Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil

Detalhes bibliográficos
Autor(a) principal: Bensenor, Isabela M.
Data de Publicação: 2022
Outros Autores: Goulart, Alessandra C., Pereira, Alexandre C., Brunoni, André R., Alencar, Airlane, Santos, Raul D., Bittencourt, Márcio S., Telles, Rosa W., Machado, Luciana Andrade Carneiro, Barreto, Sandhi Maria, Almeida-Pititto, Bianca de, Janovsky, Carolina Porto Silva, Sgarbi, José Augusto, Tebar, William R., Meneghini, Vandrize, Barbosa Junior, Fernando, Ribeiro, Ana Cristina de Medeiros, Pasoto, Sandra Gofinet, Pereira, Rosa Maria R., Bonfá, Eloísa, Sipahi, Aytan M., Santos, Itamar de S., Lotufo, Paulo A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/213307
Resumo: Objectives: This analysis describes the protocol of a study with a case-cohort to design to prospectively evaluate the incidence of subclinical atherosclerosis and Cardiovascular Disease (CVD) in Chronic Inflammatory Disease (CID) participants compared to non-diseased ones. Methods: A high-risk group for CID was defined based on data collected in all visits on self-reported medical diagnosis, use of medicines, and levels of high-sensitivity C-Reactive Protein >10 mg/L. The comparison group is the Aleatory Cohort Sample (ACS): a group with 10% of participants selected at baseline who represent the entire cohort. In both groups, specific biomarkers for DIC, markers of subclinical atherosclerosis, and CVD morbimortality will be tested using weighted Cox. Results: The high-risk group (n = 2,949; aged 53.6 ± 9.2; 65.5% women) and the ACS (n=1543; 52.2±8.8; 54.1% women) were identified. Beyond being older and mostly women, participants in the high-risk group present low average income (29.1% vs. 24.8%, p < 0.0001), higher BMI (Kg/m2) (28.1 vs. 26.9, p < 0.0001), higher waist circumference (cm) (93.3 vs. 91, p < 0.0001), higher frequencies of hypertension (40.2% vs. 34.5%, p < 0.0001), diabetes (20.7% vs. 17%, p = 0.003) depression (5.8% vs. 3.9%, p = 0.007) and higher levels of GlycA a new inflammatory marker (p < 0.0001) compared to the ACS. Conclusions: The high-risk group selected mostly women, older, lower-income/education, higher BMI, waist circumference, and of hypertension, diabetes, depression, and higher levels of GlycA when compared to the ACS. The strategy chosen to define the high-risk group seems adequate given that multiple sociodemographic and clinical characteristics are compatible with CID.
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spelling Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-BrasilChronic Inflammatory diseaseCardiovascular diseaseCoronary artery calcium (CAC)arotid intima-media thickness (CIMT)Fatal and non-fatal cardiovascular eventsObjectives: This analysis describes the protocol of a study with a case-cohort to design to prospectively evaluate the incidence of subclinical atherosclerosis and Cardiovascular Disease (CVD) in Chronic Inflammatory Disease (CID) participants compared to non-diseased ones. Methods: A high-risk group for CID was defined based on data collected in all visits on self-reported medical diagnosis, use of medicines, and levels of high-sensitivity C-Reactive Protein >10 mg/L. The comparison group is the Aleatory Cohort Sample (ACS): a group with 10% of participants selected at baseline who represent the entire cohort. In both groups, specific biomarkers for DIC, markers of subclinical atherosclerosis, and CVD morbimortality will be tested using weighted Cox. Results: The high-risk group (n = 2,949; aged 53.6 ± 9.2; 65.5% women) and the ACS (n=1543; 52.2±8.8; 54.1% women) were identified. Beyond being older and mostly women, participants in the high-risk group present low average income (29.1% vs. 24.8%, p < 0.0001), higher BMI (Kg/m2) (28.1 vs. 26.9, p < 0.0001), higher waist circumference (cm) (93.3 vs. 91, p < 0.0001), higher frequencies of hypertension (40.2% vs. 34.5%, p < 0.0001), diabetes (20.7% vs. 17%, p = 0.003) depression (5.8% vs. 3.9%, p = 0.007) and higher levels of GlycA a new inflammatory marker (p < 0.0001) compared to the ACS. Conclusions: The high-risk group selected mostly women, older, lower-income/education, higher BMI, waist circumference, and of hypertension, diabetes, depression, and higher levels of GlycA when compared to the ACS. The strategy chosen to define the high-risk group seems adequate given that multiple sociodemographic and clinical characteristics are compatible with CID.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2022-04-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/21330710.1016/j.clinsp.2022.100013Clinics; v. 77 (2022); 100013Clinics; Vol. 77 (2022); 100013Clinics; Vol. 77 (2022); 1000131980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/213307/195255Copyright (c) 2023 Clinicsinfo:eu-repo/semantics/openAccessBensenor, Isabela M.Goulart, Alessandra C.Pereira, Alexandre C.Brunoni, André R.Alencar, AirlaneSantos, Raul D.Bittencourt, Márcio S.Telles, Rosa W.Machado, Luciana Andrade CarneiroBarreto, Sandhi MariaAlmeida-Pititto, Bianca deJanovsky, Carolina Porto SilvaSgarbi, José AugustoTebar, William R.Meneghini, VandrizeBarbosa Junior, FernandoRibeiro, Ana Cristina de MedeirosPasoto, Sandra GofinetPereira, Rosa Maria R.Bonfá, EloísaSipahi, Aytan M.Santos, Itamar de S.Lotufo, Paulo A.2023-06-18T13:18:36Zoai:revistas.usp.br:article/213307Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2023-06-18T13:18:36Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
title Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
spellingShingle Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
Bensenor, Isabela M.
