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Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review

BACKGROUND: The phospholipase A2 Group 6 (PLA2G6, also known as PLA2, PARK14, and iPLA2) gene encodes a group VIA calcium-independent phospholipase A2. Genetic polymorphism of PLA2G6 has been indicated to be involved in conferring susceptibility for Parkinson’s disease (PD), whereas conclusive resul...

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Autores principales: Liu, Hongmei, Yao, Yamin, Liu, Hongbo, Peng, Yanmin, Ren, Juanjuan, Wu, Xiaohui, Mao, Ruizhi, Zhao, Jie, Zhu, Yuncheng, Niu, Zhiang, Yang, Tao, Sun, Xiujia, Jiang, Ping, Zhang, Chen, Fang, Yiru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399463/
https://www.ncbi.nlm.nih.gov/pubmed/32801710
http://dx.doi.org/10.2147/NDT.S254065
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author Liu, Hongmei
Yao, Yamin
Liu, Hongbo
Peng, Yanmin
Ren, Juanjuan
Wu, Xiaohui
Mao, Ruizhi
Zhao, Jie
Zhu, Yuncheng
Niu, Zhiang
Yang, Tao
Sun, Xiujia
Jiang, Ping
Zhang, Chen
Fang, Yiru
author_facet Liu, Hongmei
Yao, Yamin
Liu, Hongbo
Peng, Yanmin
Ren, Juanjuan
Wu, Xiaohui
Mao, Ruizhi
Zhao, Jie
Zhu, Yuncheng
Niu, Zhiang
Yang, Tao
Sun, Xiujia
Jiang, Ping
Zhang, Chen
Fang, Yiru
author_sort Liu, Hongmei
collection PubMed
description BACKGROUND: The phospholipase A2 Group 6 (PLA2G6, also known as PLA2, PARK14, and iPLA2) gene encodes a group VIA calcium-independent phospholipase A2. Genetic polymorphism of PLA2G6 has been indicated to be involved in conferring susceptibility for Parkinson’s disease (PD), whereas conclusive results have not been obtained. Thus, we intended to conduct a systematic review to determine if PLA2G6 genetic variation confers a greater susceptibility to PD. METHODS: All case-control studies that investigated the association of the PLA2G6 polymorphisms with the risk of PD published before 15 July 2018 were included. The literature was comprehensively searched and identified in five English databases (EBSCO, Pubmed, OVID, EMBASE and ISI Web of Knowledge) and four Chinese databases (Wanfang database, Chinese Biomedical Literature Database, China Academic Journals Database and VIP database). We performed analyses of study characteristics, heterogeneity, and forest plot in analyses analogous to dominant, codominant and additive models with the pooled odds ratio (OR) in fixed- or random-effects models as the measure of association. RESULTS: A total of 664 potentially relevant studies were retrieved with the initial search, of which eight studies fulfilled the inclusion criteria, and included 2,779 PD patients and 3,291 control participants,. Among all the reported 27 genetic variants, 15 single nucleotide polymorphisms (SNPs) were present only in patients, and only five available SNPs (rs2267369, rs140758033, c.1959T>A (Gly653Gly), rs76718524, rs199935023) were pooled in the meta-analysis. However, there was no evidence for a significant association between the five SNPs and PD risk in dominant, codominant and allele models, suggesting a lack of association between PLA2G6 genetic variation and PD susceptibility. CONCLUSION: The present study assessed the association of PLA2G6 genetic polymorphism with the risk PD, and the result strongly demonstrates that PLA2G6 polymorphism is not associated with PD susceptibility.
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spelling pubmed-73994632020-08-14 Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review Liu, Hongmei Yao, Yamin Liu, Hongbo Peng, Yanmin Ren, Juanjuan Wu, Xiaohui Mao, Ruizhi Zhao, Jie Zhu, Yuncheng Niu, Zhiang Yang, Tao Sun, Xiujia Jiang, Ping Zhang, Chen Fang, Yiru Neuropsychiatr Dis Treat Original Research BACKGROUND: The phospholipase A2 Group 6 (PLA2G6, also known as PLA2, PARK14, and iPLA2) gene encodes a group VIA calcium-independent phospholipase A2. Genetic polymorphism of PLA2G6 has been indicated to be involved in conferring susceptibility for Parkinson’s disease (PD), whereas conclusive results have not been obtained. Thus, we intended to conduct a systematic review to determine if PLA2G6 genetic variation confers a greater susceptibility to PD. METHODS: All case-control studies that investigated the association of the PLA2G6 polymorphisms with the risk of PD published before 15 July 2018 were included. The literature was comprehensively searched and identified in five English databases (EBSCO, Pubmed, OVID, EMBASE and ISI Web of Knowledge) and four Chinese databases (Wanfang database, Chinese Biomedical Literature Database, China Academic Journals Database and VIP database). We performed analyses of study characteristics, heterogeneity, and forest plot in analyses analogous to dominant, codominant and additive models with the pooled odds ratio (OR) in fixed- or random-effects models as the measure of association. RESULTS: A total of 664 potentially relevant studies were retrieved with the initial search, of which eight studies fulfilled the inclusion criteria, and included 2,779 PD patients and 3,291 control participants,. Among all the reported 27 genetic variants, 15 single nucleotide polymorphisms (SNPs) were present only in patients, and only five available SNPs (rs2267369, rs140758033, c.1959T>A (Gly653Gly), rs76718524, rs199935023) were pooled in the meta-analysis. However, there was no evidence for a significant association between the five SNPs and PD risk in dominant, codominant and allele models, suggesting a lack of association between PLA2G6 genetic variation and PD susceptibility. CONCLUSION: The present study assessed the association of PLA2G6 genetic polymorphism with the risk PD, and the result strongly demonstrates that PLA2G6 polymorphism is not associated with PD susceptibility. Dove 2020-07-23 /pmc/articles/PMC7399463/ /pubmed/32801710 http://dx.doi.org/10.2147/NDT.S254065 Text en © 2020 Liu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Liu, Hongmei
Yao, Yamin
Liu, Hongbo
Peng, Yanmin
Ren, Juanjuan
Wu, Xiaohui
Mao, Ruizhi
Zhao, Jie
Zhu, Yuncheng
Niu, Zhiang
Yang, Tao
Sun, Xiujia
Jiang, Ping
Zhang, Chen
Fang, Yiru
Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review
title Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review
title_full Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review
title_fullStr Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review
title_full_unstemmed Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review
title_short Lack of Association Between PLA2G6 Genetic Variation and Parkinson’s Disease: A Systematic Review
title_sort lack of association between pla2g6 genetic variation and parkinson’s disease: a systematic review
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399463/
https://www.ncbi.nlm.nih.gov/pubmed/32801710
http://dx.doi.org/10.2147/NDT.S254065
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