Evidence map›Paper›PMID 42821623›Full record

ArticlePLoS neglected tropical diseases2026

Mycobacterium leprae infection, Hansen's disease, and helminth infections: A cross-sectional study in southeastern Brazil.

Audra Bass, Heloine Leite, Lorena B P Oliveira, Emma Nedell, Pedro Marçal, Julie A Clennon, Jeffrey M Collins, Thomas R Ziegler, Erica Magueta Silva, Maisa P Vieira and 6 more

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Article in PLoS neglected tropical 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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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

  • Update of
    2025
5 · Who and what money

Authors and funding

16 authors.

Audra BassDepartment of Medicine, Divisions of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Heloine LeitePrograma of Multicêntrico de Bioquímica e Biologia Molecular/PMBqBM, Universidade Federal de Juiz De Fora-Campus Governador Valadares, Governador Valadares, Minas Gerais, Brazil.
Lorena B P OliveiraDepartment of Health, Universidade Vale do Rio Doce (UNIVALE), Governador Valadares, Minas Gerais, Brazil.
Emma NedellHubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, United States of America.
Pedro MarçalDepartment of Health, Universidade Vale do Rio Doce (UNIVALE), Governador Valadares, Minas Gerais, Brazil.
Julie A ClennonDepartment of Environmental Sciences, Emory University, Atlanta, Georgia, United States of America.
Jeffrey M CollinsDepartment of Medicine, Divisions of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Thomas R ZieglerDepartment of Medicine, Division of Endocrinology, Metabolism and Lipids, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Erica Magueta SilvaPrograma of Multicêntrico de Bioquímica e Biologia Molecular/PMBqBM, Universidade Federal de Juiz De Fora-Campus Governador Valadares, Governador Valadares, Minas Gerais, Brazil.
Maisa P VieiraPrograma of Multicêntrico de Bioquímica e Biologia Molecular/PMBqBM, Universidade Federal de Juiz De Fora-Campus Governador Valadares, Governador Valadares, Minas Gerais, Brazil.
Marcos D S PinheiroPrograma of Multicêntrico de Bioquímica e Biologia Molecular/PMBqBM, Universidade Federal de Juiz De Fora-Campus Governador Valadares, Governador Valadares, Minas Gerais, Brazil.
Alexandre C BrancoCentro de Referência em Doenças Endêmicas e Programas Especiais, Governador Valadares, Minas Gerais, Brazil.
José A FerreiraUnifenas Universidade, Belo Horizonte, Minas Gerais, Brazil.
Lance WallerDepartment of Biostatistics and Bioinformatics, Rollins School of Public health, Emory University, Atlanta, Georgia, United States of America.
Lucia A O FragaPrograma of Multicêntrico de Bioquímica e Biologia Molecular/PMBqBM, Universidade Federal de Juiz De Fora-Campus Governador Valadares, Governador Valadares, Minas Gerais, Brazil.
Jessica K FairleyDepartment of Medicine, Divisions of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0003-4086-9272

Funding

Identifying Risk Factors for Leprosy Transmission Related to Co-infections, Unsafe WASH and Undernutrition Using Novel Serologic Multiplex and High Resolution Metabolomic AssaysR01AI149527 · NIAID · EMORY UNIVERSITY · PI FAIRLEY, JESSICA K. · 2020 to 2023
$624k
NIAID NIH HHS R01 AI149527
6 · The paper itself

Abstract

backgroundNeglected tropical diseases are often co-endemic in affected areas but how they interact is less clear, especially in the case of Hansen's Disease (HD), commonly referred to as leprosy. Prior studies have demonstrated associations between helminths and HD and tuberculosis, but our understanding of the epidemiology of these infections is limited. Our goal was to assess the prevalence and potential associations of Mycobacterium leprae infection and parasitic infections in a sample of community members in a highly endemic area for HD in Minas Gerais, Brazil.

methodsAdults and children ages 3 years and older were enrolled from communities in Governador Valadares, Minas Gerais, Brazil, and nearby municipalities. Questionnaires on demographics and infection history were administered. Serological reactivity against M. leprae, Schistosoma mansoni, and Strongyloides stercoralis was assessed by multiplexed bead assay (MBA). Descriptive, univariate, and multivariate statistics were performed to describe the outcomes and potential associations.

resultsOf 1,311 participants, 72 (5.5%) reported a prior history of HD, 94 (7.2%) tested positive for anti-LID-1, 836 (63.8%) reported having one or more parasitic diseases in the past, 153 (11.7%) tested positive for antibodies to schistosoma egg antigen (SEA), and 69 (5.3%) for antibodies to the Strongyloides stercoralis antigen, NIE. Rural residence and anti-LID-1 showed a positive association (aOR 1.79, CI: 1.07- 3.38) as did rural residence and history of HD (aOR, 1.97, CI: 1.14 - 3.38). While not statistically significant, there was a positive association between anti-LID-1 and NIE antibodies (aOR 1.57, CI: 0.69-3.57), and a negative association between anti-LID-1 and SEA antibodies (aOR 0.79, CI: 0.38 - 1.61).

conclusionWe simultaneously measured seroreactivity among various pathogens. While we did not find that a history of HD and anti-LID-1 positivity were associated with seropositivity to NIE or SEA, our study found a high burden of several neglected tropical diseases (NTDs). There was also a strong association with rural residence and LID-1 positivity warranting investigation into the prevalence and epidemiology of M. leprae infection, as well as potential spatial and environmental risk factors.

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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.