Friederike Schulze, Juhani Määttä, Sybille Grad, Irina Heggli, Florian Brunner, Mazda Farshad, Oliver Distler, Jaro Karppinen, Jeffrey Lotz, Stefan Dudli
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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":"7 3","pages":""},"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":"{\"title\":\"Proteomic analysis of serum in a population-based cohort did not reveal a biomarker for Modic changes\",\"authors\":\"Friederike Schulze, Juhani Määttä, Sybille Grad, Irina Heggli, Florian Brunner, Mazda Farshad, Oliver Distler, Jaro Karppinen, Jeffrey Lotz, 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. 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引用次数: 0
摘要
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。
Proteomic analysis of serum in a population-based cohort did not reveal a biomarker for Modic changes
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.