Evidence map›Paper›PMID 42062935›Full record

ArticleBMC infectious diseases2026

Socio-ecological vulnerability subgroups predict adherence and treatment outcomes in multidrug-resistant tuberculosis and HIV: a latent class analysis.

Kevin J Guzman, Allison Wolf, Rubeshan Perumal, Xuan Lu, Resha Boodhram, Boitumelo Seepamore, Karl Reis, K Rivet Amico, Gerald Friedland, Jennifer R Zelnick and 5 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Kevin J GuzmanDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, Suite E101 8th Floor, PH Building 622 W. 168th Street, New York City, NY, 10032, USA.
Allison WolfDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, Suite E101 8th Floor, PH Building 622 W. 168th Street, New York City, NY, 10032, USA.
Rubeshan PerumalCentre for the AIDS Programme of Research in South Africa (CAPRISA), South African Medical Research Council (SAMRC)-CAPRISA-TB-HIV Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal, Durban, South Africa.
Xuan LuDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, Suite E101 8th Floor, PH Building 622 W. 168th Street, New York City, NY, 10032, USA.
Resha BoodhramCentre for the AIDS Programme of Research in South Africa (CAPRISA), South African Medical Research Council (SAMRC)-CAPRISA-TB-HIV Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal, Durban, South Africa.
Boitumelo SeepamoreCentre for the AIDS Programme of Research in South Africa (CAPRISA), South African Medical Research Council (SAMRC)-CAPRISA-TB-HIV Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal, Durban, South Africa.
Karl ReisDepartment of Medicine, University of Washington, Seattle, WA, USA.
K Rivet AmicoUniversity of Michigan School of Public Health, Ann Arbor, MI, USA.
Gerald FriedlandDepartment of Medicine, Division of Infectious Disease, Yale University School of Medicine, New Haven, CT, USA.
Jennifer R ZelnickGraduate School of Social Work, Touro University, New York City, NY, USA.
Amrita DaftaryCentre for the AIDS Programme of Research in South Africa (CAPRISA), South African Medical Research Council (SAMRC)-CAPRISA-TB-HIV Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal, Durban, South Africa.
Matthew CummingsDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, Suite E101 8th Floor, PH Building 622 W. 168th Street, New York City, NY, 10032, USA.
Nesri PadayatchiCentre for the AIDS Programme of Research in South Africa (CAPRISA), South African Medical Research Council (SAMRC)-CAPRISA-TB-HIV Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal, Durban, South Africa.
Kogieleum NaidooCentre for the AIDS Programme of Research in South Africa (CAPRISA), South African Medical Research Council (SAMRC)-CAPRISA-TB-HIV Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal, Durban, South Africa.
Max O'DonnellDivision of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, Suite E101 8th Floor, PH Building 622 W. 168th Street, New York City, NY, 10032, USA. mo2130@cumc.columbia.edu.

Funding

American Thoracic Society PG014635-01Burroughs Wellcome Fund PG014684Charles H. Revson Foundation PG014684National Institute of Allergy and Infectious Diseases 1L60A1194399National Institute of Allergy and Infectious Diseases R01AI124413Stony Wold-Herbert Fund PT24-4036
6 · The paper itself

Abstract

backgroundDespite the availability of effective all-oral regimens, treatment outcomes for rifampicin-resistant or multidrug-resistant tuberculosis (RR/MDR-TB) remain suboptimal, particularly in high HIV-burden settings. Factors across the socio-ecological spectrum strongly influence medication adherence and outcomes, yet approaches to identifying high-risk groups remain limited. We aim to identify clinically meaningful subgroups of individuals with RR/MDR-TB and HIV based on baseline socio-ecological vulnerabilities and examine whether subgroup membership is predictive of medication adherence and treatment outcomes.

methodsEligible participants were adults with confirmed RR/MDR-TB and HIV, initiating a bedaquiline-containing regimen and on antiretroviral therapy (ART), who were prospectively enrolled as part of the PRAXIS study (November 2016 to April 2020) in KwaZulu-Natal, South Africa. Adherence to bedaquiline and ART was measured using a cellular-enabled electronic dose monitor (EDM). We used a latent class analysis (LCA), a method for grouping individuals based on shared characteristics, to identify classes based on shared socio-ecological characteristics. A random forest model was developed and internally validated to predict class assignment. Cox proportional hazard models examined the association between class membership and treatment outcomes.

resultsAmong 370 participants (median age, 36 years, 54% female), LCA identified three distinct socio-ecological classes. Class 1, characterized by severe socio-economic vulnerability, had the lowest treatment success rate (67%), while Class 3, characterized by relative socio-economic stability, had the highest (86%). The random forest model using only four socio-ecological variables achieves 91.9% classification accuracy, with marital status, gender, BMI, and functional status as the strongest predictors of class membership. Adjusted analysis demonstrated class membership independently predicted outcomes, even after accounting for bedaquiline adherence, indicating that structural vulnerabilities confer risk beyond adherence alone.

conclusionIn this study, socio-ecological classes were associated with significantly different treatment outcomes, independent of bedaquiline adherence. Structural vulnerability independently predicted poor outcomes in RR/MDR-TB and HIV, supporting integration of socio-ecological risk stratification into differentiated care models. CLINICAL TRIAL: Not applicable. In a prospective study, we identified socio-ecological subgroups among individuals with RR/MDR-TB and HIV that predict treatment outcomes independent of medication adherence, highlighting the potential of predictive modeling to inform risk stratification and guide patient-centered interventions.

Indexed as

Antitubercular AgentsHIV InfectionsMedication AdherenceTuberculosis, Multidrug-ResistantAdultAnti-HIV AgentsDiarylquinolinesFemaleHumansLatent Class AnalysisMaleProspective StudiesSouth AfricaTreatment Effect HeterogeneityTreatment OutcomeAnti-HIV AgentsAntitubercular AgentsbedaquilineDiarylquinolinesBedaquilineHIVLatent class analysisMedication adherenceRR/MDR-TB

Identifiers

PMID42062935
PMCPMC13277064

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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.