Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia

被引:355
作者
Rohrer, Jonathan D. [1 ]
Woollacott, Ione O. C. [1 ]
Dick, Katrina M. [1 ]
Brotherhood, Emilie [1 ]
Gordon, Elizabeth [1 ]
Fellows, Alexander [1 ]
Toombs, Jamie [3 ,4 ]
Druyeh, Ronald [2 ]
Cardoso, M. Jorge [1 ]
Ourselin, Sebastien [1 ,5 ]
Nicholas, Jennifer M. [1 ,5 ,6 ]
Norgren, Niklas [7 ]
Mead, Simon [2 ]
Andreasson, Ulf [8 ]
Blennow, Kaj [8 ]
Schott, Jonathan M. [1 ]
Fox, Nick C. [1 ]
Warren, Jason D. [1 ]
Zetterberg, Henrik [3 ,4 ,8 ]
机构
[1] UCL Inst Neurol, Dementia Res Ctr, Queen Sq, London, England
[2] UCL Inst Neurol, MRC Prion Unit, Queen Sq, London, England
[3] UCL Inst Neurol, Dept Neurodegenerat Dis, Queen Sq, London, England
[4] UCL Inst Neurol, Dept Mol Neurosci, Queen Sq, London, England
[5] UCL, Ctr Med Image Comp, London WC1E 6BT, England
[6] London Sch Hyg & Trop Med, Dept Med Stat, London, England
[7] UmanDiagnostics, Umea, Sweden
[8] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Clin Neurochem Lab,Dept Psychiat & Neurochem, Molndal, Sweden
基金
英国医学研究理事会; 瑞典研究理事会;
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; ALZHEIMERS-DISEASE; CSF; DEGENERATION; DIAGNOSIS; SEGMENTATION; PROGRESSION; BIOMARKERS; SEVERITY; CRITERIA;
D O I
10.1212/WNL.0000000000003154
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective:To investigate serum neurofilament light chain (NfL) concentrations in frontotemporal dementia (FTD) and to see whether they are associated with the severity of disease.Methods:Serum samples were collected from 74 participants (34 with behavioral variant FTD [bvFTD], 3 with FTD and motor neuron disease and 37 with primary progressive aphasia [PPA]) and 28 healthy controls. Twenty-four of the FTD participants carried a pathogenic mutation in C9orf72 (9), microtubule-associated protein tau (MAPT; 11), or progranulin (GRN; 4). Serum NfL concentrations were determined with the NF-Light kit transferred onto the single-molecule array platform and compared between FTD and healthy controls and between the FTD clinical and genetic subtypes. We also assessed the relationship between NfL concentrations and measures of cognition and brain volume.Results:Serum NfL concentrations were higher in patients with FTD overall (mean 77.9 pg/mL [SD 51.3 pg/mL]) than controls (19.6 pg/mL [SD 8.2 pg/mL]; p < 0.001). Concentrations were also significantly higher in bvFTD (57.8 pg/mL [SD 33.1 pg/mL]) and both the semantic and nonfluent variants of PPA (95.9 and 82.5 pg/mL [SD 33.0 and 33.8 pg/mL], respectively) compared with controls and in semantic variant PPA compared with logopenic variant PPA. Concentrations were significantly higher than controls in both the C9orf72 and MAPT subgroups (79.2 and 40.5 pg/mL [SD 48.2 and 20.9 pg/mL], respectively) with a trend to a higher level in the GRN subgroup (138.5 pg/mL [SD 103.3 pg/mL). However, there was variability within all groups. Serum concentrations correlated particularly with frontal lobe atrophy rate (r = 0.53, p = 0.003).Conclusions:Increased serum NfL concentrations are seen in FTD but show wide variability within each clinical and genetic group. Higher concentrations may reflect the intensity of the disease in FTD and are associated with more rapid atrophy of the frontal lobes.
引用
收藏
页码:1329 / 1336
页数:8
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