Advances in biomarkers in multiple system atrophy.

IF 3.9 3区 医学 Q1 PATHOLOGY
Anastasia Bougea
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引用次数: 0

Abstract

Introduction: In order to improve illness identification, monitoring, and patient outcomes, this special report emphasizes the revolutionary potential of fluid and imaging biomarkers using new diagnostic technologies in Multiple system atrophy (MSA).

Areas covered: Innovations like multiplex seeding aggregation assays (SAA), 18FDG-Positron Emission Tomography (PET), and SPECT) are changing the diagnostic landscape. These techniques make it easier to detect MSA early and offer noninvasive monitoring choices. Although neurofilament light chain measurements in blood and cerebrospinal fluid (CSF), as well as α-synuclein-based diagnostic biomarkers in CSF, are recognized as both diagnostic and surrogatemarkers of disease progression in MSA, their application in clinical practiceis limited to research. Some efforts are being made in the development ofselective α- synucleinPET tracers despite numerous barriers in visualizing intracellular localization of α-synuclein. The primary drawbacks include the high expense of SAA and imaging technologies, the paucity of multicenter longitudinal investigations, and the lack of uniformity of the prοtocols. The research highlights that to successfully solve these restrictions, stakeholders must continue to collaborate.

Expert opinion: A multi-dimensional biomarker system of MSA patients maximizes the power of contemporary diagnostics to enhance MSA care by prioritizing the ongoing evaluation of multi-omics data.

多系统萎缩生物标志物研究进展。
为了改善疾病的识别、监测和患者的预后,本特别报告强调了在多系统萎缩(MSA)中使用新的诊断技术的液体和成像生物标志物的革命性潜力。涵盖领域:诸如多重种子聚集测定(SAA), 18fdg -正电子发射断层扫描(PET)和spect等创新正在改变诊断领域。这些技术使早期发现MSA更容易,并提供非侵入性监测选择。尽管血液和脑脊液(CSF)中的神经丝轻链测量以及CSF中基于α-突触核蛋白的诊断生物标志物被认为是MSA疾病进展的诊断和替代标志物,但它们在临床实践中的应用仅限于研究。尽管在观察α-突触核蛋白的细胞内定位方面存在许多障碍,但人们仍在努力开发选择性α-突触核蛋白pet示踪剂。主要的缺点包括高费用的SAA和成像技术,缺乏多中心纵向调查,以及缺乏统一的医疗工具。研究强调,要成功解决这些限制,利益相关者必须继续合作。专家意见:MSA患者的多维生物标志物系统通过优先考虑正在进行的多组学数据评估,最大限度地提高当代诊断的能力,以加强MSA护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
71
审稿时长
1 months
期刊介绍: Expert Review of Molecular Diagnostics (ISSN 1473-7159) publishes expert reviews of the latest advancements in the field of molecular diagnostics including the detection and monitoring of the molecular causes of disease that are being translated into groundbreaking diagnostic and prognostic technologies to be used in the clinical diagnostic setting. Each issue of Expert Review of Molecular Diagnostics contains leading reviews on current and emerging topics relating to molecular diagnostics, subject to a rigorous peer review process; editorials discussing contentious issues in the field; diagnostic profiles featuring independent, expert evaluations of diagnostic tests; meeting reports of recent molecular diagnostics conferences and key paper evaluations featuring assessments of significant, recently published articles from specialists in molecular diagnostic therapy. Expert Review of Molecular Diagnostics provides the forum for reporting the critical advances being made in this ever-expanding field, as well as the major challenges ahead in their clinical implementation. The journal delivers this information in concise, at-a-glance article formats: invaluable to a time-constrained community.
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