4.6 Article

Visceral Adiposity and Risk of Stroke: A Mendelian Randomization Study

期刊

FRONTIERS IN NEUROLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fneur.2022.804851

关键词

visceral adipose tissue (VAT); ischemic stroke; intracranial hemorrhage (ICH); mendelian randomization (MR); single nucleotide polymorphism (SNP)

资金

  1. Ministry of Science and Technology of the People's Republic of China [2016YFC1301700]
  2. Capital Medical University Science Program for Fostering Young Scholars [1210020222]
  3. Xuanwu Hospital Science Program for Fostering Young Scholars [QNPY2020010]

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This study suggests a causal relationship between VAT and ischemic stroke based on a large-scale MR study. VAT showed a significant causal association with ischemic stroke, particularly with cardioembolic stroke, small-vessel stroke, and large-artery atherosclerotic stroke. The findings may lead to the development of new genetic therapeutic strategies for different subtypes of ischemic stroke.
PurposeIn 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. MethodsBased 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. ResultsVAT 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). ConclusionsThis 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.

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