Proteomic analysis of serum in a population-based cohort did not reveal a biomarker for Modic changes

IF 3.4 3区 医学 Q1 ORTHOPEDICS
JOR Spine Pub Date : 2024-07-15 DOI:10.1002/jsp2.1337
Friederike Schulze, Juhani Määttä, Sybille Grad, Irina Heggli, Florian Brunner, Mazda Farshad, Oliver Distler, Jaro Karppinen, Jeffrey Lotz, Stefan Dudli
{"title":"Proteomic analysis of serum in a population-based cohort did not reveal a biomarker for Modic changes","authors":"Friederike Schulze,&nbsp;Juhani Määttä,&nbsp;Sybille Grad,&nbsp;Irina Heggli,&nbsp;Florian Brunner,&nbsp;Mazda Farshad,&nbsp;Oliver Distler,&nbsp;Jaro Karppinen,&nbsp;Jeffrey Lotz,&nbsp;Stefan Dudli","doi":"10.1002/jsp2.1337","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Introduction</h3>\n \n <p>Modic changes (MC) are bone marrow lesions of vertebral bones, which can be detected with magnetic resonance imaging (MRI) adjacent to degenerated intervertebral discs. Defined by their appearance on T1 and T2 weighted images, there are three interconvertible types: MC1, MC2, and MC3. The inter-observer variability of the MRI diagnosis is high, therefore a diagnostic serum biomarker complementing the MRI to facilitate diagnosis and follow-up would be of great value.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We used a highly sensitive and reproducible proteomics approach: DIA/SWATH-MS to find serum biomarkers in a subset of the Northern Finland Birth Cohort 1966. Separately, we measured a panel of factors involved in inflammation and angiogenesis to confirm some potential biomarkers published before with an ELISA-based method called V-Plex.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>We found neither an association between the serum concentrations of the proteins detected with DIA/SWATH-MS with the presence of MC, nor a correlation with the size of the MC lesions. We did not find any association between the factors measured with the V-Plex and the presence of MC or their size.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Altogether, our study suggests that a robust and generally usable biomarker to facilitate the diagnosis of MC cannot readily be found in serum.</p>\n </section>\n </div>","PeriodicalId":14876,"journal":{"name":"JOR Spine","volume":null,"pages":null},"PeriodicalIF":3.4000,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11250394/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JOR Spine","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jsp2.1337","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Modic changes (MC) are bone marrow lesions of vertebral bones, which can be detected with magnetic resonance imaging (MRI) adjacent to degenerated intervertebral discs. Defined by their appearance on T1 and T2 weighted images, there are three interconvertible types: MC1, MC2, and MC3. The inter-observer variability of the MRI diagnosis is high, therefore a diagnostic serum biomarker complementing the MRI to facilitate diagnosis and follow-up would be of great value.

Methods

We used a highly sensitive and reproducible proteomics approach: DIA/SWATH-MS to find serum biomarkers in a subset of the Northern Finland Birth Cohort 1966. Separately, we measured a panel of factors involved in inflammation and angiogenesis to confirm some potential biomarkers published before with an ELISA-based method called V-Plex.

Results

We found neither an association between the serum concentrations of the proteins detected with DIA/SWATH-MS with the presence of MC, nor a correlation with the size of the MC lesions. We did not find any association between the factors measured with the V-Plex and the presence of MC or their size.

Conclusion

Altogether, our study suggests that a robust and generally usable biomarker to facilitate the diagnosis of MC cannot readily be found in serum.

Abstract Image

对基于人群的队列中的血清进行蛋白质组学分析,并未发现 Modic 变化的生物标志物。
简介莫迪氏病变(MC)是脊椎骨的骨髓病变,可通过磁共振成像(MRI)在退化的椎间盘附近发现。根据其在 T1 和 T2 加权图像上的表现,可定义为三种可相互转换的类型:MC1、MC2 和 MC3。核磁共振成像诊断的观察者间变异性很高,因此,诊断性血清生物标志物与核磁共振成像相辅相成,有助于诊断和随访,具有重要价值:方法:我们采用了一种高灵敏度和可重复性的蛋白质组学方法:DIA/SWATH-MS方法,在1966年北芬兰出生队列的一个子集中寻找血清生物标志物。另外,我们还测量了一组涉及炎症和血管生成的因子,以确认之前用一种名为 V-Plex 的 ELISA 方法公布的一些潜在生物标志物:结果:我们发现,DIA/SWATH-MS 检测到的蛋白质的血清浓度与 MC 的存在之间没有关联,与 MC 病变的大小也没有关联。我们也没有发现用 V-Plex 检测到的因素与 MC 的存在或其大小有任何关联:总之,我们的研究表明,在血清中无法轻易找到一种可靠且普遍可用的生物标志物来帮助诊断 MC。
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
JOR Spine
JOR Spine ORTHOPEDICS-
CiteScore
6.40
自引率
18.90%
发文量
42
审稿时长
10 weeks
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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