; Female; HIV; HIV Infections - complications; HIV Infections - epidemiology; HIV/AIDS; Humans; Laboratories; Lipopolysaccharides - urine; Longitudinal Studies; Male; Mass Screening; Middle Aged; Monitoring, Physiologic - methods; Mortality; Multivariate Analysis; Mycobacterium tuberculosis; Patient Outcome Assessment; Prospective Studies; South Africa - epidemiology; Sputum; Tuberculosis; Tuberculosis, Pulmonary - complications; Tuberculosis, Pulmonary - drug therapy; Tuberculosis, Pulmonary - mortality; Tuberculosis, Pulmonary - urine
• ISSN: 2044-6055; 2044-6055
• DOI: 10.1136/bmjopen-2014-006833

Objective 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. Design Prospective cohort. Setting Outpatient referral clinic and tertiary hospital in South Africa. Participants Adults (≥18 years) with ≥2 TB-related symptoms (cough, fever, weight loss, night sweats) for ≥2 weeks being initiated on anti-TB therapy. Interventions 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. Outcome measures The primary outcome was change in urine LAM results during anti-TB therapy. The secondary outcome was all-cause mortality. Results Among 90 participants, 57 (63%) had culture-confirmed pulmonary TB. Among the 88 participants tested, 82 (93%) were HIV-infected with median CD4 168/mm3 (IQR 89–256/mm3). 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