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进行性多发性硬化症中的神经丝:系统评价。

Neurofilaments in progressive multiple sclerosis: a systematic review.

机构信息

Department of Neuroinflammation, Faculty of Brain Sciences, Queen Square Multiple Sclerosis Centre, UCL Queen Square Institute of Neurology, University College London, London, UK.

Department of Neurodegenerative Disease, Faculty of Brain Sciences, UCL Queen Square Institute of Neurology, University College London, London, UK.

出版信息

J Neurol. 2021 Sep;268(9):3212-3222. doi: 10.1007/s00415-020-09917-x. Epub 2020 May 23.

Abstract

BACKGROUND

Neurofilament proteins have been extensively studied in relapsing-remitting multiple sclerosis, where they are promising biomarkers of disease activity and treatment response. Their role in progressive multiple sclerosis, where there is a particularly urgent need for improved biomarkers, is less clear. The objectives of this systematic review are to summarise the literature on neurofilament light and heavy in progressive multiple sclerosis, addressing key questions.

METHODS

A systematic search of PubMed, Embase, Web of Science and Scopus identified 355 potential sources. 76 relevant sources were qualitatively reviewed using QUADAS-2 criteria, and 17 were identified as at low risk of bias. We summarise the findings from all relevant sources, and separately from the 17 high-quality studies.

RESULTS

Differences in neurofilament light between relapsing-remitting and progressive multiple sclerosis appear to be explained by differences in covariates. Neurofilament light is consistently associated with current inflammatory activity and future brain atrophy in progressive multiple sclerosis, and is consistently shown to be a marker of treatment response with immunosuppressive disease-modifying therapies. Associations with current or future disability are inconsistent, and there is no evidence of NFL being a responsive marker of purportedly neuroprotective treatments. Evidence on neurofilament heavy is more limited and inconsistent.

CONCLUSIONS

Neurofilament light has shown consistent utility as a biomarker of neuroinflammation, future brain atrophy and immunosuppressive treatment response at a group level. Neither neurofilament light or heavy has shown a consistent treatment response to neuroprotective disease-modifying therapies, which will require further data from successful randomised controlled trials.

摘要

背景

神经丝蛋白在复发缓解型多发性硬化症中得到了广泛研究,它们是疾病活动和治疗反应的有前途的生物标志物。它们在进展型多发性硬化症中的作用不太清楚,而进展型多发性硬化症尤其需要改进的生物标志物。本系统综述的目的是总结神经丝轻链和重链在进展型多发性硬化症中的文献,以解决关键问题。

方法

通过对 PubMed、Embase、Web of Science 和 Scopus 的系统搜索,确定了 355 个潜在来源。使用 QUADAS-2 标准对 76 个相关来源进行了定性审查,并确定了 17 个低偏倚风险的来源。我们总结了所有相关来源的发现,并分别总结了 17 个高质量研究的发现。

结果

复发缓解型和进展型多发性硬化症之间神经丝轻链的差异似乎可以用协变量的差异来解释。神经丝轻链与进展型多发性硬化症中的当前炎症活动和未来脑萎缩始终相关,并且与免疫抑制性疾病修正治疗的治疗反应始终相关,被证明是一种标志物。与当前或未来残疾的相关性不一致,并且没有证据表明 NFL 是神经保护治疗的反应性标志物。神经丝重链的证据更有限且不一致。

结论

神经丝轻链在群体水平上作为神经炎症、未来脑萎缩和免疫抑制治疗反应的生物标志物显示出一致的效用。神经丝轻链和重链均未显示出对神经保护疾病修正治疗的一致治疗反应,这将需要从成功的随机对照试验中获得更多数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26d3/8357650/65be3d87b7b8/415_2020_9917_Fig1_HTML.jpg

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