Evidence map›Paper›PMID 38867238›Full record

ArticleInternational journal for equity in health2024

Racial inequalities in the development of multimorbidity of chronic conditions: results from a Brazilian prospective cohort.

Fernanda Esthefane Garrides Oliveira, Rosane Härter Griep, Dora Chor, Sandhi Maria Barreto, Maria Del Carmen Bisi Molina, Luciana A C Machado, Maria de Jesus Mendes da Fonseca, Leonardo Soares Bastos

Abstract read
In one paragraph

Article in International journal for equity in health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

8 authors.

Fernanda Esthefane Garrides OliveiraSérgio Arouca National School of Public Health, Oswaldo Cruz Foundation, 4365 Brazil Avenue, Manguinhos, Rio de Janeiro, 21040900, Brazil. fergarrides@gmail.com.
Rosane Härter GriepLaboratory of Health and Environment Education, Oswaldo Cruz Institute, Rio de Janeiro, Brazil.
Dora ChorSérgio Arouca National School of Public Health, Oswaldo Cruz Foundation, 4365 Brazil Avenue, Manguinhos, Rio de Janeiro, 21040900, Brazil.
Sandhi Maria BarretoDepartment of Preventive and Social Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Maria Del Carmen Bisi MolinaFederal University of Espírito Santo, Vitória, Brazil.
Luciana A C MachadoClinical Hospital/EBSERH, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Maria de Jesus Mendes da FonsecaSérgio Arouca National School of Public Health, Oswaldo Cruz Foundation, 4365 Brazil Avenue, Manguinhos, Rio de Janeiro, 21040900, Brazil.
Leonardo Soares BastosScientific Computing Program, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico Productivity ScholarshipFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro PhD grant Nota 10 E-26/200,636/2021Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro Scientist of Our State programFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro Young Scientist of Our State program E-26/201,277/2021
6 · The paper itself

Abstract

backgroundThe occurrence of multimorbidity and its impacts have differentially affected population subgroups. Evidence on its incidence has mainly come from high-income regions, with limited exploration of racial disparities. This study investigated the association between racial groups and the development of multimorbidity and chronic conditions in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil).

methodsData from self-reported white, brown (pardos or mixed-race), and black participants at baseline of ELSA-Brasil (2008-2010) who were at risk for multimorbidity were analysed. The development of chronic conditions was assessed through in-person visits and self-reported diagnosis via telephone until the third follow-up visit (2017-2019). Multimorbidity was defined when, at the follow-up visit, the participant had two or more morbidities. Cumulative incidences, incidence rates, and adjusted incidence rate ratios (IRRs) were estimated using Poisson models.

resultsOver an 8.3-year follow-up, compared to white participants: browns had a 27% greater incidence of hypertension and obesity; and blacks had a 62% and 45% greater incidence, respectively. Blacks also had 58% more diabetes. The cancer incidence was greater among whites. Multimorbidity affected 41% of the participants, with a crude incidence rate of 57.5 cases per 1000 person-years (ranging from 56.3 for whites to 63.9 for blacks). Adjusted estimates showed a 20% higher incidence of multimorbidity in black participants compared to white participants (IRR: 1.20; 95% CI: 1.05-1.38).

conclusionsSignificant racial disparities in the risk of chronic conditions and multimorbidity were observed. Many associations revealed a gradient increase in illness risk according to darker skin tones. Addressing fundamental causes such as racism and racial discrimination, alongside considering social determinants of health, is vital for comprehensive multimorbidity care. Intersectoral, equitable policies are essential for ensuring health rights for historically marginalized groups.

Indexed as

MultimorbidityAdultAgedBlack PeopleBrazilChronic DiseaseFemaleHealth Status DisparitiesHumansIncidenceLongitudinal StudiesMaleMiddle AgedProspective StudiesRacial GroupsSocioeconomic FactorsAgingHealth inequality monitoringHealth inequitiesLongitudinal studiesMultimorbidityNoncommunicable diseasesRacial inequalities in healthRacismSocial determinants of health

Identifiers

PMID38867238
PMCPMC11170781

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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.