Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.

Estrogen is involved in neuron plasticity and can promote neuronal survival in stroke. Its actions are mostly exerted via estrogen receptor alpha (ERα). Previous animal studies have shown that ERα is upregulated by DNA demethylation following ischemic injury. This study investigated the methylation...

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Main Authors: Hsiu-Fen Lin, Edward Hsi, Yi-Chu Liao, Brian Chhor, Jessica Hung, Suh-Hang H Juo, Ruey-Tay Lin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4589317?pdf=render
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spelling doaj-019a004f6e10404abfd594d94fd7bb672020-11-24T21:10:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01109e013960810.1371/journal.pone.0139608Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.Hsiu-Fen LinEdward HsiYi-Chu LiaoBrian ChhorJessica HungSuh-Hang H JuoRuey-Tay LinEstrogen is involved in neuron plasticity and can promote neuronal survival in stroke. Its actions are mostly exerted via estrogen receptor alpha (ERα). Previous animal studies have shown that ERα is upregulated by DNA demethylation following ischemic injury. This study investigated the methylation levels in the ERα promoter in the peripheral blood of ischemic stroke patients.The study included 201 ischemic stroke patients, and 217 age- and sex-comparable healthy controls. The quantitative methylation level in the 14 CpG sites of the ERα promoter was measured by pyrosequencing in each participant. Multivariate regression model was used to adjust for stroke traditional risk factors. Stroke subtypes and sex-specific analysis were also conducted.The results demonstrated that the stroke cases had a lower ERα methylation level than controls in all 14 CpG sites, and site 13 and site 14 had significant adjusted p-values of 0.035 and 0.026, respectively. Stroke subtypes analysis showed that large-artery atherosclerosis and cardio-embolic subtypes had significantly lower methylation levels than the healthy controls at CpG site 5, site 9, site 12, site 13 and site 14 with adjusted p = 0.039, 0.009, 0.025, 0.046 and 0.027 respectively. However, the methylation level for the patients with small vessel subtype was not significant. We combined the methylation data from the above five sites for further sex-specific analysis. The results showed that the significant association only existed in women (adjusted p = 0.011), but not in men (adjusted p = 0.300).Female stroke cases have lower ERα methylation levels than those in the controls, especially in large-artery and cardio-embolic stroke subtypes. The study implies that women suffering from ischemic stroke of specific subtype may undergo different protective mechanisms to reduce the brain injury.http://europepmc.org/articles/PMC4589317?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Hsiu-Fen Lin
Edward Hsi
Yi-Chu Liao
Brian Chhor
Jessica Hung
Suh-Hang H Juo
Ruey-Tay Lin
spellingShingle Hsiu-Fen Lin
Edward Hsi
Yi-Chu Liao
Brian Chhor
Jessica Hung
Suh-Hang H Juo
Ruey-Tay Lin
Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.
PLoS ONE
author_facet Hsiu-Fen Lin
Edward Hsi
Yi-Chu Liao
Brian Chhor
Jessica Hung
Suh-Hang H Juo
Ruey-Tay Lin
author_sort Hsiu-Fen Lin
title Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.
title_short Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.
title_full Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.
title_fullStr Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.
title_full_unstemmed Demethylation of Circulating Estrogen Receptor Alpha Gene in Cerebral Ischemic Stroke.
title_sort demethylation of circulating estrogen receptor alpha gene in cerebral ischemic stroke.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Estrogen is involved in neuron plasticity and can promote neuronal survival in stroke. Its actions are mostly exerted via estrogen receptor alpha (ERα). Previous animal studies have shown that ERα is upregulated by DNA demethylation following ischemic injury. This study investigated the methylation levels in the ERα promoter in the peripheral blood of ischemic stroke patients.The study included 201 ischemic stroke patients, and 217 age- and sex-comparable healthy controls. The quantitative methylation level in the 14 CpG sites of the ERα promoter was measured by pyrosequencing in each participant. Multivariate regression model was used to adjust for stroke traditional risk factors. Stroke subtypes and sex-specific analysis were also conducted.The results demonstrated that the stroke cases had a lower ERα methylation level than controls in all 14 CpG sites, and site 13 and site 14 had significant adjusted p-values of 0.035 and 0.026, respectively. Stroke subtypes analysis showed that large-artery atherosclerosis and cardio-embolic subtypes had significantly lower methylation levels than the healthy controls at CpG site 5, site 9, site 12, site 13 and site 14 with adjusted p = 0.039, 0.009, 0.025, 0.046 and 0.027 respectively. However, the methylation level for the patients with small vessel subtype was not significant. We combined the methylation data from the above five sites for further sex-specific analysis. The results showed that the significant association only existed in women (adjusted p = 0.011), but not in men (adjusted p = 0.300).Female stroke cases have lower ERα methylation levels than those in the controls, especially in large-artery and cardio-embolic stroke subtypes. The study implies that women suffering from ischemic stroke of specific subtype may undergo different protective mechanisms to reduce the brain injury.
url http://europepmc.org/articles/PMC4589317?pdf=render
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