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ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population
BACKGROUND: Excision repair cross-complementing group 1 (ERCC1) was considered a potential candidate gene for ischemic stroke, and its polymorphisms might be associated with the susceptibility to ischemic stroke. METHODS: A total of 513 patients with ischemic stroke and 550 control subjects were rec...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878395/ https://www.ncbi.nlm.nih.gov/pubmed/36712419 http://dx.doi.org/10.3389/fneur.2022.998428 |
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author | Deng, Xiao-Dong Ke, Jian-Lin Chen, Tai-Yu Gao, Qin Zhao, Zhuo-Lin Zhang, Wei Liu, Huan Xiang, Ming-Liang Wang, Li-Zhen Ma, Ying Liu, Yun |
author_facet | Deng, Xiao-Dong Ke, Jian-Lin Chen, Tai-Yu Gao, Qin Zhao, Zhuo-Lin Zhang, Wei Liu, Huan Xiang, Ming-Liang Wang, Li-Zhen Ma, Ying Liu, Yun |
author_sort | Deng, Xiao-Dong |
collection | PubMed |
description | BACKGROUND: Excision repair cross-complementing group 1 (ERCC1) was considered a potential candidate gene for ischemic stroke, and its polymorphisms might be associated with the susceptibility to ischemic stroke. METHODS: A total of 513 patients with ischemic stroke and 550 control subjects were recruited. The expression levels of ERCC1 messenger RNA (mRNA) in peripheral blood mononuclear cells and its protein in plasma were detected by quantitative real-time PCR (qPCR) and enzyme-linked immunosorbent assay (ELISA), respectively. Rs3212986 polymorphism of ERCC1 was detected by PCR-restriction fragment length polymorphism (RFLP-PCR) and was confirmed by sequencing. The association between the ERCC1 rs3212986 polymorphism or its expression and ischemic stroke was further analyzed. RESULTS: The ERCC1 mRNA level in patients with ischemic stroke was lower than that in the control group (P < 0.05). However, the ERCC1 protein level in patients with ischemic stroke was higher than that in the control group (P < 0.05). The A allele of rs3212986 was associated with increased ischemic stroke risk (OR = 1.287, 95% CI = 1.076–1.540, P = 0.006). The association between rs3212986 polymorphism and ischemic stroke susceptibility was found in both recessive (OR = 2.638, 95% CI = 1.744–3.989, P < 0.001) and additive models (OR = 1.309, 95% CI = 1.028–1.667, P = 0.031), respectively. Similar results were obtained in the recessive model (OR = 2.015, 95% CI = 1.087–3.704, P = 0.026) after adjusting for demographic information and other variables. Additionally, the level of ERCC1 mRNA in the CC/CA genotype was higher than that in the AA genotype (P < 0.05). CONCLUSION: It was suggested that the ERCC1 rs3212986 polymorphism was associated with ischemic stroke susceptibility in a Chinese Han population and that an A allele of rs3212986 was related to increased ischemic stroke risk. The altered ERCC1 expression level caused by the rs3212986 polymorphism might participate in the pathophysiological process of ischemic stroke. |
format | Online Article Text |
id | pubmed-9878395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98783952023-01-27 ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population Deng, Xiao-Dong Ke, Jian-Lin Chen, Tai-Yu Gao, Qin Zhao, Zhuo-Lin Zhang, Wei Liu, Huan Xiang, Ming-Liang Wang, Li-Zhen Ma, Ying Liu, Yun Front Neurol Neurology BACKGROUND: Excision repair cross-complementing group 1 (ERCC1) was considered a potential candidate gene for ischemic stroke, and its polymorphisms might be associated with the susceptibility to ischemic stroke. METHODS: A total of 513 patients with ischemic stroke and 550 control subjects were recruited. The expression levels of ERCC1 messenger RNA (mRNA) in peripheral blood mononuclear cells and its protein in plasma were detected by quantitative real-time PCR (qPCR) and enzyme-linked immunosorbent assay (ELISA), respectively. Rs3212986 polymorphism of ERCC1 was detected by PCR-restriction fragment length polymorphism (RFLP-PCR) and was confirmed by sequencing. The association between the ERCC1 rs3212986 polymorphism or its expression and ischemic stroke was further analyzed. RESULTS: The ERCC1 mRNA level in patients with ischemic stroke was lower than that in the control group (P < 0.05). However, the ERCC1 protein level in patients with ischemic stroke was higher than that in the control group (P < 0.05). The A allele of rs3212986 was associated with increased ischemic stroke risk (OR = 1.287, 95% CI = 1.076–1.540, P = 0.006). The association between rs3212986 polymorphism and ischemic stroke susceptibility was found in both recessive (OR = 2.638, 95% CI = 1.744–3.989, P < 0.001) and additive models (OR = 1.309, 95% CI = 1.028–1.667, P = 0.031), respectively. Similar results were obtained in the recessive model (OR = 2.015, 95% CI = 1.087–3.704, P = 0.026) after adjusting for demographic information and other variables. Additionally, the level of ERCC1 mRNA in the CC/CA genotype was higher than that in the AA genotype (P < 0.05). CONCLUSION: It was suggested that the ERCC1 rs3212986 polymorphism was associated with ischemic stroke susceptibility in a Chinese Han population and that an A allele of rs3212986 was related to increased ischemic stroke risk. The altered ERCC1 expression level caused by the rs3212986 polymorphism might participate in the pathophysiological process of ischemic stroke. Frontiers Media S.A. 2023-01-12 /pmc/articles/PMC9878395/ /pubmed/36712419 http://dx.doi.org/10.3389/fneur.2022.998428 Text en Copyright © 2023 Deng, Ke, Chen, Gao, Zhao, Zhang, Liu, Xiang, Wang, Ma and Liu. 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 Deng, Xiao-Dong Ke, Jian-Lin Chen, Tai-Yu Gao, Qin Zhao, Zhuo-Lin Zhang, Wei Liu, Huan Xiang, Ming-Liang Wang, Li-Zhen Ma, Ying Liu, Yun ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population |
title | ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population |
title_full | ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population |
title_fullStr | ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population |
title_full_unstemmed | ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population |
title_short | ERCC1 polymorphism and its expression associated with ischemic stroke in Chinese population |
title_sort | ercc1 polymorphism and its expression associated with ischemic stroke in chinese population |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9878395/ https://www.ncbi.nlm.nih.gov/pubmed/36712419 http://dx.doi.org/10.3389/fneur.2022.998428 |
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