Evidence map›Paper›PMID 41493624›Full record

Observational studyHuman genetics2026

Genetic ancestry proportion influences risk of adverse events from tuberculosis treatment in Brazil.

Jacqueline A Piekos, Gustavo Amorim, Felipe Ridolfi, Marcelo Cordeiro-Santos, Afrânio L Kritski, Marina C Figueiredo, Bruno B Andrade, Adalberto R Santos, David W Haas, Timothy R Sterling and 3 more

Abstract readObservational Study
In one paragraph

Observational study in Human genetics, 2026. 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. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Jacqueline A PiekosVanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA.
Gustavo AmorimDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA.
Felipe RidolfiInstituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Marcelo Cordeiro-SantosFundação Medicina Tropical Dr. Heitor Vieira Dourado, Manaus, Brazil.
Afrânio L KritskiFaculdade de Medicina, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Marina C FigueiredoDivision of Infectious Disease, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Bruno B AndradeMultinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Bahia, Brazil.
Adalberto R SantosLaboratory of Molecular Biology Applied to Mycobacteria, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
David W HaasDivision of Infectious Disease, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Timothy R Sterling *Division of Infectious Disease, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Valeria C Rolla *Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Digna R Velez Edwards *Department of Biomedical Informatics, Vanderbilt University Medical Center, 2525 West End Ave, Suite 1150, Nashville, TN, 37027, USA. digna.r.velez.edwards@vumc.org.
Regional Prospective Observational Research in Tuberculosis (RePORT)-Brazil consortium

Funding

CCASAnet: Caribbean, Central and South America NetworkU01AI069923 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Pedro Enrique Cahn, Jessica L Castilho · 2006 to 2026
$41.6M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Tennessee CFAR: Implementation of Culturally Responsive Trauma-Informed Care with Youth with HIV in Memphis, TNP30AI110527 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John Koethe · 2015 to 2026
$27.5M
Pharmacogenomics of HIV TherapyR01AI077505 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HAAS, DAVID W · 2008 to 2025
$12.3M
Regional Prospective Observational Research in Tuberculosis (RePORT) – Brazil NetworkU01AI172064 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRUNO DE BEZERRIL ANDRADE, TIMOTHY R STERLING · 2023 to 2026
$4.0M
Training Program on Genetic Variation and Human PhenotypesT32GM080178 · NIGMS · VANDERBILT UNIVERSITY · PI COX, NANCY J, SAMUELS, DAVID C · 2007 to 2021
$3.1M
Predictors of treatment toxicity, failure, and relapse in HIV-related tuberculosisR01AI120790 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ROLLA, VALERIA CAVALCANTI, STERLING, TIMOTHY R · 2016 to 2019
$2.6M
NCATS NIH HHS UL1 TR000445NIAID NIH HHS P30 AI110527NIAID NIH HHS R01 AI077505NIAID NIH HHS R01 AI120790NIAID NIH HHS U01 AI069923NIAID NIH HHS U01 AI172064NIGMS NIH HHS T32 GM080178
6 · The paper itself

Abstract

Tuberculosis (TB) treatment is highly effective, but response to therapy varies by geography and population subgroups. We assessed differences in TB treatment response in a representative and heterogeneous Brazilian population. We estimated genetic ancestry according to major genetic ancestry groups (African, European, and Amerindian) in the Regional Prospective Observational Research in Tuberculosis (RePORT)-Brazil cohort using ADMIXTURE software. RePORT-Brazil is an observational prospective cohort study of individuals with newly-diagnosed, culture-confirmed, pulmonary TB. Outcomes attributed to TB treatment included Grade 2 or higher adverse drug reaction (ADR), Grade 3 or higher ADR, hepatic ADR, and failure/recurrence. Genetic ancestry proportions were evaluated as predictors in univariate and multivariable logistic regression models for each outcome, and in stratified models for each genetic ancestry group. There were 930 pulmonary TB patients included in this study. In multivariable models we observed a decreased risk of Grade 2 + ADR when African ancestry proportion increased by 10% (Odds Ratio [OR] 0.41, 95% Confidence Interval [CI] 0.20-0.85) and an increased risk for Grade 2 + ADR with increasing European genetic ancestry (OR 2.33, 95% CI 1.14-4.76). In secondary analyses evaluating the interaction of HIV and genetic ancestry, we observed a statistically significant interaction between HIV and African genetic ancestry, but significantly decreased risk for Grade 2 + ADR with increasing African ancestry proportion. There were no associations with Amerindian genetic ancestry or for other treatment outcomes. In this Brazilian TB cohort, increased toxicity risk was associated with decreased African and increased European ancestry proportion.

Indexed as

Antitubercular AgentsTuberculosisTuberculosis, PulmonaryAdultBlack PeopleBrazilFemaleHumansMaleMiddle AgedProspective StudiesWhite PeopleAntitubercular Agents

Identifiers

PMID41493624
PMCPMC12774987

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.