帕金森病中 PGLYRP2 变异 rs892145 的等位基因分布的性别差异

IF 2.1 4区 医学 Q3 CLINICAL NEUROLOGY Parkinson's Disease Pub Date : 2023-12-09 DOI:10.1155/2023/6502727
Caroline Ran, Karin Wirdefeldt, Olof Sydow, Per Svenningsson, Rochellys Diaz Heijtz
{"title":"帕金森病中 PGLYRP2 变异 rs892145 的等位基因分布的性别差异","authors":"Caroline Ran, Karin Wirdefeldt, Olof Sydow, Per Svenningsson, Rochellys Diaz Heijtz","doi":"10.1155/2023/6502727","DOIUrl":null,"url":null,"abstract":"<i>Introduction</i>. Parkinson’s disease (PD) is a complex multifactorial disease, involving genetic susceptibility, environmental risk factors, and gene-environmental interactions. The microbiota-gut-brain axis is hypothesized to play a role in the pathophysiology of PD, and peptidoglycan recognition proteins (PGLYRPs), which modulate the gut microbiota, are, therefore, relevant candidate genes for PD. <i>Methods</i>. Using quantitative real-time PCR, we genotyped three <i>PGLYRP</i> variants (rs892145, rs959117, and rs10888557) and performed an association analysis in 508 PD patients and 585 control individuals. We further conducted a meta-analysis of rs892145 and analyzed <i>PGLYRP2</i> gene expression in lymphocytes from patients with PD and controls. <i>Results</i>. Although initial analysis of the three variants rs892145, rs959117, and rs10888557 and a meta-analysis of rs892145 did not reveal any association between the selected variants and PD, we found an interaction between sex and genotype for rs892145, with a marked difference in the allele distribution of rs892145 between male and female patients. As compared to controls, the T allele was less common in female patients (odds ratio = 0.76, <svg height=\"8.68572pt\" style=\"vertical-align:-0.0498209pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.6359 8.15071 8.68572\" width=\"8.15071pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"></path></g></svg> = 0.04) and more common in male patients (odds ratio = 1.29, <svg height=\"8.68572pt\" style=\"vertical-align:-0.0498209pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.6359 8.15071 8.68572\" width=\"8.15071pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"><use xlink:href=\"#g113-81\"></use></g></svg> = 0.04). No difference was found in <i>PGLYRP2</i> gene expression between PD patients and controls (<svg height=\"8.68572pt\" style=\"vertical-align:-0.0498209pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.6359 8.15071 8.68572\" width=\"8.15071pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"><use xlink:href=\"#g113-81\"></use></g></svg> = 0.38), nor between sexes (<svg height=\"8.68572pt\" style=\"vertical-align:-0.0498209pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.6359 8.15071 8.68572\" width=\"8.15071pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"><g transform=\"matrix(.013,0,0,-0.013,0,0)\"><use xlink:href=\"#g113-81\"></use></g></svg> = 0.07). <i>Discussion</i>. Overall, this genetic screening in Swedish PD patients does not support previous results demonstrating associations of <i>PGLYRP</i> variants with the risk of PD. Meta-analysis of rs892145 revealed pronounced heterogeneity between previously published studies which is likely to have influenced the results. Taken together, the genetic and gene expression analyses suggest a possible link between genetic variants in <i>PGLYRP2</i> and sex differences in PD. Because of the limited sample size in our study, these results need to be verified in independent cohorts before concluding.","PeriodicalId":19907,"journal":{"name":"Parkinson's Disease","volume":"9 1","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2023-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sex Differences in the Allele Distribution of PGLYRP2 Variant rs892145 in Parkinson’s Disease\",\"authors\":\"Caroline Ran, Karin Wirdefeldt, Olof Sydow, Per