Drebrin is a novel biomarker of cognitive deterioration in Alzheimer's disease

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Authors: Mikio Shoji, Takeshi Kawarabayashi, Takumi Nakamura, Takashi Sugawara, Kunihiko Ishizawa, Masakuni Amari, Ryoma Takahashi, Hiroo Kasahara, Noriko Koganezawa, Ayaka Higa, Masamitsu Takatama, Yoshio Ikeda
+2 more Yuko Sekino, Tomoaki Shirao
Cited by: 1
References: 49

Abstract

ratio, p-217tau and p-181tau, and neurofilament light chain are biomarkers of Aβ proteinopathy, tau proteinopathy, and neuronal injury, respectively, in Alzheimer's disease (AD). However, direct biomarkers of cognitive function have yet to be identified.ObjectiveTherefore, the present study investigated the potential of CSF and plasma levels of drebrin, a postsynaptic protein, as biomarkers of synaptic activity and cognitive function in the human brain in clinical settings.MethodsWe developed a novel ELISA to measure CSF and plasma levels of drebrin and analyzed 68 CSF and 128 plasma samples from patients with AD and other neurological diseases.ResultsCSF drebrin levels were significantly reduced in samples of mild cognitive impairment due to AD, the dementia stages of AD, and idiopathic normal pressure hydrocephalus. Plasma drebrin levels were also significantly reduced in samples of MCI due to AD.ConclusionsCSF and plasma drebrin levels are specific biomarkers of cognitive decline in the MCI stage of AD.

Fields of Study & Subjects

Cerebrospinal fluid and hydrocephalus Alzheimer's disease research and treatments Dementia and Cognitive Impairment Research

Publication details

Journal / source
Journal of Alzheimer s Disease
Publisher
SAGE Publications
Volume
109
Issue
4
Pages
1824–1833
Publication date
2 January 2026
Language
EN