神经丝轻链改善格林-巴-罗综合征的临床预后模型。

IF 8.7 1区 医学 Q1 CLINICAL NEUROLOGY
Robin C M Thomma, Linda W G Luijten, Sander J van Tilburg, Eveline J A Wiegers, Charlotte E Teunissen, Lisa Vermunt, Pieter A van Doorn, Ruth Huizinga, Bart C Jacobs
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引用次数: 0

摘要

背景:几种预测格林-巴- 综合征(GBS)临床结局的预后模型。近年来,神经丝轻链(neurofilament light chain, NfL)已成为一种预测预后的生物标志物。我们研究了血清(sNfL)和脑脊液(cNfL)中NfL对基于临床因素预测GBS患者呼吸衰竭和无法行走的模型的附加预后价值。方法:我们纳入了来自随机安慰剂对照试验的患者(GBS患者第二次静脉注射免疫球蛋白)。入园时和入园第1、2、4、12周采集血清,入园时采集脑脊液。通过单分子阵列测定NfL水平。采用logistic回归分析评估NfL对(改良的)Erasmus GBS结局评分(m)EGOS)和(改良的)Erasmus GBS呼吸功能不全评分的附加预后价值。结果:共纳入293例患者(74例(25%)机械通气,38/275例(13%)26周时不能行走)。入院时、第1周和第2周较高的sNfL和入院时的cNfL与4周和26周时无法行走有关。入组时sNfL和cNfL水平均与呼吸衰竭无关。添加NfL后EGOS和mEGOS均有改善(∆c -统计范围:0.01-0.11),尤其是预测26周预后的模型。预测26周时无法行走的新模型由入组时sNfL、入组时GBS残疾评分和第2周时医学研究委员会总评分组成,效果最佳(c统计量:0.88 (95% CI 0.83至0.94))。结论:NfL的加入可以改善临床预后模型对行走能力的预测,但不能改善呼吸衰竭的预测。试验注册号:NTR2224/NL2107。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurofilament light chain improves clinical prognostic models for Guillain-Barré syndrome.

Background: Several prognostic models predict clinical outcomes in Guillain-Barré syndrome (GBS). Recently, neurofilament light chain (NfL) has emerged as a prognostic biomarker. We investigated the added prognostic value of NfL in serum (sNfL) and cerebrospinal fluid (cNfL) to models based on clinical factors predicting respiratory failure and inability to walk in GBS.

Methods: We included patients from a randomised placebo-controlled trial (second intravenous immunoglobulin dose in GBS). Serum was acquired at entry and week 1, 2, 4 and 12 and cerebrospinal fluid at entry. NfL levels were determined on a single molecule array. The additional prognostic value of NfL to the (modified) Erasmus GBS Outcome Score ((m)EGOS) and (modified) Erasmus GBS Respiratory Insufficiency Score was evaluated using logistic regression analyses.

Results: In total, 293 patients were included (74 (25%) mechanically ventilated, 38/275 (13%) unable to walk at 26 weeks). Higher sNfL at entry, week 1 and week 2 and cNfL at entry were associated with inability to walk at 4 and 26 weeks. Neither sNfL nor cNfL levels at entry were associated with respiratory failure. The EGOS and mEGOS improved after adding NfL (∆C-statistic range: 0.01-0.11), especially the models predicting outcome at 26 weeks. A new model predicting inability to walk at 26 weeks consisting of sNfL at entry, GBS disability score at entry and Medical Research Council sum score at week 2 performed best (C-statistic: 0.88 (95% CI 0.83 to 0.94)).

Conclusions: Addition of NfL may improve clinical prognostic models for the prediction of inability to walk, but not of respiratory failure.

Trial registration number: NTR2224/NL2107.

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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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