已发表论文

PLA2G6  遗传变异和帕金森氏病之间缺乏联系:系统回顾

 

Authors Liu H, Yao Y, Liu H, Peng Y, Ren J, Wu X, Mao R, Zhao J, Zhu Y, Niu Z, Yang T, Sun X, Jiang P, Zhang C, Fang Y

Received 15 March 2020

Accepted for publication 6 June 2020

Published 23 July 2020 Volume 2020:16 Pages 1755—1763

DOI https://doi.org/10.2147/NDT.S254065

Checked for plagiarism Yes

Review by Single-blind

Peer reviewer comments 2

Editor who approved publication: Professor Jun Chen

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.
Keywords: Parkinson’s disease, PD, PLA2G6 , systematic review




Figure 1 Flow diagram of the study selection process.