Evidence map›Paper›PMID 40361016›Full record

Trial reportBMC infectious diseases2025

Tuberculosis disease characteristics associated with mortality, severe morbidity and unsuccessful treatment in people living with HIV treated for tuberculosis - a secondary analysis of the ANRS 12300 Reflate TB2 trial.

Robert Akpata, Jean-Baptiste Ntakpe, Eugène Messou, Nathalie De Castro, Corine Chazallon, Isabel Timana, Rodrigo Escada, Sandra Wagner Cardoso, Nilesh Bhatt, Celso Khosa and 11 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Robert AkpataUniversity of Bordeaux, National Institute for Health and Medical Research (Inserm) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre, 146 Rue Léo Saignat, Bordeaux, 33000, France. robert.akpata@u-bordeaux.fr.
Jean-Baptiste NtakpeUniversity of Bordeaux, National Institute for Health and Medical Research (Inserm) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre, 146 Rue Léo Saignat, Bordeaux, 33000, France.
Eugène MessouProgramme PACCI/ANRS Research Center, Abidjan, Côte d'Ivoire.
Nathalie De CastroUniversity of Bordeaux, National Institute for Health and Medical Research (Inserm) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre, 146 Rue Léo Saignat, Bordeaux, 33000, France.
Corine ChazallonUniversity of Bordeaux, National Institute for Health and Medical Research (Inserm) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre, 146 Rue Léo Saignat, Bordeaux, 33000, France.
Isabel TimanaInstituto Nacional de Saúde, Marracuene, Mozambique.
Rodrigo EscadaNational Institute of Infectious Diseases Evandro Chagas, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Sandra Wagner CardosoNational Institute of Infectious Diseases Evandro Chagas, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Nilesh BhattInstituto Nacional de Saúde, Marracuene, Mozambique.
Celso KhosaInstituto Nacional de Saúde, Marracuene, Mozambique.
Didier LaureillardDepartment of Infectious and Tropical Diseases, Nimes University Hospital, Nimes, France.
Giang Do ChauPham Ngoc Thach Hospital, Ho Chi Minh City, Vietnam.
Frédéric Ello NogbouProgramme PACCI/ANRS Research Center, Abidjan, Côte d'Ivoire.
Donald Diomande GlaoProgramme PACCI/ANRS Research Center, Abidjan, Côte d'Ivoire.
Valdilea VelosoInstituto Nacional de Saúde, Marracuene, Mozambique.
Jean-Michel MolinaInfectious Diseases Department, AP-HP-Hôpital Saint-Louis Lariboisière, Paris, France.
Beatriz GrinsztejnInstituto Nacional de Saúde, Marracuene, Mozambique.
Marcel ZannouUniversité d'Abomey-Calavi, Cotonou, Benin.
Serge EholieProgramme PACCI/ANRS Research Center, Abidjan, Côte d'Ivoire.
Olivier MarcyUniversity of Bordeaux, National Institute for Health and Medical Research (Inserm) UMR 1219, Research Institute for Sustainable Development (IRD) EMR 271, Bordeaux Population Health Centre, 146 Rue Léo Saignat, Bordeaux, 33000, France.
ANRS 12300 Reflate TB2 study Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTuberculosis is a severe disease, not only due to its lethality but also to a significant morbidity occurring in people living with HIV (PLWH). If factors associated to mortality, severe morbidity and unsuccessful treatment related to the host are well identified in PLWH, there is scarce knowledge on factors related to the disease itself such as bacillary load, extent of lung involvement and disease dissemination to other organs. We sought to assess whether tuberculosis-related factors were associated with key patient outcomes in PLWH using data from an international clinical trial.

methodsWe conducted a secondary analysis of the ANRS 12300 Reflate TB2, an international phase III open-label randomized trial that assessed different antiretroviral regimens in PLWH treated for tuberculosis. We evaluated whether bacillary load (smear positivity grade), extent of lung involvement (cavitation on chest x-ray) and disease dissemination (urine LAM positivity) were associated with mortality using Cox proportional hazard models, and to severe morbidity and unsuccessful tuberculosis treatment using logistic regressions.

resultsOf 457 participants included in this study, 90 (20.4%) had grade 2 + or 3 + smear positivity, 39 (10.8%) had cavitation on chest X-ray, and 147 (32.2%) had a positive urinary LAM. Overall, 19 (4.2%) participants died, 113 (24.7%) presented severe morbidity, and 33 (7.2%) had unsuccessful tuberculosis treatment. Factors that remained independently associated with mortality were cavitation on chest x-ray (aHR = 7.92, 95% CI, 1.74-35.94, p = .0073) and LAM positivity (aHR = 5.53, 95% CI, 1.09-28.06, p = .0389). The only factor that remained significantly associated with severe morbidity was LAM positivity (aOR = 2.04, 95% CI, 1.06-3.92, p = .0323). No factor remained significantly associated with unsuccessful tuberculosis treatment.

conclusionsIn PLWH with tuberculosis enrolled in a trial, tuberculosis disease characteristics related to disease severity were cavitation on chest x-ray and urine LAM positivity. Early identification of these factors could help improve the management of PLWH with tuberculosis and improve their survival.

Indexed as

Antitubercular AgentsHIV InfectionsTuberculosisAdultFemaleHumansMaleMiddle AgedTreatment FailureAntitubercular AgentsBacillary loadDisease disseminationExtent of lung involvementHIVMortalitySevere morbidityTuberculosisUnsuccessful treatment

Identifiers

PMID40361016
PMCPMC12077038

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.