Evidence map›Paper›PMID 40759946›Full record

ArticleBMC public health2025

The Minha Casa Minha Vida social housing programme and leprosy in Brazil: an analysis of the 100 Million Brazilian Cohort (2010-2015).

Camila S S Teixeira, Júlia M Pescarini, Mauro N Sanchez, Andrêa Jacqueline F Ferreira, Rosemeire L Fiaccone, Maria Yury Ichihara, Renzo Flores-Ortiz, Elizabeth B Brickley, Peter Craig, Alastair H Leyland and 5 more

Abstract read
In one paragraph

Article in BMC public health, 2025. 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

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

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

15 authors.

Camila S S TeixeiraOswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil. csst.camila@gmail.com.
Júlia M PescariniOswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil.
Mauro N SanchezOswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil.
Andrêa Jacqueline F FerreiraOswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil.
Rosemeire L FiacconeOswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil.
Maria Yury IchiharaOswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil.
Renzo Flores-OrtizOswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil.
Elizabeth B BrickleyFaculty of Epidemiology and Population Health, London School of Hygiene & Tropical Medicine, London, United Kingdom.
Peter CraigInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland.
Alastair H LeylandInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland.
Srinivasa Vittal KatikireddiInstitute of Health & Wellbeing, University of Glasgow, Glasgow, Scotland.
Maria Lucia F PennaDepartment of Epidemiology and Biostatistics, Fluminense Federal University (UFF), Rio de Janeiro, Brazil.
Gerson O Penna *Tropical Medicine Center, University of Brasilia (UnB), Brasília, Brazil.
Rita de Cássia Ribeiro-Silva *Oswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil.
Maurício L Barreto *Oswaldo Cruz Foundation - Gonçalo Moniz Institute, Center for Data and Knowledge Integration for Health (CIDACS), Salvador, Bahia, 41 745 - 715, Brazil. mauricio.barreto@fiocruz.br.

Funding

Chief Scientist Office, Scottish Government Health and Social Care Directorate SPHSU13Conselho Nacional de Pesquisa, Ministério da Saúde, Gates Foundation 401739/2015-5Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) Finance Code 001Medical Research Council MC_UU_12017/13National Institute for Health and Care Research GHRG/16/137/99NHS Research Scotland Senior Clinical Fellowship SCAF/15/02Wellcome TrustWellcome Trust 202912/Z/16/Z
6 · The paper itself

Abstract

backgroundEnsuring housing interventions can contribute to improved living conditions which are strong socioeconomic determinants of leprosy. We estimated the association between the social housing programme Minha Casa Minha Vida (MCMVP) and leprosy new cases.

methodsWe followed families registered in the 100 Million Brazilian Cohort linked with MCMVP receipt and nationwide registries of leprosy between 2010 and 2015. We used Cox regression weighted by stabilized inverse probability of treatment weighting (IPTW) to assess the hazard ratio (HR) for the effect of MCMVP on leprosy. Weights were obtained by propensity score using demographic and socioeconomic covariates at baseline. Sensitivity analyses were done considering potential delays to receiving MCMVP, municipality of residence population size and by controlling by the baseline risk of leprosy among potential recipients.

resultsWe followed up 24,584,768 individuals, of which 618,883 (2.5%) were MCMVP recipients, and detected 8,874 new leprosy cases during the study period. Leprosy incidence was higher among MCMVP recipients (13.32/100,000 pyr; 95%CI = 11.45-15.49) compared to non-recipients (11.72/100,000 pyr; 95%CI = 11.47-11.97). MCMVP recipients had higher leprosy incidence (HR = 1.66; 95%CI = 1.34-2.06), compared to non-recipients. Point estimates were lower when considering a delay of 6 or 12 months to moving into the new household (HR = 1.53; 95%CI = 1.20-1.95 and HR = 1.37; 95%CI = 1.05-1.78, respectively), in small/medium municipalities (≤ 300,000 inhabitants) (HR = 1.95; 95%CI = 1.51-2.52), and higher among individuals who subsequently became MCMVP beneficiaries before receiving the benefit (HR = 2.29; 95%CI = 1.93-2.72).

conclusionsThis study found a higher risk of leprosy associated with MCMVP that may reflect reverse causality. Our findings suggest the programme is, in fact, reaching the most vulnerable individuals, as intended in its objectives. Besides, the higher risk of leprosy among MCMVP beneficiaries even before receiving the benefit observed in sensitivity analysis may reflect residual confounding factors related.

Indexed as

LeprosyPublic HousingAdolescentAdultBrazilCohort StudiesFemaleHumansIncidenceMaleMiddle AgedSocioeconomic FactorsYoung AdultCommunicable diseasesInequalityLeprosySocial housingSocioeconomic factors

Identifiers

PMID40759946
PMCPMC12323007

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LicenceCC BY
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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.