Prognostic value of neurofilament light chain in natalizumab therapy for different phases of multiple sclerosis: A systematic review and meta-analysis

纳塔利祖玛 医学 多发性硬化 神经丝 荟萃分析 生物标志物 内科学 视神经脊髓炎 神经退行性变 肿瘤科 疾病 免疫学 免疫组织化学 生物化学 化学
作者
Ning Liu,Mengjiao Sun,Wenjing Zhang,Jing Sun,Panpan Gong,Hongxia Wang,Manxia Wang
出处
期刊:Journal of Clinical Neuroscience [Elsevier BV]
卷期号:101: 198-203 被引量:4
标识
DOI:10.1016/j.jocn.2022.04.041
摘要

A systematic review and meta-analysis of the prognostic value of neurofilament light chain levels in multiple sclerosis treatment with natalizumab Relevant studies published before January 2022 were retrieved from the PubMed, Web of Science, and clinicaltrials.gov databases. Qualitative analysis and meta-analysis were included in 7 of the 46 papers. Differences in the Neurofilament light chain levels were used as the main efficacy measures, and the meta-analysis was performed using Review Manager version 5.3 software. Seven clinical trials were selected. Neurofilament light chain levels were lower in the 947 patients on natalizumab treatment than the 959 patients before therapy, with a moderate effect size of 0.73 (p < 0.00001). Mean Neurofilament light chain levels showed no significant difference between the remitting and relapsing phase of MS before and after natalizumab treatment. The EDSS scores of 41 MS patients in the relapsing phase after natalizumab treatment were significantly lower than those in 102 MS patients without therapy (MD = -0.45;95% CI = -0.85 to -0.05;P < 0.001). However, the EDSS scores in the remitting phase demonstrated no difference. The comparison of Neurofilament light chain across multiple groups demonstrates the potential of Nfl as a noninvasive biomarker of neurodegeneration, evaluating the efficacy of natalizumab in MS patients. We also investigated the relationship between different phases of relapsing-remitting MS with Neurofilament light chain levels. However, the value of Neurofilament light chain as a biomarker was hard to assess due to the limited number of studies. For clinical application, a comprehensive understanding of Neurofilament light chain concentrations in disease subtypes is required, and disease stages should be defined to develop standardized criteria.

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