Department of Neurology, University Hospital Frankfurt, Frankfurt am Main 60590, Germany.
Department of Neurology, University Hospital Frankfurt, Frankfurt am Main 60590, Germany.
Mult Scler Relat Disord. 2022 Jul;63:103822. doi: 10.1016/j.msard.2022.103822. Epub 2022 Apr 23.
Cognitive performance may be impaired in MS even at the earliest stages of disease. We tested whether brain-derived neurotrophic factor and neurofilament light chain levels in serum and cerebrospinal fluid (CSF) samples (sNfL/cNfL/sBDNF/cBDNF) collected at the time of diagnosis are associated with cognitive performance.
We measured sNfL/cNfL/sBDNF/cBDNF using single-molecule array (Simoa) in 47 newly diagnosed patients (32 relapsing-remitting MS/6 primary progressive MS/9 clinically isolated syndrome). Partial correlations between average z-score on neuropsychological tests and sNfL/sBDNF/cNfL/cBDNF were computed after adjusting for covariates. Multivariate analysis of covariance determined the effect of cognitive status on biomarker levels. A composite measure of NfL and BDNF was submitted to similar exploratory analysis.
Cognitive performance correlated inversely with cNfL (r=-0.451/q=0.032) and cBDNF (r=-0.406/q=0.034). Impairment in at least two different tests was linked to higher cNfL (p=0.011) and cBDNF (p=0.035) levels compared to impairment in only one test and for cNfL also compared to no impairment at all (p=0.01). Composite CSF biomarker measure accounting for both cNfL and cBDNF correlated more strongly with tests of information processing (p=0.048) and verbal learning/memory consolidation (p = 0.02) as compared to the single CSF biomarkers.
CSF BDNF and NfL levels measured at the time of diagnosis are inversely associated with cognitive performance in MS. Our findings suggest that CSF biomarkers linked to different pathophysiological processes reflect neuropsychological impairment in the earliest stages of the disease. Combining different CSF measures might facilitate the developing of a better biomarker of cognition in MS.
即使在疾病的早期阶段,多发性硬化症(MS)也可能导致认知表现受损。我们检测了在诊断时采集的血清和脑脊液(CSF)样本(sNfL/cNfL/sBDNF/cBDNF)中的脑源性神经营养因子和神经丝轻链水平是否与认知表现相关。
我们使用单分子阵列(Simoa)在 47 名新诊断的患者(32 名复发缓解型 MS/6 名原发性进展型 MS/9 名临床孤立综合征)中测量了 sNfL/cNfL/sBDNF/cBDNF。在调整协变量后,计算神经心理学测试的平均 z 评分与 sNfL/sBDNF/cNfL/cBDNF 之间的部分相关性。协方差的多变量分析确定了认知状态对生物标志物水平的影响。将 NfL 和 BDNF 的组合测量值提交给类似的探索性分析。
认知表现与 cNfL(r=-0.451/q=0.032)和 cBDNF(r=-0.406/q=0.034)呈负相关。与仅一项测试受损相比,至少两项不同测试受损与更高的 cNfL(p=0.011)和 cBDNF(p=0.035)水平相关,而与所有测试均未受损相比,cNfL 也具有更高的水平(p=0.01)。考虑到 cNfL 和 cBDNF 的复合 CSF 生物标志物测量与信息处理(p=0.048)和言语学习/记忆巩固(p=0.02)的测试相关性更强,与单个 CSF 生物标志物相比。
在诊断时测量的 CSF BDNF 和 NfL 水平与 MS 患者的认知表现呈负相关。我们的研究结果表明,与不同病理生理过程相关的 CSF 生物标志物反映了疾病早期的神经心理学损伤。结合不同的 CSF 测量可能有助于更好地开发 MS 认知的生物标志物。