Demographic and disease-related factors impact on cerebrospinal fluid neurofilament light chain levels in multiple sclerosis

被引:1
作者
Revendova, Kamila Zondra [1 ,2 ,3 ]
Cucuzza, Chiara Starvaggi [1 ,2 ]
Manouchehrinia, Ali [1 ]
Khademi, Mohsen [1 ]
Bar, Michal [3 ]
Leppert, David [4 ,5 ]
Sandberg, Elisabeth [6 ]
Ouellette, Russell [6 ]
Granberg, Tobias [6 ]
Piehl, Fredrik [1 ,2 ]
机构
[1] Karolinska Inst, Ctr Mol Med, Dept Clin Neurosci, Stockholm, Sweden
[2] Karolinska Univ Hosp, Acad Specialist Ctr, Ctr Neurol, Stockholm, Sweden
[3] Univ Ostrava, Fac Med, Dept Clin Neurosci, Ostrava, Czech Republic
[4] Neurol Clin & Policlin, MS Ctr, Basel, Switzerland
[5] Res Ctr Clin Neuroimmunol & Neurosci Basel RC2NB, Basel, Switzerland
[6] Karolinska Univ Hosp, Dept Neuroradiol, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
biomarker; multiple sclerosis; neurofilament light chain; progressive multiple sclerosis; relapsing-remitting multiple sclerosis; disease-modifying therapies; brain atrophy; BIOMARKER;
D O I
10.1002/brb3.2873
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
BackgroundNeurofilament light (NfL) levels reflect inflammatory disease activity in multiple sclerosis (MS), but it is less clear if NfL also can serve as a biomarker for MS progression in treated patients without relapses and focal lesion accrual. In addition, it has not been well established if clinically effective treatment re-establishes an age and sex pattern for cerebrospinal fluid NfL (cNfL) as seen in controls, and to what degree levels are affected by disability level and magnetic resonance imaging (MRI) atrophy metrics. MethodsWe included subjects for whom cNfL levels had been determined as per clinical routine or in clinical research, classified as healthy controls (HCs, n = 89), MS-free disease controls (DCs, n = 251), untreated MS patients (uMS; n = 296), relapse-free treated MS patients (tMS; n = 78), and ProTEct-MS clinical trial participants (pMS; n = 41). ResultsUsing linear regression, we found a positive association between cNfL and age, as well as lower concentrations among women, in all groups, except for uMS patients. In contrast, disability level in the entire MS cohort, or T1 and T2 lesion volumes, brain parenchymal fraction, thalamic fraction, and cortical thickness in the pMS trial cohort, did not correlate with cNfL concentrations. Furthermore, the cNfL levels in tMS and pMS groups did not differ. ConclusionsIn participants with MS lacking signs of inflammatory disease activity, disease modulatory therapy reinstates an age and sex cNfL pattern similar to that of control subjects. No significant association was found between cNfL levels and clinical worsening, disability level, or MRI metrics.
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