Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy

Background: The association between inflammation and neurodegeneration has long been observed in parkinson’s disease (PD) and multiple system atrophy (MSA). Previous genome-wide association studies (GWAS) and meta-analyses have identified several risk loci in inflammation-associated genes associated...

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Autores principales: Wei-Ming Su, Xiao-Jing Gu, Yan-Bing Hou, Ling-Yu Zhang, Bei Cao, Ru-Wei Ou, Ying Wu, Xue-Ping Chen, Wei Song, Bi Zhao, Hui-Fang Shang, Yong-Ping Chen
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:4769c9cc41c445d7bc226fded8a1cedf2021-11-18T05:51:59ZAssociation Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy1664-802110.3389/fgene.2021.765833https://doaj.org/article/4769c9cc41c445d7bc226fded8a1cedf2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fgene.2021.765833/fullhttps://doaj.org/toc/1664-8021Background: The association between inflammation and neurodegeneration has long been observed in parkinson’s disease (PD) and multiple system atrophy (MSA). Previous genome-wide association studies (GWAS) and meta-analyses have identified several risk loci in inflammation-associated genes associated with PD.Objective: To investigate whether polymorphisms in some inflammation-associated genes could modulate the risk of developing PD and MSA in a Southwest Chinese population.Methods: A total of 2,706 Chinese subjects comprising 1340 PD, 483 MSA and 883 healthy controls were recruited in the study. Three polymorphisms (rs2074404 GG/GT/TT, rs17425622 CC/CT/TT, rs34043159 CC/CT/TT) in genes linked to inflammation in all the subjects were genotyped by using the Sequenom iPLEX Assay.Results: The allele G of WNT3 rs2074404 can increase risk on PD (OR: 1.048, 95% CI: 1.182–1.333, p = 0.006), exclusively in the LOPD subgroup (OR: 1.166, 95% CI:1.025–1.327, p = 0.019), but not in EOPD or MSA. And the recessive model analysis also demonstrated an increased PD risk in GG genotype of this locus (OR = 1.331, p = 0.007). However, no significant differences were observed in the genotype distributions and alleles of HLA-DRB5 rs17425622 and IL1R2 rs34043159 between the PD patients and controls, between the MSA patients and controls, or between subgroups of PD or MSA and controls.Conclusion: Our results suggested the allele G of WNT3 rs2074404 have an adverse effect on PD and particularly, on the LOPD subgroup among a Chinese population.Wei-Ming SuWei-Ming SuWei-Ming SuXiao-Jing GuXiao-Jing GuXiao-Jing GuYan-Bing HouYan-Bing HouYan-Bing HouLing-Yu ZhangLing-Yu ZhangLing-Yu ZhangBei CaoBei CaoBei CaoRu-Wei OuRu-Wei OuRu-Wei OuYing WuYing WuYing WuXue-Ping ChenXue-Ping ChenXue-Ping ChenWei SongWei SongWei SongBi ZhaoBi ZhaoBi ZhaoHui-Fang ShangHui-Fang ShangHui-Fang ShangYong-Ping ChenYong-Ping ChenYong-Ping ChenFrontiers Media S.A.articleparkinsion’s diseasemultiple system atrophyWnt3HLA-DRB5IL1R2SNPGeneticsQH426-470ENFrontiers in Genetics, Vol 12 (2021)
institution DOAJ
collection DOAJ
language EN
topic parkinsion’s disease
multiple system atrophy
Wnt3
HLA-DRB5
IL1R2
SNP
Genetics
QH426-470
spellingShingle parkinsion’s disease
multiple system atrophy
Wnt3
HLA-DRB5
IL1R2
SNP
Genetics
QH426-470
Wei-Ming Su
Wei-Ming Su
Wei-Ming Su
Xiao-Jing Gu
Xiao-Jing Gu
Xiao-Jing Gu
Yan-Bing Hou
Yan-Bing Hou
Yan-Bing Hou
Ling-Yu Zhang
Ling-Yu Zhang
Ling-Yu Zhang
