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Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes

INTRODUCTION: Elevated red cell distribution width (RDW) has been associated with a range of health outcomes. This study aims to examine prognostic and etiological roles of RDW levels, both phenotypic and genetic predisposition, in predicting cardiovascular outcomes, diabetes, chronic kidney disease...

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Autores principales: Pan, Jingxue, Sun, Jiangming, Goncalves, Isabel, Kessler, Michael, Hao, Yan, Engström, Gunnar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694461/
http://dx.doi.org/10.3389/fcvm.2023.1294218
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author Pan, Jingxue
Sun, Jiangming
Goncalves, Isabel
Kessler, Michael
Hao, Yan
Engström, Gunnar
author_facet Pan, Jingxue
Sun, Jiangming
Goncalves, Isabel
Kessler, Michael
Hao, Yan
Engström, Gunnar
author_sort Pan, Jingxue
collection PubMed
description INTRODUCTION: Elevated red cell distribution width (RDW) has been associated with a range of health outcomes. This study aims to examine prognostic and etiological roles of RDW levels, both phenotypic and genetic predisposition, in predicting cardiovascular outcomes, diabetes, chronic kidney disease (CKD) and mortality. METHODS: We studied 27,141 middle-aged adults from the Malmö Diet and Cancer study (MDCS) with a mean follow up of 21 years. RDW was measured with a hematology analyzer on whole blood samples. Polygenic scores for RDW (PGS-RDW) were constructed for each participant using genetic data in MDCS and published summary statistics from genome-wide association study of RDW (n = 408,112). Cox proportional hazards regression was used to assess associations between RDW, PGS-RDW and cardiovascular outcomes, diabetes, CKD and mortality, respectively. RESULTS: PGS-RDW was significantly associated with RDW (Pearson's correlation coefficient = 0.133, p < 0.001). RDW was significantly associated with incidence of stroke (hazard ratio (HR) per 1 standard deviation = 1.06, 95% confidence interval (CI): 1.02–1.10, p = 0.003), atrial fibrillation (HR = 1.09, 95% CI: 1.06–1.12, p < 0.001), heart failure (HR = 1.13, 95% CI: 1.08–1.19, p < 0.001), venous thromboembolism (HR = 1.21, 95% CI: 1.15–1.28, p < 0.001), diabetes (HR = 0.87, 95% CI: 0.84–0.90, p < 0.001), CKD (HR = 1.08, 95% CI: 1.03–1.13, p = 0.004) and all-cause mortality (HR = 1.18, 95% CI: 1.16–1.20, p < 0.001). However, PGS-RDW was significantly associated with incidence of diabetes (HR = 0.96, 95% CI: 0.94–0.99, p = 0.01), but not with any other tested outcomes. DISCUSSION: RDW is associated with mortality and incidence of cardiovascular diseases, but a significant association between genetically determined RDW and incident cardiovascular diseases were not observed. However, both RDW and PGS-RDW were inversely associated with incidence of diabetes, suggesting a putative causal relationship. The relationship with incidence of diabetes needs to be further studied.
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spelling pubmed-106944612023-12-05 Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes Pan, Jingxue Sun, Jiangming Goncalves, Isabel Kessler, Michael Hao, Yan Engström, Gunnar Front Cardiovasc Med Cardiovascular Medicine INTRODUCTION: Elevated red cell distribution width (RDW) has been associated with a range of health outcomes. This study aims to examine prognostic and etiological roles of RDW levels, both phenotypic and genetic predisposition, in predicting cardiovascular outcomes, diabetes, chronic kidney disease (CKD) and mortality. METHODS: We studied 27,141 middle-aged adults from the Malmö Diet and Cancer study (MDCS) with a mean follow up of 21 years. RDW was measured with a hematology analyzer on whole blood samples. Polygenic scores for RDW (PGS-RDW) were constructed for each participant using genetic data in MDCS and published summary statistics from genome-wide association study of RDW (n = 408,112). Cox proportional hazards regression was used to assess associations between RDW, PGS-RDW and cardiovascular outcomes, diabetes, CKD and mortality, respectively. RESULTS: PGS-RDW was significantly associated with RDW (Pearson's correlation coefficient = 0.133, p < 0.001). RDW was significantly associated with incidence of stroke (hazard ratio (HR) per 1 standard deviation = 1.06, 95% confidence interval (CI): 1.02–1.10, p = 0.003), atrial fibrillation (HR = 1.09, 95% CI: 1.06–1.12, p < 0.001), heart failure (HR = 1.13, 95% CI: 1.08–1.19, p < 0.001), venous thromboembolism (HR = 1.21, 95% CI: 1.15–1.28, p < 0.001), diabetes (HR = 0.87, 95% CI: 0.84–0.90, p < 0.001), CKD (HR = 1.08, 95% CI: 1.03–1.13, p = 0.004) and all-cause mortality (HR = 1.18, 95% CI: 1.16–1.20, p < 0.001). However, PGS-RDW was significantly associated with incidence of diabetes (HR = 0.96, 95% CI: 0.94–0.99, p = 0.01), but not with any other tested outcomes. DISCUSSION: RDW is associated with mortality and incidence of cardiovascular diseases, but a significant association between genetically determined RDW and incident cardiovascular diseases were not observed. However, both RDW and PGS-RDW were inversely associated with incidence of diabetes, suggesting a putative causal relationship. The relationship with incidence of diabetes needs to be further studied. Frontiers Media S.A. 2023-11-20 /pmc/articles/PMC10694461/ http://dx.doi.org/10.3389/fcvm.2023.1294218 Text en © 2023 Pan, Sun, Goncalves, Kessler, Hao and Engström. 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) (https://creativecommons.org/licenses/by/4.0/) . 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 Cardiovascular Medicine
Pan, Jingxue
Sun, Jiangming
Goncalves, Isabel
Kessler, Michael
Hao, Yan
Engström, Gunnar
Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes
title Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes
title_full Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes
title_fullStr Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes
title_full_unstemmed Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes
title_short Red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes
title_sort red cell distribution width and its polygenic score in relation to mortality and cardiometabolic outcomes
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694461/
http://dx.doi.org/10.3389/fcvm.2023.1294218
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