Chronic Inflammatory disease
Cardiovascular disease
Coronary artery calcium (CAC)
arotid intima-media thickness (CIMT)
Fatal and non-fatal cardiovascular events
title_short Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
title_full Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
title_fullStr Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
title_full_unstemmed Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
title_sort Chronic inflammatory diseases, subclinical atherosclerosis, and cardiovascular diseases: Design, objectives, and baseline characteristics of a prospective case-cohort study ‒ ELSA-Brasil
author Bensenor, Isabela M.
author_facet Bensenor, Isabela M.
Goulart, Alessandra C.
Pereira, Alexandre C.
Brunoni, André R.
Alencar, Airlane
Santos, Raul D.
Bittencourt, Márcio S.
Telles, Rosa W.
Machado, Luciana Andrade Carneiro
Barreto, Sandhi Maria
Almeida-Pititto, Bianca de
Janovsky, Carolina Porto Silva
Sgarbi, José Augusto
Tebar, William R.
Meneghini, Vandrize
Barbosa Junior, Fernando
Ribeiro, Ana Cristina de Medeiros
Pasoto, Sandra Gofinet
Pereira, Rosa Maria R.
Bonfá, Eloísa
Sipahi, Aytan M.
Santos, Itamar de S.
Lotufo, Paulo A.
author_role author
author2 Goulart, Alessandra C.
Pereira, Alexandre C.
Brunoni, André R.
Alencar, Airlane
Santos, Raul D.
Bittencourt, Márcio S.
Telles, Rosa W.
Machado, Luciana Andrade Carneiro
Barreto, Sandhi Maria
Almeida-Pititto, Bianca de
Janovsky, Carolina Porto Silva
Sgarbi, José Augusto
Tebar, William R.
Meneghini, Vandrize
Barbosa Junior, Fernando
Ribeiro, Ana Cristina de Medeiros
Pasoto, Sandra Gofinet
Pereira, Rosa Maria R.
Bonfá, Eloísa
Sipahi, Aytan M.
Santos, Itamar de S.
Lotufo, Paulo A.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Bensenor, Isabela M.
Goulart, Alessandra C.
Pereira, Alexandre C.
Brunoni, André R.
Alencar, Airlane
Santos, Raul D.
Bittencourt, Márcio S.
Telles, Rosa W.
Machado, Luciana Andrade Carneiro
Barreto, Sandhi Maria
Almeida-Pititto, Bianca de
Janovsky, Carolina Porto Silva
Sgarbi, José Augusto
Tebar, William R.
Meneghini, Vandrize
Barbosa Junior, Fernando
Ribeiro, Ana Cristina de Medeiros
Pasoto, Sandra Gofinet
Pereira, Rosa Maria R.
Bonfá, Eloísa
Sipahi, Aytan M.
Santos, Itamar de S.
Lotufo, Paulo A.
dc.subject.por.fl_str_mv Chronic Inflammatory disease
Cardiovascular disease
Coronary artery calcium (CAC)
arotid intima-media thickness (CIMT)
Fatal and non-fatal cardiovascular events
topic Chronic Inflammatory disease
Cardiovascular disease
Coronary artery calcium (CAC)
arotid intima-media thickness (CIMT)
Fatal and non-fatal cardiovascular events
description Objectives: This analysis describes the protocol of a study with a case-cohort to design to prospectively evaluate the incidence of subclinical atherosclerosis and Cardiovascular Disease (CVD) in Chronic Inflammatory Disease (CID) participants compared to non-diseased ones. Methods: A high-risk group for CID was defined based on data collected in all visits on self-reported medical diagnosis, use of medicines, and levels of high-sensitivity C-Reactive Protein >10 mg/L. The comparison group is the Aleatory Cohort Sample (ACS): a group with 10% of participants selected at baseline who represent the entire cohort. In both groups, specific biomarkers for DIC, markers of subclinical atherosclerosis, and CVD morbimortality will be tested using weighted Cox. Results: The high-risk group (n = 2,949; aged 53.6 ± 9.2; 65.5% women) and the ACS (n=1543; 52.2±8.8; 54.1% women) were identified. Beyond being older and mostly women, participants in the high-risk group present low average income (29.1% vs. 24.8%, p < 0.0001), higher BMI (Kg/m2) (28.1 vs. 26.9, p < 0.0001), higher waist circumference (cm) (93.3 vs. 91, p < 0.0001), higher frequencies of hypertension (40.2% vs. 34.5%, p < 0.0001), diabetes (20.7% vs. 17%, p = 0.003) depression (5.8% vs. 3.9%, p = 0.007) and higher levels of GlycA a new inflammatory marker (p < 0.0001) compared to the ACS. Conclusions: The high-risk group selected mostly women, older, lower-income/education, higher BMI, waist circumference, and of hypertension, diabetes, depression, and higher levels of GlycA when compared to the ACS. The strategy chosen to define the high-risk group seems adequate given that multiple sociodemographic and clinical characteristics are compatible with CID.
publishDate 2022
dc.date.none.fl_str_mv 2022-04-06
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/213307
10.1016/j.clinsp.2022.100013
url https://www.revistas.usp.br/clinics/article/view/213307
identifier_str_mv 10.1016/j.clinsp.2022.100013
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/213307/195255
dc.rights.driver.fl_str_mv Copyright (c) 2023 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2023 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; v. 77 (2022); 100013
Clinics; Vol. 77 (2022); 100013
Clinics; Vol. 77 (2022); 100013
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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