2022
DOI: 10.3389/fgene.2022.844141
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Association of DNA Methylation Patterns in 7 Novel Genes With Ischemic Stroke in the Northern Chinese Population

Abstract: Background: Ischemic stroke is a highly complex disorder. This study aims to identify novel methylation changes in ischemic stroke.Methods: We carried out an epigenome-wide study of ischemic stroke using an Infinium HumanMethylation 850K array (cases:controls = 4:4). 10 CpG sites in 8 candidate genes from gene ontology analytics top-ranked pathway were selected to validate 850K BeadChip results (cases:controls = 20:20). We further qualified the methylation level of promoter regions in 8 candidate genes (cases:… Show more

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Cited by 7 publications
(4 citation statements)
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References 37 publications
(47 reference statements)
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“…Meanwhile, Hongwei Sun reported overexpression of CDH2 in MI vascular smooth muscle cells compared with that in controls 28 . Interestingly, the mesenchymal marker CDH2 was downregulated, while the epithelial marker CDH1 was increased during MI, suggesting that EMT‐related signalling rather than the EMT process is associated with AMI 29 …”
Section: Discussionmentioning
confidence: 99%
“…Meanwhile, Hongwei Sun reported overexpression of CDH2 in MI vascular smooth muscle cells compared with that in controls 28 . Interestingly, the mesenchymal marker CDH2 was downregulated, while the epithelial marker CDH1 was increased during MI, suggesting that EMT‐related signalling rather than the EMT process is associated with AMI 29 …”
Section: Discussionmentioning
confidence: 99%
“…The sixth hub Pcdhb10 encodes a calcium-dependent cell–cell adhesion protein of the cadherin superfamily. PCDHs have been reported to be relevant to epilepsy and neurodegenerative diseases 51 . Defective function of cadherin, such as PCDH19, is known to be related to febrile convulsions and most often patients are drug-resistant to treatment 52 .…”
Section: Discussionmentioning
confidence: 99%
“…Among the identified significant CpG sites differentially associated with changes in both FPG and HbA1c (RYGB vs. IMI), 4 CpG sites including cg18373318 ( SNX18 ), cg26878734 ( LNPK ), cg05994094 ( CCDC178 ) and cg08383526 ( ADAM7 ) showed robust significance after genomic correction. Interestingly, methylation at cg18373318 ( SNX18 ) has been previously shown to be associated with ischemic stroke by a previous EWAS [ 24 ]; ischemic stroke is one of the multiple cardiovascular outcomes observed in individuals with obesity [ 25 ]. The SNX18 gene encodes a member of the sorting nexin family, which are involved in endocytosis and intracellular vesicle trafficking [ 26 ].…”
Section: Discussionmentioning
confidence: 99%