Association of Plasma Claudin-5 with Age and Alzheimer Disease.

Alzheimer disease biomarker blood–brain barrier claudin-5 dementia tight junction

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
24 Jan 2024
Historique:
received: 01 01 2024
revised: 17 01 2024
accepted: 19 01 2024
medline: 10 2 2024
pubmed: 10 2 2024
entrez: 10 2 2024
Statut: epublish

Résumé

The blood-brain barrier (BBB) plays pivotal roles in synaptic and neuronal functioning by sealing the space between adjacent microvascular endothelial cells. BBB breakdown is present in patients with mild cognitive impairment (MCI) or Alzheimer disease (AD). Claudin-5 (CLDN-5) is a tetra-spanning protein essential for sealing the intercellular space between adjacent endothelial cells in the BBB. In this study, we developed a blood-based assay for CLDN-5 and investigated its diagnostic utility using 100 cognitively normal (control) subjects, 100 patients with MCI, and 100 patients with AD. Plasma CLDN-5 levels were increased in patients with AD (3.08 ng/mL) compared with controls (2.77 ng/mL). Plasma levels of phosphorylated tau (pTau181), a biomarker of pathological tau, were elevated in patients with MCI or AD (2.86 and 4.20 pg/mL, respectively) compared with control subjects (1.81 pg/mL). In patients with MCI or AD, plasma levels of CLDN-5-but not pTau181-decreased with age, suggesting some age-dependent BBB changes in MCI and AD. These findings suggest that plasma CLDN-5 may a potential biochemical marker for the diagnosis of AD.

Identifiants

pubmed: 38338697
pii: ijms25031419
doi: 10.3390/ijms25031419
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Japan Agency for Medical Research and Development
ID : JP20hm0102084
Organisme : Japan Society for the Promotion of Science
ID : 21H03354, 22H03953, 22K19936

Auteurs

Keisuke Tachibana (K)

Graduate School of Pharmaceutical Sciences, Osaka University, Suita 565-0871, Osaka, Japan.

Ryuichi Hirayama (R)

Graduate School of Medicine, Osaka University, Suita 565-0871, Osaka, Japan.

Naoyuki Sato (N)

Graduate School of Medicine, Osaka University, Suita 565-0871, Osaka, Japan.
Department of Aging Neurobiology, Center for Development of Advanced Medicine for Dementia, National Center for Geriatrics and Gerontology, Obu 474-8511, Aichi, Japan.

Kotaro Hattori (K)

Department of Bioresources, Medical Genome Center, National Center of Neurology and Psychiatry, Kodaira 187-8551, Tokyo, Japan.

Takashi Kato (T)

Department of Clinical and Experimental Neuroimaging, National Center for Geriatrics and Gerontology, Obu 474-8511, Aichi, Japan.

Hiroyuki Takeda (H)

Proteo-Science Center, Ehime University, Matsuyama 790-8577, Ehime, Japan.

Masuo Kondoh (M)

Graduate School of Pharmaceutical Sciences, Osaka University, Suita 565-0871, Osaka, Japan.

Classifications MeSH