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Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up

BACKGROUND: Ischaemic heart disease (IHD) often develops after decades of preceding subclinical coronary atherosclerosis. Biomarkers are useful prognostic predictors of IHD, but their long-term predictive value in a general population has not been adequately studied. PURPOSE: To investigate the earl...

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Autores principales: Sakalaki, Maria, Hansson, Per-Olof, Rosengren, Annika, Thunström, Erik, Pivodic, Aldina, Fu, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851898/
https://www.ncbi.nlm.nih.gov/pubmed/33530933
http://dx.doi.org/10.1186/s12872-021-01886-x
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author Sakalaki, Maria
Hansson, Per-Olof
Rosengren, Annika
Thunström, Erik
Pivodic, Aldina
Fu, Michael
author_facet Sakalaki, Maria
Hansson, Per-Olof
Rosengren, Annika
Thunström, Erik
Pivodic, Aldina
Fu, Michael
author_sort Sakalaki, Maria
collection PubMed
description BACKGROUND: Ischaemic heart disease (IHD) often develops after decades of preceding subclinical coronary atherosclerosis. Biomarkers are useful prognostic predictors of IHD, but their long-term predictive value in a general population has not been adequately studied. PURPOSE: To investigate the early predictive value of multi-modality biomarkers in addition to clinical risk factors in incident IHD in a random male general population sample followed from 50 to 71 years of age. METHOD: “The Study of Men Born in 1943” is a longitudinal cohort study during follow-up. All the men underwent a baseline examination in 1993, where a panel of biomarkers were analysed and incident IHD was registered during 21-year follow-ups. RESULTS: Of 739 participants, 97 men (13.1%) developed an IHD event. For time to first occurrence of IHD, univariable analyses showed that elevated levels of high sensitivity troponin T (hs-TNT), high sensitivity-C reactive protein (hs-CRP) and interleukin-6 (IL-6) were significant predictors of IHD. In addition, a high number of biomarkers with elevated levels (hs-TNT > 10 ng/L, hs-CRP > 1 mg/L, IL-6 > 8 ng/L and N-terminal pro b-type natriuretic peptide (NT-proBNP) > 100 pg/mL) increased predictive ability. In univariable and multivariable analysis high-density lipoprotein-cholesterol (HDL-C) had the highest predictive ability. Hs-TNT provided better predictive ability than smoking, body mass index and glucose, and was an independent significant predictor when adjusted for HDL-C, total cholesterol and hypertension. Addition of biomarkers on top of clinical risk factors provided significantly better prediction as tested by likelihood ratio test (p = 0.033), but did not significantly enhance the model’s discriminative ability However, it appeared contributing to higher sensitivity in the late phase of follow-up. CONCLUSION: In this random, middle-aged male population sample, the addition of biomarker hs-TNT was an independent significant predictor of IHD and significantly improved prediction, indicating the probability of a better prediction of long-term risk of IHD in a low-risk population. Trial registration: The study is registered at Clinical Trials.gov Identifier number: NCT03138122
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spelling pubmed-78518982021-02-03 Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up Sakalaki, Maria Hansson, Per-Olof Rosengren, Annika Thunström, Erik Pivodic, Aldina Fu, Michael BMC Cardiovasc Disord Research Article BACKGROUND: Ischaemic heart disease (IHD) often develops after decades of preceding subclinical coronary atherosclerosis. Biomarkers are useful prognostic predictors of IHD, but their long-term predictive value in a general population has not been adequately studied. PURPOSE: To investigate the early predictive value of multi-modality biomarkers in addition to clinical risk factors in incident IHD in a random male general population sample followed from 50 to 71 years of age. METHOD: “The Study of Men Born in 1943” is a longitudinal cohort study during follow-up. All the men underwent a baseline examination in 1993, where a panel of biomarkers were analysed and incident IHD was registered during 21-year follow-ups. RESULTS: Of 739 participants, 97 men (13.1%) developed an IHD event. For time to first occurrence of IHD, univariable analyses showed that elevated levels of high sensitivity troponin T (hs-TNT), high sensitivity-C reactive protein (hs-CRP) and interleukin-6 (IL-6) were significant predictors of IHD. In addition, a high number of biomarkers with elevated levels (hs-TNT > 10 ng/L, hs-CRP > 1 mg/L, IL-6 > 8 ng/L and N-terminal pro b-type natriuretic peptide (NT-proBNP) > 100 pg/mL) increased predictive ability. In univariable and multivariable analysis high-density lipoprotein-cholesterol (HDL-C) had the highest predictive ability. Hs-TNT provided better predictive ability than smoking, body mass index and glucose, and was an independent significant predictor when adjusted for HDL-C, total cholesterol and hypertension. Addition of biomarkers on top of clinical risk factors provided significantly better prediction as tested by likelihood ratio test (p = 0.033), but did not significantly enhance the model’s discriminative ability However, it appeared contributing to higher sensitivity in the late phase of follow-up. CONCLUSION: In this random, middle-aged male population sample, the addition of biomarker hs-TNT was an independent significant predictor of IHD and significantly improved prediction, indicating the probability of a better prediction of long-term risk of IHD in a low-risk population. Trial registration: The study is registered at Clinical Trials.gov Identifier number: NCT03138122 BioMed Central 2021-02-02 /pmc/articles/PMC7851898/ /pubmed/33530933 http://dx.doi.org/10.1186/s12872-021-01886-x Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Sakalaki, Maria
Hansson, Per-Olof
Rosengren, Annika
Thunström, Erik
Pivodic, Aldina
Fu, Michael
Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up
title Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up
title_full Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up
title_fullStr Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up
title_full_unstemmed Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up
title_short Multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up
title_sort multi-modality biomarkers in the early prediction of ischaemic heart disease in middle-aged men during a 21-year follow-up
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851898/
https://www.ncbi.nlm.nih.gov/pubmed/33530933
http://dx.doi.org/10.1186/s12872-021-01886-x
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