Salivary α-Synuclein as a Candidate Biomarker of Parkinsonism in 22q11.2 Deletion Syndrome.

M. Fanella, Emanuele Cerulli Irelli, T. Accinni, F. Di Fabio, Carolina Putotto, Federica Pulvirenti, Francesco E Bellomi, C. Di Bonaventura, Giorgio Vivacqua
{"title":"Salivary α-Synuclein as a Candidate Biomarker of Parkinsonism in 22q11.2 Deletion Syndrome.","authors":"M. Fanella, Emanuele Cerulli Irelli, T. Accinni, F. Di Fabio, Carolina Putotto, Federica Pulvirenti, Francesco E Bellomi, C. Di Bonaventura, Giorgio Vivacqua","doi":"10.1002/mdc3.14046","DOIUrl":null,"url":null,"abstract":"BACKGROUND\n22q11.2 deletion syndrome (22q11.2DS) has been linked to an increased risk of early-onset Parkinson's disease. However, the pathophysiological mechanisms underlying parkinsonism remain poorly understood.\n\n\nOBJECTIVE\nThe objective is to investigate salivary total α-synuclein levels in 22q11.2DS patients with and without parkinsonian motor signs.\n\n\nMETHODS\nThis cross-sectional study included 10 patients with 22q11.2DS with parkinsonism (Park+), ten 22q11.2DS patients without parkinsonism (Park-), and 10 age and sex-comparable healthy subjects (HS). Salivary and serum α-synuclein levels were measured using enzyme-linked immunosorbent assay.\n\n\nRESULTS\nSalivary total α-synuclein concentration was significantly lower in Park (+) patients than in Park (-) patients and HS (P = 0.007). In addition, salivary α-synuclein showed good accuracy in discriminating Park (+) from Park (-) patients (area under the curve = 0.86) and correlated with motor severity and cognitive impairment.\n\n\nCONCLUSION\nThis exploratory study suggests that the parkinsonian phenotype of 22q11.2DS is associated with a reduced concentration of monomeric α-synuclein in biological fluids.","PeriodicalId":509823,"journal":{"name":"Movement Disorders Clinical Practice","volume":"11 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Movement Disorders Clinical Practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/mdc3.14046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND 22q11.2 deletion syndrome (22q11.2DS) has been linked to an increased risk of early-onset Parkinson's disease. However, the pathophysiological mechanisms underlying parkinsonism remain poorly understood. OBJECTIVE The objective is to investigate salivary total α-synuclein levels in 22q11.2DS patients with and without parkinsonian motor signs. METHODS This cross-sectional study included 10 patients with 22q11.2DS with parkinsonism (Park+), ten 22q11.2DS patients without parkinsonism (Park-), and 10 age and sex-comparable healthy subjects (HS). Salivary and serum α-synuclein levels were measured using enzyme-linked immunosorbent assay. RESULTS Salivary total α-synuclein concentration was significantly lower in Park (+) patients than in Park (-) patients and HS (P = 0.007). In addition, salivary α-synuclein showed good accuracy in discriminating Park (+) from Park (-) patients (area under the curve = 0.86) and correlated with motor severity and cognitive impairment. CONCLUSION This exploratory study suggests that the parkinsonian phenotype of 22q11.2DS is associated with a reduced concentration of monomeric α-synuclein in biological fluids.
唾液中的α-突触核蛋白是22q11.2缺失综合征帕金森病的候选生物标记物
背景22q11.2缺失综合征(22q11.2DS)与早发帕金森病的风险增加有关。方法这项横断面研究纳入了 10 名伴有帕金森病的 22q11.2DS 患者(Park+)、10 名不伴有帕金森病的 22q11.2DS 患者(Park-)以及 10 名年龄和性别相当的健康受试者(HS)。结果Park(+)患者唾液总α-突触核蛋白浓度明显低于Park(-)患者和HS(P = 0.007)。此外,唾液中的α-突触核蛋白在区分帕金森(+)和帕金森(-)患者方面显示出良好的准确性(曲线下面积 = 0.86),并与运动严重程度和认知障碍相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信