Affiliations 

  • 1 Kirby Institute, University of New South Wales, Sydney, Australia
  • 2 Hospital J.M. Ramos Mejia, Buenos, Argentina
  • 3 Department of Medicine, University of Malaya, Kuala Lumpur, Malaysia
  • 4 Thai Red Cross AIDS Research Centre, Bangkok, Thailand
  • 5 CART Clinical Research Site, Infectious Diseases Medical Centre, Voluntary Health Services (VHS), Chennai, India
  • 6 JOSHA Research, Bloemfontein, South Africa
  • 7 Perinatal HIV Research Unit, Chris Hani Baragwanath Hospital, Soweto, South Africa
  • 8 Plateau State Specialist Hospital, Bingham University Teaching Hospital, Jos, Nigeria; and
  • 9 Desmond Tutu HIV Centre, Institute of Infectious Diseases and Molecular Medicine, University of Cape Town, Cape Town, South Africa
J Acquir Immune Defic Syndr, 2021 May 01;87(1):720-729.
PMID: 33399309 DOI: 10.1097/QAI.0000000000002619

Abstract

BACKGROUND: Tuberculosis (TB) is a common infection in people living with HIV. However, the risk factors for HIV/TB co-infection in second-line HIV therapy are poorly understood. We aimed to determine the incidence and risk factors for TB co-infection in SECOND-LINE, an international randomized clinical trial of second-line HIV therapy.

METHODS: We did a cohort analysis of TB cases in SECOND-LINE. TB cases included any clinical or laboratory-confirmed diagnoses and/or commencement of treatment for TB after randomization. Baseline factors associated with TB were analyzed using Cox regression stratified by site.

RESULTS: TB cases occurred at sites in Argentina, India, Malaysia, Nigeria, South Africa, and Thailand, in a cohort of 355 of the 541 SECOND-LINE participants. Overall, 20 cases of TB occurred, an incidence rate of 3.4 per 100 person-years (95% CI: 2.1 to 5.1). Increased TB risk was associated with a low CD4+-cell count (≤200 cells/μL), high viral load (>200 copies/mL), low platelet count (<150 ×109/L), and low total serum cholesterol (≤4.5 mmol/L) at baseline. An increased risk of death was associated with TB, adjusted for CD4, platelets, and cholesterol. A low CD4+-cell count was significantly associated with incident TB, mortality, other AIDS diagnoses, and virologic failure.

DISCUSSION: The risk of TB remains elevated in PLHIV in the setting of second-line HIV therapy in TB endemic regions. TB was associated with a greater risk of death. Finding that low CD4+ T-cell count was significantly associated with poor outcomes in this population supports the value of CD4+ monitoring in HIV clinical management.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.