Clinical Evaluation of Cerebrospinal Fluid p217tau and Neurofilament Light Chain Levels in Patients with Alzheimer’s Disease or Other Neurological Diseases

Author:

Kawarabayashi Takeshi123,Nakamura Takumi23,Miyashita Kazuya4,Segawa Tatsuya4,Fukamachi Isamu4,Sugawara Takashi1,Oka Hironori1,Ishizawa Kunihiko1,Amari Masakuni1,Kasahara Hiroo2,Makioka Kouki2,Ikeda Yoshio2,Takatama Masamitsu1,Shoji Mikio123

Affiliation:

1. Department of Neurology, Dementia Research Center, Geriatrics Research Institute and Hospital, Maebashi, Japan

2. Department of Neurology, Gunma University Hospital, Maebashi, Japan

3. Department of Social Medicine, Hirosaki University Graduate School of Medicine, Hirosaki, Japan

4. Immuno-Biological Laboratories Co., Ltd, Fujioka, Japan

Abstract

Background: The cerebrospinal fluid (CSF) levels of tau phosphorylated at threonine 217 (p217tau) or 181 (p181tau), and neurofilament light chain (NfL) are definite biomarkers of tauopathy and neurodegeneration in Alzheimer’s disease (AD). Objective: To validate their utility in excluding other neurological diseases and age-related changes in clinical settings. Methods: We developed monoclonal antibodies against p217tau and NfL, established novel ELISAs, and analyzed 170 CSF samples from patients with AD or other neurological diseases. Results: In AD, p217tau is a more specific and abundant CSF component than p181tau. However, CSF NfL levels increase age-dependently and to a greater extent in central and peripheral nervous diseases than in AD. Conclusions: CSF p217tau correlates better with AD neurodegeneration than other tau-related biomarkers and the major phosphorylated tau species. The clinical usage of NfL as a neurodegeneration biomarker in AD requires exclusion of various central and peripheral neurological diseases.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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