Association between c reactive protein and all-cause mortality in the elsa-brasil cohort

dc.creatorChams Bmaluf
dc.creatorFrancesco p Cappuccio
dc.creatorMichelle a Miller
dc.creatorSandhi Maria Barreto
dc.creatorLuana Giatti
dc.creatorAntonio Luiz Pinho Ribeiro
dc.creatorPedro g Vidigal
dc.creatorDouglas r m Azevedo
dc.creatorRosane h Griep
dc.creatorSheila Maria Alvim Matos
dc.creatorChen ji
dc.date.accessioned2023-10-02T21:38:43Z
dc.date.accessioned2025-09-09T00:43:08Z
dc.date.available2023-10-02T21:38:43Z
dc.date.issued2020-01-22
dc.format.mimetypepdf
dc.identifier.doidoi:10.1136/jech-2019-213289
dc.identifier.issn0143005X
dc.identifier.urihttps://hdl.handle.net/1843/59077
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofJournal of Epidemiology and Community Health
dc.rightsAcesso Aberto
dc.subjectC-Reactive Protein
dc.subjectMortality
dc.subjectCardiovascular Diseases
dc.subject.otherC reactive protein
dc.subject.otherMortality
dc.subject.otherCardiovascular Diseases
dc.titleAssociation between c reactive protein and all-cause mortality in the elsa-brasil cohort
dc.typeArtigo de periódico
local.citation.epage427
local.citation.spage421
local.citation.volume74
local.description.resumoBackground High-sensitivity C reactive protein (hsCRP) has been proposed as a marker of incident cardiovascular disease and vascular mortality, and may also be a marker of non-vascular mortality. However, most evidence comes from either North American or European cohorts. The present proposal aims to investigate the association of hsCRP with the risk of all-cause mortality in a multiethnic Brazilian population. Methods Baseline data (2008–2010) of a cohort of 14 238 subjects participating in the Brazilian Longitudinal Study of Adult Health were used. hsCRP was assayed with immunochemistry. The association of baseline covariates with all-cause mortality was calculated by Cox regression for univariate model and adjusted for different confounders after a mean follow-up of 8.0±1.1 years. The final model was adjusted for age, sex, self-rated race/ethnicity, schooling, health behaviours and prevalent chronic disease.Results The risk of death increased steadily by quartiles of hsCRP, from 1.45 (95% CI 1.05 to 2.01) in quartile 2 to 1.95 (95% CI 1.42 to 2.69) in quartile 4, compared with quartile 1. Furthermore, the persistence of a significant graded association after the exclusion of deaths in the first year of follow-up suggests that these results are unlikely to be due to reverse causality. Finally, the HR was unaffected by the exclusion of participants who had selfreported medical history of diabetes, cancer and chronic obstructive pulmonary disease.Conclusions Our study shows that hsCRP level is associated with mortality in a highly admixed population, independent of a large set of lifestyle and clinical variables.
local.publisher.countryBrasil
local.publisher.departmentMED - DEPARTAMENTO DE CLÍNICA MÉDICA
local.publisher.departmentMED - DEPARTAMENTO DE MEDICINA PREVENTIVA SOCIAL
local.publisher.departmentMED - DEPARTAMENTO DE PROPEDÊUTICA COMPLEMENTAR
local.publisher.initialsUFMG
local.url.externahttps://pubmed.ncbi.nlm.nih.gov/32102838/

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