Porter Lachlan, Shoushtarizadeh Alireza, Jelinek George A, Brown Chelsea R, Lim Chai K, de Livera Alysha M, Jacobs Kelly R, Weiland Tracey J
Neuroepidemiology Unit, Melbourne School of Population and Global Health, The University of Melbourne, Carlton, VIC, Australia.
The Peter Doherty Institute for Infection and Immunity, Melbourne, VIC, Australia.
Front Mol Biosci. 2020 Dec 14;7:574133. doi: 10.3389/fmolb.2020.574133. eCollection 2020.
Magnetic resonance imaging (MRI), cerebrospinal fluid (CSF) analysis, and the McDonald's clinical criteria are currently utilized tools in diagnosing multiple sclerosis. However, a more conclusive, consistent, and efficient way of diagnosing multiple sclerosis (MS) is yet to be discovered. A potential biomarker, discovered using advances in high-throughput sequencing such as nuclear magnetic resonance (NMR) spectroscopy and other "Omics"-based techniques, may make diagnosis and prognosis more reliable resulting in a more personalized and targeted treatment regime and improved outcomes. The aim of this review was to systematically search the literature for potential biomarkers from any bodily fluid that could consistently and accurately diagnose MS and/or indicate disease progression.
A systematic literature review of EMBASE, PubMed (MEDLINE), The Cochrane Library, and CINAHL databases produced over a thousand potential studies. Inclusion criteria stated studies with potential biomarker outcomes for people with MS were to be included in the review. Studies were limited to those with human participants who had a clinically defined diagnosis of MS and published in English, with no limit placed on date of publication or the type of bodily fluid sampled.
A total of 1,805 studies were recorded from the literature search. A total of 1,760 studies were removed based on their abstract, with a further 18 removed after considering the full text. A total of 30 studies were considered relevant and had their data retrieved and analyzed. Due to the heterogeneity of focus and results from the refined studies, a narrative synthesis was favored.
Several promising candidate biomarkers suitable for clinical application in MS have been studied. It is recommended follow-up studies with larger sample sizes be completed on several potential biomarkers.
磁共振成像(MRI)、脑脊液(CSF)分析以及麦克唐纳临床标准是目前用于诊断多发性硬化症的工具。然而,尚未发现一种更具决定性、一致性和高效性的诊断多发性硬化症(MS)的方法。利用高通量测序技术(如核磁共振(NMR)光谱)和其他基于“组学”的技术所发现的潜在生物标志物,可能会使诊断和预后更可靠,从而形成更个性化、有针对性的治疗方案并改善治疗效果。本综述的目的是系统检索文献,寻找可用于持续、准确诊断MS和/或指示疾病进展的来自任何体液的潜在生物标志物。
对EMBASE、PubMed(MEDLINE)、Cochrane图书馆和CINAHL数据库进行系统文献综述,产生了一千多项潜在研究。纳入标准规定,具有MS患者潜在生物标志物结果的研究应纳入本综述。研究限于有临床明确诊断为MS的人类参与者且以英文发表的研究,对发表日期或所采集体液类型不设限制。
从文献检索中总共记录了1805项研究。根据摘要共排除1760项研究,在考虑全文后又排除18项。总共30项研究被认为相关,并检索和分析了它们的数据。由于精细研究的重点和结果存在异质性,故采用叙述性综合分析。
已经对几种有望用于MS临床应用的候选生物标志物进行了研究。建议对几种潜在生物标志物开展更大样本量的后续研究。