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White blood cells and coronary heart disease: A mendelian randomization study

Background: The causal direction and magnitude of the associations between blood cell count and coronary heart disease (CHD) remain uncertain due to susceptibility of reverse causation and confounding. This study aimed to investigate the associations between blood cell count and CHD using Mendelian...

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Autores principales: Zhao, Qiuping, Liu, Rongmei, Chen, Hui, Yang, Xiaomo, Dong, Jiajia, Bai, Minfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941875/
https://www.ncbi.nlm.nih.gov/pubmed/36824433
http://dx.doi.org/10.3389/fgene.2023.1127820
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author Zhao, Qiuping
Liu, Rongmei
Chen, Hui
Yang, Xiaomo
Dong, Jiajia
Bai, Minfu
author_facet Zhao, Qiuping
Liu, Rongmei
Chen, Hui
Yang, Xiaomo
Dong, Jiajia
Bai, Minfu
author_sort Zhao, Qiuping
collection PubMed
description Background: The causal direction and magnitude of the associations between blood cell count and coronary heart disease (CHD) remain uncertain due to susceptibility of reverse causation and confounding. This study aimed to investigate the associations between blood cell count and CHD using Mendelian randomization (MR). Methods: In this two-sample MR study, we identified independent blood cell count associated genetic variants from a genome-wide association studies (GWAS) among European ancestry individuals. Summary level data of CHD was obtained from a GWAS consisting of 547261 subjects. Methods of inverse variance weighted (IVW), Mendelian Randomization-Egger (MR-Egger), weighted median, and outlier test (MR-PRESSO) were conducted to investigate the associations between blood cell and CHD. Results: Among all cardiovascular outcomes of interest, blood cell counts were only associated with CHD. Our findings indicated that white blood cell count and neutrophil cell count were significantly associated with increased risk of CHD [odds ratio (OR) = 1.07, 95% confidence interval (CI), 1.01–1.14; OR = 1.09, 1.02–1.16). However, there was no significant association between monocyte cell count, basophil cell count, lymphocyte cell count, eosinophil cell count, and CHD (p > 0.05). The results after excluding outliers were consistent with main results and the sensitivity analyses showed no evidence of pleiotropy (MR-Egger intercept, p > 0.05). Conclusion: Our MR study suggested that greater white blood cell count and neutrophil cell count were associated with a higher risk of CHD. Future studies are still warranted to validate the results and investigate the mechanisms underlying these associations.
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spelling pubmed-99418752023-02-22 White blood cells and coronary heart disease: A mendelian randomization study Zhao, Qiuping Liu, Rongmei Chen, Hui Yang, Xiaomo Dong, Jiajia Bai, Minfu Front Genet Genetics Background: The causal direction and magnitude of the associations between blood cell count and coronary heart disease (CHD) remain uncertain due to susceptibility of reverse causation and confounding. This study aimed to investigate the associations between blood cell count and CHD using Mendelian randomization (MR). Methods: In this two-sample MR study, we identified independent blood cell count associated genetic variants from a genome-wide association studies (GWAS) among European ancestry individuals. Summary level data of CHD was obtained from a GWAS consisting of 547261 subjects. Methods of inverse variance weighted (IVW), Mendelian Randomization-Egger (MR-Egger), weighted median, and outlier test (MR-PRESSO) were conducted to investigate the associations between blood cell and CHD. Results: Among all cardiovascular outcomes of interest, blood cell counts were only associated with CHD. Our findings indicated that white blood cell count and neutrophil cell count were significantly associated with increased risk of CHD [odds ratio (OR) = 1.07, 95% confidence interval (CI), 1.01–1.14; OR = 1.09, 1.02–1.16). However, there was no significant association between monocyte cell count, basophil cell count, lymphocyte cell count, eosinophil cell count, and CHD (p > 0.05). The results after excluding outliers were consistent with main results and the sensitivity analyses showed no evidence of pleiotropy (MR-Egger intercept, p > 0.05). Conclusion: Our MR study suggested that greater white blood cell count and neutrophil cell count were associated with a higher risk of CHD. Future studies are still warranted to validate the results and investigate the mechanisms underlying these associations. Frontiers Media S.A. 2023-02-07 /pmc/articles/PMC9941875/ /pubmed/36824433 http://dx.doi.org/10.3389/fgene.2023.1127820 Text en Copyright © 2023 Zhao, Liu, Chen, Yang, Dong and Bai. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Zhao, Qiuping
Liu, Rongmei
Chen, Hui
Yang, Xiaomo
Dong, Jiajia
Bai, Minfu
White blood cells and coronary heart disease: A mendelian randomization study
title White blood cells and coronary heart disease: A mendelian randomization study
title_full White blood cells and coronary heart disease: A mendelian randomization study
title_fullStr White blood cells and coronary heart disease: A mendelian randomization study
title_full_unstemmed White blood cells and coronary heart disease: A mendelian randomization study
title_short White blood cells and coronary heart disease: A mendelian randomization study
title_sort white blood cells and coronary heart disease: a mendelian randomization study
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941875/
https://www.ncbi.nlm.nih.gov/pubmed/36824433
http://dx.doi.org/10.3389/fgene.2023.1127820
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