Bei Cao
Bei Cao
Bei Cao
Ru-Wei Ou
Ru-Wei Ou
Ru-Wei Ou
Ying Wu
Ying Wu
Ying Wu
Xue-Ping Chen
Xue-Ping Chen
Xue-Ping Chen
Wei Song
Wei Song
Wei Song
Bi Zhao
Bi Zhao
Bi Zhao
Hui-Fang Shang
Hui-Fang Shang
Hui-Fang Shang
Yong-Ping Chen
Yong-Ping Chen
Yong-Ping Chen
Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
description Background: The association between inflammation and neurodegeneration has long been observed in parkinson’s disease (PD) and multiple system atrophy (MSA). Previous genome-wide association studies (GWAS) and meta-analyses have identified several risk loci in inflammation-associated genes associated with PD.Objective: To investigate whether polymorphisms in some inflammation-associated genes could modulate the risk of developing PD and MSA in a Southwest Chinese population.Methods: A total of 2,706 Chinese subjects comprising 1340 PD, 483 MSA and 883 healthy controls were recruited in the study. Three polymorphisms (rs2074404 GG/GT/TT, rs17425622 CC/CT/TT, rs34043159 CC/CT/TT) in genes linked to inflammation in all the subjects were genotyped by using the Sequenom iPLEX Assay.Results: The allele G of WNT3 rs2074404 can increase risk on PD (OR: 1.048, 95% CI: 1.182–1.333, p = 0.006), exclusively in the LOPD subgroup (OR: 1.166, 95% CI:1.025–1.327, p = 0.019), but not in EOPD or MSA. And the recessive model analysis also demonstrated an increased PD risk in GG genotype of this locus (OR = 1.331, p = 0.007). However, no significant differences were observed in the genotype distributions and alleles of HLA-DRB5 rs17425622 and IL1R2 rs34043159 between the PD patients and controls, between the MSA patients and controls, or between subgroups of PD or MSA and controls.Conclusion: Our results suggested the allele G of WNT3 rs2074404 have an adverse effect on PD and particularly, on the LOPD subgroup among a Chinese population.
format article
author Wei-Ming Su
Wei-Ming Su
Wei-Ming Su
Xiao-Jing Gu
Xiao-Jing Gu
Xiao-Jing Gu
Yan-Bing Hou
Yan-Bing Hou
Yan-Bing Hou
Ling-Yu Zhang
Ling-Yu Zhang
Ling-Yu Zhang
Bei Cao
Bei Cao
Bei Cao
Ru-Wei Ou
Ru-Wei Ou
Ru-Wei Ou
Ying Wu
Ying Wu
Ying Wu
Xue-Ping Chen
Xue-Ping Chen
Xue-Ping Chen
Wei Song
Wei Song
Wei Song
Bi Zhao
Bi Zhao
Bi Zhao
Hui-Fang Shang
Hui-Fang Shang
Hui-Fang Shang
Yong-Ping Chen
Yong-Ping Chen
Yong-Ping Chen
author_facet Wei-Ming Su
Wei-Ming Su
Wei-Ming Su
Xiao-Jing Gu
Xiao-Jing Gu
Xiao-Jing Gu
Yan-Bing Hou
Yan-Bing Hou
Yan-Bing Hou
Ling-Yu Zhang
Ling-Yu Zhang
Ling-Yu Zhang
Bei Cao
Bei Cao
Bei Cao
Ru-Wei Ou
Ru-Wei Ou
Ru-Wei Ou
Ying Wu
Ying Wu
Ying Wu
Xue-Ping Chen
Xue-Ping Chen
Xue-Ping Chen
Wei Song
Wei Song
Wei Song
Bi Zhao
Bi Zhao
Bi Zhao
Hui-Fang Shang
Hui-Fang Shang
Hui-Fang Shang
Yong-Ping Chen
Yong-Ping Chen
Yong-Ping Chen
author_sort Wei-Ming Su
title Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
title_short Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
title_full Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
title_fullStr Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
title_full_unstemmed Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson’s Disease and Multiple System Atrophy
title_sort association analysis of wnt3, hla-drb5 and il1r2 polymorphisms in chinese patients with parkinson’s disease and multiple system atrophy
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/4769c9cc41c445d7bc226fded8a1cedf
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