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Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke
It has been demonstrated that phosphodiesterase 4D (PDE4D) genetic polymorphism is associated with ischemic stroke. However, the association between PDE4D gene and prognosis after ischemic stroke remains unknown. We consecutively enrolled ischemic stroke patients admitted to Beijing Tiantan Hospital...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320494/ https://www.ncbi.nlm.nih.gov/pubmed/28225001 http://dx.doi.org/10.1038/srep42914 |
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author | Song, Yan-li Wang, Chun-juan Wu, Yi-ping Lin, Jie Wang, Peng-lian Du, Wan-liang Liu, Li Lin, Jin-xi Wang, Yi-long Wang, Yong-jun Liu, Gai-fen |
author_facet | Song, Yan-li Wang, Chun-juan Wu, Yi-ping Lin, Jie Wang, Peng-lian Du, Wan-liang Liu, Li Lin, Jin-xi Wang, Yi-long Wang, Yong-jun Liu, Gai-fen |
author_sort | Song, Yan-li |
collection | PubMed |
description | It has been demonstrated that phosphodiesterase 4D (PDE4D) genetic polymorphism is associated with ischemic stroke. However, the association between PDE4D gene and prognosis after ischemic stroke remains unknown. We consecutively enrolled ischemic stroke patients admitted to Beijing Tiantan Hospital from October 2009 to December 2013. Clinical, laboratory and imaging data upon admission were collected. All patients were followed up 3 months after stroke onset. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the associations of genetic polymorphisms with 3-month outcome after ischemic stroke and different subtypes, under various genetic models. A total of 1447 patients were enrolled, and 3-month follow-up data were obtained from 1388 (95.92%). Multivariate regression analysis showed that SNP87 of PDE4D gene was associated with increased risk of unfavorable outcome after total ischemic stroke (OR = 1.47, 95%CI 1.12–1.93), as well as stroke due to large-artery atherosclerosis (OR = 1.49, 95%CI 1.04–2.11) and small-artery occlusion (OR = 1.76, 95%CI 1.05–2.96) under a recessive model. No association between SNP83 genotype and poor outcome was found. Overall, this study demonstrated that the TT genotype of SNP87 in PDE4D was associated with increased risk of poor outcome after total ischemic stroke, large-artery atherosclerosis and small-artery occlusion, in a Chinese population. |
format | Online Article Text |
id | pubmed-5320494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53204942017-03-01 Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke Song, Yan-li Wang, Chun-juan Wu, Yi-ping Lin, Jie Wang, Peng-lian Du, Wan-liang Liu, Li Lin, Jin-xi Wang, Yi-long Wang, Yong-jun Liu, Gai-fen Sci Rep Article It has been demonstrated that phosphodiesterase 4D (PDE4D) genetic polymorphism is associated with ischemic stroke. However, the association between PDE4D gene and prognosis after ischemic stroke remains unknown. We consecutively enrolled ischemic stroke patients admitted to Beijing Tiantan Hospital from October 2009 to December 2013. Clinical, laboratory and imaging data upon admission were collected. All patients were followed up 3 months after stroke onset. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to assess the associations of genetic polymorphisms with 3-month outcome after ischemic stroke and different subtypes, under various genetic models. A total of 1447 patients were enrolled, and 3-month follow-up data were obtained from 1388 (95.92%). Multivariate regression analysis showed that SNP87 of PDE4D gene was associated with increased risk of unfavorable outcome after total ischemic stroke (OR = 1.47, 95%CI 1.12–1.93), as well as stroke due to large-artery atherosclerosis (OR = 1.49, 95%CI 1.04–2.11) and small-artery occlusion (OR = 1.76, 95%CI 1.05–2.96) under a recessive model. No association between SNP83 genotype and poor outcome was found. Overall, this study demonstrated that the TT genotype of SNP87 in PDE4D was associated with increased risk of poor outcome after total ischemic stroke, large-artery atherosclerosis and small-artery occlusion, in a Chinese population. Nature Publishing Group 2017-02-22 /pmc/articles/PMC5320494/ /pubmed/28225001 http://dx.doi.org/10.1038/srep42914 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Song, Yan-li Wang, Chun-juan Wu, Yi-ping Lin, Jie Wang, Peng-lian Du, Wan-liang Liu, Li Lin, Jin-xi Wang, Yi-long Wang, Yong-jun Liu, Gai-fen Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke |
title | Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke |
title_full | Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke |
title_fullStr | Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke |
title_full_unstemmed | Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke |
title_short | Phosphodiesterase 4D polymorphisms associate with the short-term outcome in ischemic stroke |
title_sort | phosphodiesterase 4d polymorphisms associate with the short-term outcome in ischemic stroke |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320494/ https://www.ncbi.nlm.nih.gov/pubmed/28225001 http://dx.doi.org/10.1038/srep42914 |
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