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Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort
BACKGROUND: 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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307658/ https://www.ncbi.nlm.nih.gov/pubmed/32102838 http://dx.doi.org/10.1136/jech-2019-213289 |
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author | Maluf, Chams B Barreto, Sandhi Maria Giatti, Luana Ribeiro, Antonio Luiz Vidigal, Pedro G Azevedo, Douglas R M Griep, Rosane H Matos, Sheila Maria Alvim Ji, Chen Cappuccio, Francesco P Miller, Michelle A |
author_facet | Maluf, Chams B Barreto, Sandhi Maria Giatti, Luana Ribeiro, Antonio Luiz Vidigal, Pedro G Azevedo, Douglas R M Griep, Rosane H Matos, Sheila Maria Alvim Ji, Chen Cappuccio, Francesco P Miller, Michelle A |
author_sort | Maluf, Chams B |
collection | PubMed |
description | BACKGROUND: 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 self-reported 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. |
format | Online Article Text |
id | pubmed-7307658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-73076582020-06-23 Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort Maluf, Chams B Barreto, Sandhi Maria Giatti, Luana Ribeiro, Antonio Luiz Vidigal, Pedro G Azevedo, Douglas R M Griep, Rosane H Matos, Sheila Maria Alvim Ji, Chen Cappuccio, Francesco P Miller, Michelle A J Epidemiol Community Health Original Research BACKGROUND: 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 self-reported 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. BMJ Publishing Group 2020-05 2020-05-01 /pmc/articles/PMC7307658/ /pubmed/32102838 http://dx.doi.org/10.1136/jech-2019-213289 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Original Research Maluf, Chams B Barreto, Sandhi Maria Giatti, Luana Ribeiro, Antonio Luiz Vidigal, Pedro G Azevedo, Douglas R M Griep, Rosane H Matos, Sheila Maria Alvim Ji, Chen Cappuccio, Francesco P Miller, Michelle A Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort |
title | Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort |
title_full | Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort |
title_fullStr | Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort |
title_full_unstemmed | Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort |
title_short | Association between C reactive protein and all-cause mortality in the ELSA-Brasil cohort |
title_sort | association between c reactive protein and all-cause mortality in the elsa-brasil cohort |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7307658/ https://www.ncbi.nlm.nih.gov/pubmed/32102838 http://dx.doi.org/10.1136/jech-2019-213289 |
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