Svenningsson, Rochellys Diaz Heijtz\",\"doi\":\"10.1155/2023/6502727\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<i>Introduction</i>. Parkinson’s disease (PD) is a complex multifactorial disease, involving genetic susceptibility, environmental risk factors, and gene-environmental interactions. The microbiota-gut-brain axis is hypothesized to play a role in the pathophysiology of PD, and peptidoglycan recognition proteins (PGLYRPs), which modulate the gut microbiota, are, therefore, relevant candidate genes for PD. <i>Methods</i>. Using quantitative real-time PCR, we genotyped three <i>PGLYRP</i> variants (rs892145, rs959117, and rs10888557) and performed an association analysis in 508 PD patients and 585 control individuals. We further conducted a meta-analysis of rs892145 and analyzed <i>PGLYRP2</i> gene expression in lymphocytes from patients with PD and controls. <i>Results</i>. Although initial analysis of the three variants rs892145, rs959117, and rs10888557 and a meta-analysis of rs892145 did not reveal any association between the selected variants and PD, we found an interaction between sex and genotype for rs892145, with a marked difference in the allele distribution of rs892145 between male and female patients. As compared to controls, the T allele was less common in female patients (odds ratio = 0.76, <svg height=\\\"8.68572pt\\\" style=\\\"vertical-align:-0.0498209pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.6359 8.15071 8.68572\\\" width=\\\"8.15071pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"></path></g></svg> = 0.04) and more common in male patients (odds ratio = 1.29, <svg height=\\\"8.68572pt\\\" style=\\\"vertical-align:-0.0498209pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.6359 8.15071 8.68572\\\" width=\\\"8.15071pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"><use xlink:href=\\\"#g113-81\\\"></use></g></svg> = 0.04). No difference was found in <i>PGLYRP2</i> gene expression between PD patients and controls (<svg height=\\\"8.68572pt\\\" style=\\\"vertical-align:-0.0498209pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.6359 8.15071 8.68572\\\" width=\\\"8.15071pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"><use xlink:href=\\\"#g113-81\\\"></use></g></svg> = 0.38), nor between sexes (<svg height=\\\"8.68572pt\\\" style=\\\"vertical-align:-0.0498209pt\\\" version=\\\"1.1\\\" viewbox=\\\"-0.0498162 -8.6359 8.15071 8.68572\\\" width=\\\"8.15071pt\\\" xmlns=\\\"http://www.w3.org/2000/svg\\\" xmlns:xlink=\\\"http://www.w3.org/1999/xlink\\\"><g transform=\\\"matrix(.013,0,0,-0.013,0,0)\\\"><use xlink:href=\\\"#g113-81\\\"></use></g></svg> = 0.07). <i>Discussion</i>. Overall, this genetic screening in Swedish PD patients does not support previous results demonstrating associations of <i>PGLYRP</i> variants with the risk of PD. Meta-analysis of rs892145 revealed pronounced heterogeneity between previously published studies which is likely to have influenced the results. Taken together, the genetic and gene expression analyses suggest a possible link between genetic variants in <i>PGLYRP2</i> and sex differences in PD. Because of the limited sample size in our study, these results need to be verified in independent cohorts before concluding.\",\"PeriodicalId\":19907,\"journal\":{\"name\":\"Parkinson's Disease\",\"volume\":\"9 1\",\"pages\":\"\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2023-12-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Parkinson's Disease\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1155/2023/6502727\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Parkinson's Disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/2023/6502727","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

