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Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study

Inflammatory markers have been associated with increased risk of cardiovascular mortality in general populations. We assessed whether these associations differ by diabetes status. From a population-based cohort study (n = 62,237) we included all participants with diabetes (n = 1753) and a control gr...

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Autores principales: Løfblad, Lena, Hov, Gunhild Garmo, Åsberg, Arne, Videm, Vibeke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329190/
https://www.ncbi.nlm.nih.gov/pubmed/34341370
http://dx.doi.org/10.1038/s41598-021-94995-8
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author Løfblad, Lena
Hov, Gunhild Garmo
Åsberg, Arne
Videm, Vibeke
author_facet Løfblad, Lena
Hov, Gunhild Garmo
Åsberg, Arne
Videm, Vibeke
author_sort Løfblad, Lena
collection PubMed
description Inflammatory markers have been associated with increased risk of cardiovascular mortality in general populations. We assessed whether these associations differ by diabetes status. From a population-based cohort study (n = 62,237) we included all participants with diabetes (n = 1753) and a control group without diabetes (n = 1818). Cox regression models were used to estimate hazard ratios (HRs) with 95% confidence intervals (CI) for possible associations with cardiovascular mortality of 4 different inflammatory markers; C-reactive protein (CRP), calprotectin, neopterin and lactoferrin. During a median follow-up of 13.9 years, 728 (20.4%) died from cardiovascular disease (CVD). After adjustment for age, sex and diabetes, the associations of all inflammatory markers with risk of cardiovascular mortality were log-linear (all P ≤ 0.017 for trend) and did not differ according to diabetes status (all P ≥ 0.53 for interaction). After further adjustments for established risk factors, only CRP remained independently associated with cardiovascular mortality. HRs were 1.22 (1.12–1.32) per standard deviation higher log(e) CRP concentration and 1.91 (1.50–2.43) when comparing individuals in the top versus bottom quartile. The associations of CRP, calprotectin, lactoferrin and neopterin with cardiovascular mortality did not differ by diabetes, suggesting that any potential prognostic value of these markers is independent of diabetes status.
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spelling pubmed-83291902021-08-04 Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study Løfblad, Lena Hov, Gunhild Garmo Åsberg, Arne Videm, Vibeke Sci Rep Article Inflammatory markers have been associated with increased risk of cardiovascular mortality in general populations. We assessed whether these associations differ by diabetes status. From a population-based cohort study (n = 62,237) we included all participants with diabetes (n = 1753) and a control group without diabetes (n = 1818). Cox regression models were used to estimate hazard ratios (HRs) with 95% confidence intervals (CI) for possible associations with cardiovascular mortality of 4 different inflammatory markers; C-reactive protein (CRP), calprotectin, neopterin and lactoferrin. During a median follow-up of 13.9 years, 728 (20.4%) died from cardiovascular disease (CVD). After adjustment for age, sex and diabetes, the associations of all inflammatory markers with risk of cardiovascular mortality were log-linear (all P ≤ 0.017 for trend) and did not differ according to diabetes status (all P ≥ 0.53 for interaction). After further adjustments for established risk factors, only CRP remained independently associated with cardiovascular mortality. HRs were 1.22 (1.12–1.32) per standard deviation higher log(e) CRP concentration and 1.91 (1.50–2.43) when comparing individuals in the top versus bottom quartile. The associations of CRP, calprotectin, lactoferrin and neopterin with cardiovascular mortality did not differ by diabetes, suggesting that any potential prognostic value of these markers is independent of diabetes status. Nature Publishing Group UK 2021-08-02 /pmc/articles/PMC8329190/ /pubmed/34341370 http://dx.doi.org/10.1038/s41598-021-94995-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Løfblad, Lena
Hov, Gunhild Garmo
Åsberg, Arne
Videm, Vibeke
Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study
title Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study
title_full Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study
title_fullStr Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study
title_full_unstemmed Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study
title_short Inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the HUNT study
title_sort inflammatory markers and risk of cardiovascular mortality in relation to diabetes status in the hunt study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8329190/
https://www.ncbi.nlm.nih.gov/pubmed/34341370
http://dx.doi.org/10.1038/s41598-021-94995-8
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