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Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study
PURPOSE: In recent years, metabolic syndrome has risen in prevalence and brought a heavy disease burden to modern society. As the representative aspect of metabolic syndrome, obesity has been shown to be related to an increased risk of stroke. Given that visceral adipose tissue (VAT) forms the funda...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035635/ https://www.ncbi.nlm.nih.gov/pubmed/35481268 http://dx.doi.org/10.3389/fneur.2022.804851 |
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author | Xu, Ran Hu, Xinzhi Wang, Tao Yang, Yutong Jiang, Nan Luo, Jichang Zhang, Xiao Patel, Aman B. Dmytriw, Adam A. Jiao, Liqun |
author_facet | Xu, Ran Hu, Xinzhi Wang, Tao Yang, Yutong Jiang, Nan Luo, Jichang Zhang, Xiao Patel, Aman B. Dmytriw, Adam A. Jiao, Liqun |
author_sort | Xu, Ran |
collection | PubMed |
description | PURPOSE: In recent years, metabolic syndrome has risen in prevalence and brought a heavy disease burden to modern society. As the representative aspect of metabolic syndrome, obesity has been shown to be related to an increased risk of stroke. Given that visceral adipose tissue (VAT) forms the fundamental basis of central obesity, we sought to explore a causal relationship between VAT and stroke by using mendelian randomization (MR) methods. METHODS: Based on two large genome-wide association studies (GWAS) including 325,153 and 35,762 cases of VAT and stroke, respectively, we conducted a MR study which has the inherent advantage of reducing the noise of confounding and reverse causation. RESULTS: VAT had a significant causal association with ischemic stroke (OR, per 1kg increase in VAT mass, 1.30; 95% CI, 1.18 ~ 1.45; P = 5.87E-07) as opposed to intracranial hemorrhage (ICH) (OR, 1.15; 95% CI, 0.70 ~ 1.88, P = 5.81E-01) as evaluated with inverse-variance weighting (IVW). Regarding subtypes of ischemic stroke, there was a significant causal effect for cardioembolic stroke (OR, 1.34; 95% CI, 1.13 ~ 1.58, P = 8.07E-04), and potential causal effect for small-vessel stroke (OR, 1.32; 95% CI, 1.06 ~ 1.65, P = 1.39E-02) and large-artery atherosclerotic stroke (OR, 1.33; 95% CI, 1.03 ~ 1.70, P = 2.59E-02). CONCLUSIONS: This study provides potential evidence for a causal role of VAT in ischemic stroke and could suggest novel genetical therapeutic strategies for distinct subtypes of ischemic stroke. |
format | Online Article Text |
id | pubmed-9035635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90356352022-04-26 Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study Xu, Ran Hu, Xinzhi Wang, Tao Yang, Yutong Jiang, Nan Luo, Jichang Zhang, Xiao Patel, Aman B. Dmytriw, Adam A. Jiao, Liqun Front Neurol Neurology PURPOSE: In recent years, metabolic syndrome has risen in prevalence and brought a heavy disease burden to modern society. As the representative aspect of metabolic syndrome, obesity has been shown to be related to an increased risk of stroke. Given that visceral adipose tissue (VAT) forms the fundamental basis of central obesity, we sought to explore a causal relationship between VAT and stroke by using mendelian randomization (MR) methods. METHODS: Based on two large genome-wide association studies (GWAS) including 325,153 and 35,762 cases of VAT and stroke, respectively, we conducted a MR study which has the inherent advantage of reducing the noise of confounding and reverse causation. RESULTS: VAT had a significant causal association with ischemic stroke (OR, per 1kg increase in VAT mass, 1.30; 95% CI, 1.18 ~ 1.45; P = 5.87E-07) as opposed to intracranial hemorrhage (ICH) (OR, 1.15; 95% CI, 0.70 ~ 1.88, P = 5.81E-01) as evaluated with inverse-variance weighting (IVW). Regarding subtypes of ischemic stroke, there was a significant causal effect for cardioembolic stroke (OR, 1.34; 95% CI, 1.13 ~ 1.58, P = 8.07E-04), and potential causal effect for small-vessel stroke (OR, 1.32; 95% CI, 1.06 ~ 1.65, P = 1.39E-02) and large-artery atherosclerotic stroke (OR, 1.33; 95% CI, 1.03 ~ 1.70, P = 2.59E-02). CONCLUSIONS: This study provides potential evidence for a causal role of VAT in ischemic stroke and could suggest novel genetical therapeutic strategies for distinct subtypes of ischemic stroke. Frontiers Media S.A. 2022-04-11 /pmc/articles/PMC9035635/ /pubmed/35481268 http://dx.doi.org/10.3389/fneur.2022.804851 Text en Copyright © 2022 Xu, Hu, Wang, Yang, Jiang, Luo, Zhang, Patel, Dmytriw and Jiao. 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 | Neurology Xu, Ran Hu, Xinzhi Wang, Tao Yang, Yutong Jiang, Nan Luo, Jichang Zhang, Xiao Patel, Aman B. Dmytriw, Adam A. Jiao, Liqun Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study |
title | Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study |
title_full | Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study |
title_fullStr | Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study |
title_full_unstemmed | Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study |
title_short | Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study |
title_sort | visceral adiposity and risk of stroke: a mendelian randomization study |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035635/ https://www.ncbi.nlm.nih.gov/pubmed/35481268 http://dx.doi.org/10.3389/fneur.2022.804851 |
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