简介:帕金森病(PD)是一种复杂的多因素疾病。帕金森病(PD)是一种复杂的多因素疾病,涉及遗传易感性、环境风险因素以及基因与环境的相互作用。据推测,微生物群-肠道-大脑轴在帕金森病的病理生理学中发挥作用,而肽聚糖识别蛋白(PGLYRPs)能调节肠道微生物群,因此是帕金森病的相关候选基因。研究方法利用定量实时 PCR 技术,我们对三个 PGLYRP 变体(rs892145、rs959117 和 rs10888557)进行了基因分型,并对 508 名 PD 患者和 585 名对照者进行了关联分析。我们进一步对 rs892145 进行了荟萃分析,并分析了 PGLYRP2 基因在 PD 患者和对照组淋巴细胞中的表达。结果。尽管对三个变异体rs892145、rs959117和rs10888557的初步分析以及对rs892145的荟萃分析并未发现所选变异体与帕金森病之间存在任何关联,但我们发现rs892145的性别与基因型之间存在交互作用,男性和女性患者之间的rs892145等位基因分布存在明显差异。与对照组相比,T等位基因在女性患者中较少见(几率比=0.76,=0.04),而在男性患者中较常见(几率比=1.29,=0.04)。在PGLYRP2基因表达方面,帕金森病患者与对照组(= 0.38)和性别间(= 0.07)均无差异。讨论总体而言,此次对瑞典帕金森病患者进行的基因筛查并不支持之前证明 PGLYRP 变异与帕金森病风险相关的结果。对 rs892145 进行的元分析表明,以前发表的研究之间存在明显的异质性,这很可能影响了研究结果。综上所述,遗传和基因表达分析表明,PGLYRP2的遗传变异与帕金森病的性别差异之间可能存在联系。由于我们的研究样本量有限,这些结果需要在独立队列中验证后才能得出结论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Sex Differences in the Allele Distribution of PGLYRP2 Variant rs892145 in Parkinson’s Disease
Introduction. Parkinson’s disease (PD) is a complex multifactorial disease, involving genetic susceptibility, environmental risk factors, and gene-environmental interactions. The microbiota-gut-brain axis is hypothesized to play a role in the pathophysiology of PD, and peptidoglycan recognition proteins (PGLYRPs), which modulate the gut microbiota, are, therefore, relevant candidate genes for PD. Methods. Using quantitative real-time PCR, we genotyped three PGLYRP variants (rs892145, rs959117, and rs10888557) and performed an association analysis in 508 PD patients and 585 control individuals. We further conducted a meta-analysis of rs892145 and analyzed PGLYRP2 gene expression in lymphocytes from patients with PD and controls. Results. Although initial analysis of the three variants rs892145, rs959117, and rs10888557 and a meta-analysis of rs892145 did not reveal any association between the selected variants and PD, we found an interaction between sex and genotype for rs892145, with a marked difference in the allele distribution of rs892145 between male and female patients. As compared to controls, the T allele was less common in female patients (odds ratio = 0.76,  = 0.04) and more common in male patients (odds ratio = 1.29,  = 0.04). No difference was found in PGLYRP2 gene expression between PD patients and controls ( = 0.38), nor between sexes ( = 0.07). Discussion. Overall, this genetic screening in Swedish PD patients does not support previous results demonstrating associations of PGLYRP variants with the risk of PD. Meta-analysis of rs892145 revealed pronounced heterogeneity between previously published studies which is likely to have influenced the results. Taken together, the genetic and gene expression analyses suggest a possible link between genetic variants in PGLYRP2 and sex differences in PD. Because of the limited sample size in our study, these results need to be verified in independent cohorts before concluding.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Parkinson's Disease
Parkinson's Disease CLINICAL NEUROLOGY-
CiteScore
5.80
自引率
3.10%
发文量
0
审稿时长
18 weeks
期刊介绍: Parkinson’s Disease is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies related to the epidemiology, etiology, pathogenesis, genetics, cellular, molecular and neurophysiology, as well as the diagnosis and treatment of Parkinson’s disease.
期刊最新文献
Effectiveness and Feasibility of Nonpharmacological Interventions for People With Parkinson's Disease and Cognitive Impairment on Patient-Centred Outcomes: Systematic Review and Meta-Analysis. Validation and Psychometric Properties of the Spanish Version of King's Parkinson's Disease Pain Scale. A Cognitive-Behavioral Model of Apathy in Parkinson's Disease. Possible Implications of Managing Alexithymia on Quality of Life in Parkinson's Disease: A Systematic Review. Implications of Convolutional Neural Network for Brain MRI Image Classification to Identify Alzheimer's Disease.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1