Glial Fibrillary Acidic Protein's Usefulness as an Astrocyte Biomarker Using the Fully Automated LUMIPULSE® System.

IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Jo Kamada, Tomohiro Hamanaka, Aya Oshimo, Hideo Sato, Tomonori Nishii, Marika Fujita, Yoshiharu Makiguchi, Miki Tanaka, Katsumi Aoyagi, Hisashi Nojima
{"title":"Glial Fibrillary Acidic Protein's Usefulness as an Astrocyte Biomarker Using the Fully Automated LUMIPULSE<sup>®</sup> System.","authors":"Jo Kamada, Tomohiro Hamanaka, Aya Oshimo, Hideo Sato, Tomonori Nishii, Marika Fujita, Yoshiharu Makiguchi, Miki Tanaka, Katsumi Aoyagi, Hisashi Nojima","doi":"10.3390/diagnostics14222520","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Glial fibrillary acidic protein (GFAP) is an important biomarker for neuroinflammatory conditions. Recently, advancements in the treatment of neurological diseases have highlighted the increasing importance of biomarkers, creating a demand for accurate and simple measurement systems for GFAP levels, which are essential for both research and clinical applications. This study presents the development and validation of a novel fully automated immunoassay for the quantitative determination of GFAP levels in biological samples.</p><p><strong>Methods: </strong>We examined the analytical performance of the GFAP assay on the LUMIPULSE platform. The assay's parameters, including antibody concentrations, incubation times, and detection methods, were optimized to enhance sensitivity and specificity. GFAP levels were measured in 396 serum or plasma samples, comprising both healthy controls and patients with neurodegenerative diseases.</p><p><strong>Results: </strong>In the analytical performance studies, intra- and inter-assay coefficients of variation (CV) were below 5%, indicating high reproducibility. Additionally, the assay demonstrated good linearity over the measurement range. The limit of quantification (LoQ) for this assay was 6.0 pg/mL, which is sufficient for measuring specimens from healthy controls. In clinical validation studies, GFAP levels were significantly elevated in patients with neurodegenerative diseases compared to healthy controls.</p><p><strong>Conclusions: </strong>This automated GFAP assay provides a robust and reliable tool for GFAP measurement, facilitating further research into GFAP's role in neurological disorders and potentially aiding in the diagnosis and monitoring of these conditions.</p>","PeriodicalId":11225,"journal":{"name":"Diagnostics","volume":"14 22","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diagnostics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/diagnostics14222520","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Glial fibrillary acidic protein (GFAP) is an important biomarker for neuroinflammatory conditions. Recently, advancements in the treatment of neurological diseases have highlighted the increasing importance of biomarkers, creating a demand for accurate and simple measurement systems for GFAP levels, which are essential for both research and clinical applications. This study presents the development and validation of a novel fully automated immunoassay for the quantitative determination of GFAP levels in biological samples.

Methods: We examined the analytical performance of the GFAP assay on the LUMIPULSE platform. The assay's parameters, including antibody concentrations, incubation times, and detection methods, were optimized to enhance sensitivity and specificity. GFAP levels were measured in 396 serum or plasma samples, comprising both healthy controls and patients with neurodegenerative diseases.

Results: In the analytical performance studies, intra- and inter-assay coefficients of variation (CV) were below 5%, indicating high reproducibility. Additionally, the assay demonstrated good linearity over the measurement range. The limit of quantification (LoQ) for this assay was 6.0 pg/mL, which is sufficient for measuring specimens from healthy controls. In clinical validation studies, GFAP levels were significantly elevated in patients with neurodegenerative diseases compared to healthy controls.

Conclusions: This automated GFAP assay provides a robust and reliable tool for GFAP measurement, facilitating further research into GFAP's role in neurological disorders and potentially aiding in the diagnosis and monitoring of these conditions.

使用全自动 LUMIPULSE® 系统分析胶质纤维酸性蛋白作为星形胶质细胞生物标记物的有用性
背景:胶质纤维酸性蛋白(GFAP)是神经炎症的重要生物标志物。近来,神经系统疾病治疗的进步凸显了生物标志物日益增长的重要性,从而产生了对准确、简便的 GFAP 水平测量系统的需求,这对研究和临床应用都至关重要。本研究开发并验证了一种新型全自动免疫测定法,用于定量测定生物样本中的 GFAP 水平:我们在 LUMIPULSE 平台上检验了 GFAP 分析法的分析性能。我们优化了测定参数,包括抗体浓度、孵育时间和检测方法,以提高灵敏度和特异性。对 396 份血清或血浆样本(包括健康对照组和神经退行性疾病患者)中的 GFAP 水平进行了测定:在分析性能研究中,测定内和测定间的变异系数(CV)均低于 5%,表明重现性很高。此外,该检测方法在测量范围内表现出良好的线性。该测定的定量限(LoQ)为 6.0 pg/mL,足以测量健康对照组的标本。在临床验证研究中,与健康对照组相比,神经退行性疾病患者的 GFAP 水平明显升高:这种自动 GFAP 检测方法为 GFAP 的测量提供了一种稳健可靠的工具,有助于进一步研究 GFAP 在神经系统疾病中的作用,并有可能帮助诊断和监测这些疾病。
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
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
×
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