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Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk
Several studies have investigated a potential association between the endothelial lipase gene (LIPG) 584C/T polymorphism and susceptibility to coronary artery disease (CAD), but a uniform conclusion is yet to be reached. To better evaluate the true relationship between the LIPG 584C/T polymorphism a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494996/ https://www.ncbi.nlm.nih.gov/pubmed/32893849 http://dx.doi.org/10.1042/BSR20200027 |
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author | Wu, Yue-e Ma, Lan Zhang, Hao Chen, Xin-ran Xu, Xin-yi Hu, Ze-ping |
author_facet | Wu, Yue-e Ma, Lan Zhang, Hao Chen, Xin-ran Xu, Xin-yi Hu, Ze-ping |
author_sort | Wu, Yue-e |
collection | PubMed |
description | Several studies have investigated a potential association between the endothelial lipase gene (LIPG) 584C/T polymorphism and susceptibility to coronary artery disease (CAD), but a uniform conclusion is yet to be reached. To better evaluate the true relationship between the LIPG 584C/T polymorphism and the risk of CAD, a meta-analysis of 14 case–control studies with 9731 subjects was performed. Relevant articles published through August 2020 were searched in the CNKI, PubMed, Embase and Web of Science databases. Thirteen articles, including 14 eligible case–control studies with 4025 cases and 5706 controls, were enrolled in the present meta-analysis. The Newcastle–Ottawa Scale (NOS) scores of the case–control studies ranged from 6 to 8. The pooled results indicated that there is a significant association between the LIPG 584C/T polymorphism and CAD in the homozygote comparison model and the allelic comparison model. Subgroup analyses revealed that the LIPG 584C/T mutation significantly decreased the risk of CAD in the subgroups of African, CAD, hospital-based (HB), and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) populations in some genetic models. No publication bias was found in our meta-analysis, which certifies the robustness of the current meta-analysis. Trial sequential analysis (TSA) also confirmed the stability of our results. The results of our meta-analysis indicate that the LIPG 584C/T polymorphism plays a protective role in the incidence of CAD. More high-quality case–control studies on various ethnicities are needed to confirm our results. |
format | Online Article Text |
id | pubmed-7494996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74949962020-09-24 Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk Wu, Yue-e Ma, Lan Zhang, Hao Chen, Xin-ran Xu, Xin-yi Hu, Ze-ping Biosci Rep Diagnostics & Biomarkers Several studies have investigated a potential association between the endothelial lipase gene (LIPG) 584C/T polymorphism and susceptibility to coronary artery disease (CAD), but a uniform conclusion is yet to be reached. To better evaluate the true relationship between the LIPG 584C/T polymorphism and the risk of CAD, a meta-analysis of 14 case–control studies with 9731 subjects was performed. Relevant articles published through August 2020 were searched in the CNKI, PubMed, Embase and Web of Science databases. Thirteen articles, including 14 eligible case–control studies with 4025 cases and 5706 controls, were enrolled in the present meta-analysis. The Newcastle–Ottawa Scale (NOS) scores of the case–control studies ranged from 6 to 8. The pooled results indicated that there is a significant association between the LIPG 584C/T polymorphism and CAD in the homozygote comparison model and the allelic comparison model. Subgroup analyses revealed that the LIPG 584C/T mutation significantly decreased the risk of CAD in the subgroups of African, CAD, hospital-based (HB), and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) populations in some genetic models. No publication bias was found in our meta-analysis, which certifies the robustness of the current meta-analysis. Trial sequential analysis (TSA) also confirmed the stability of our results. The results of our meta-analysis indicate that the LIPG 584C/T polymorphism plays a protective role in the incidence of CAD. More high-quality case–control studies on various ethnicities are needed to confirm our results. Portland Press Ltd. 2020-09-16 /pmc/articles/PMC7494996/ /pubmed/32893849 http://dx.doi.org/10.1042/BSR20200027 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). |
spellingShingle | Diagnostics & Biomarkers Wu, Yue-e Ma, Lan Zhang, Hao Chen, Xin-ran Xu, Xin-yi Hu, Ze-ping Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk |
title | Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk |
title_full | Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk |
title_fullStr | Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk |
title_full_unstemmed | Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk |
title_short | Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk |
title_sort | significant association between the endothelial lipase gene 584c/t polymorphism and coronary artery disease risk |
topic | Diagnostics & Biomarkers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494996/ https://www.ncbi.nlm.nih.gov/pubmed/32893849 http://dx.doi.org/10.1042/BSR20200027 |
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