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Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study

All blood cells (white blood cells [WBC], red blood cells [RBC] and platelets) can play a role in atherosclerosis. Complete blood count (CBC) is widely available in clinical practice but utility as potential risk factors for cardiovascular disease (CVD) is uncertain. Our aim was to assess the associ...

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Autores principales: Lassale, Camille, Curtis, Alyscia, Abete, Itziar, van der Schouw, Yvonne. T., Verschuren, W. M. Monique, Lu, Yunxia, Bueno-de-Mesquita, H. B(as).
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818488/
https://www.ncbi.nlm.nih.gov/pubmed/29459661
http://dx.doi.org/10.1038/s41598-018-21661-x
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author Lassale, Camille
Curtis, Alyscia
Abete, Itziar
van der Schouw, Yvonne. T.
Verschuren, W. M. Monique
Lu, Yunxia
Bueno-de-Mesquita, H. B(as).
author_facet Lassale, Camille
Curtis, Alyscia
Abete, Itziar
van der Schouw, Yvonne. T.
Verschuren, W. M. Monique
Lu, Yunxia
Bueno-de-Mesquita, H. B(as).
author_sort Lassale, Camille
collection PubMed
description All blood cells (white blood cells [WBC], red blood cells [RBC] and platelets) can play a role in atherosclerosis. Complete blood count (CBC) is widely available in clinical practice but utility as potential risk factors for cardiovascular disease (CVD) is uncertain. Our aim was to assess the associations of pre-diagnostic CBC with incidence of CVD in 14,362 adults free of CVD and aged 47.8 (±11.7) years at baseline, followed-up for 11.4 years (992 incident cases). Cox proportional hazards regressions were used to estimate HRs and 95%CI. Comparing the top (T3) to bottom (T1) tertile, increased total WBC, lymphocyte, monocyte and neutrophil counts were associated with higher CVD risk: 1.31 (1.10; 1.55), 1.20 (1.02; 1.41), 1.21 (1.03; 1.41) and 1.24 (1.05; 1.47), as well as mean corpuscular volume (MCV: 1.23 [1.04; 1.46]) and red cell distribution width (RDW: 1.22 [1.03; 1.44]). Platelets displayed an association for count values above the clinically normal range: 1.49 (1.00; 2.22). To conclude, total and differential WBC count, MCV, RDW and platelet count likely play a role in the aetiology of CVD but only WBC provide a modest improvement for the prediction of 10-year CVD risk over traditional CVD risk factors in a general population.
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spelling pubmed-58184882018-02-26 Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study Lassale, Camille Curtis, Alyscia Abete, Itziar van der Schouw, Yvonne. T. Verschuren, W. M. Monique Lu, Yunxia Bueno-de-Mesquita, H. B(as). Sci Rep Article All blood cells (white blood cells [WBC], red blood cells [RBC] and platelets) can play a role in atherosclerosis. Complete blood count (CBC) is widely available in clinical practice but utility as potential risk factors for cardiovascular disease (CVD) is uncertain. Our aim was to assess the associations of pre-diagnostic CBC with incidence of CVD in 14,362 adults free of CVD and aged 47.8 (±11.7) years at baseline, followed-up for 11.4 years (992 incident cases). Cox proportional hazards regressions were used to estimate HRs and 95%CI. Comparing the top (T3) to bottom (T1) tertile, increased total WBC, lymphocyte, monocyte and neutrophil counts were associated with higher CVD risk: 1.31 (1.10; 1.55), 1.20 (1.02; 1.41), 1.21 (1.03; 1.41) and 1.24 (1.05; 1.47), as well as mean corpuscular volume (MCV: 1.23 [1.04; 1.46]) and red cell distribution width (RDW: 1.22 [1.03; 1.44]). Platelets displayed an association for count values above the clinically normal range: 1.49 (1.00; 2.22). To conclude, total and differential WBC count, MCV, RDW and platelet count likely play a role in the aetiology of CVD but only WBC provide a modest improvement for the prediction of 10-year CVD risk over traditional CVD risk factors in a general population. Nature Publishing Group UK 2018-02-19 /pmc/articles/PMC5818488/ /pubmed/29459661 http://dx.doi.org/10.1038/s41598-018-21661-x Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lassale, Camille
Curtis, Alyscia
Abete, Itziar
van der Schouw, Yvonne. T.
Verschuren, W. M. Monique
Lu, Yunxia
Bueno-de-Mesquita, H. B(as).
Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study
title Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study
title_full Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study
title_fullStr Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study
title_full_unstemmed Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study
title_short Elements of the complete blood count associated with cardiovascular disease incidence: Findings from the EPIC-NL cohort study
title_sort elements of the complete blood count associated with cardiovascular disease incidence: findings from the epic-nl cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818488/
https://www.ncbi.nlm.nih.gov/pubmed/29459661
http://dx.doi.org/10.1038/s41598-018-21661-x
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