Neural cell adhesion molecule 1 is a cellular target engaged plasma biomarker in demyelinating Charcot-Marie-Tooth disease.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
06 2023
Historique:
revised: 03 02 2023
received: 08 09 2022
accepted: 22 02 2023
medline: 8 5 2023
pubmed: 2 3 2023
entrez: 1 3 2023
Statut: ppublish

Résumé

Elevated plasma concentrations of neural cell adhesion molecule 1 (NCAM1) and p75 neurotrophin receptor (p75) in patients with peripheral neuropathy have been reported. This study aimed to determine the specificity of plasma concentration elevation of either NCAM1 or p75 in a subtype of Charcot-Marie-Tooth disease (CMT) and its correlation with pathologic nerve status and disease severity. Blood samples were collected from 138 patients with inherited peripheral neuropathy and 51 healthy controls. Disease severity was measured using Charcot-Marie-Tooth Neuropathy Score version 2 (CMTNSv2), and plasma concentrations of NCAM1 and p75 were analyzed by enzyme-linked immunosorbent assay. Eight sural nerves from CMT patients were examined to determine the relation of histopathology and plasma NCAM1 levels. Plasma concentration of NCAM1, but not p75, was specifically increased in demyelinating subtypes of CMT (median = 7100 pg/mL, p < 0.001), including CMT1A, but not in axonal subtype (5964 pg/mL, p > 0.05), compared to the control (3859 pg/mL). CMT1A patients with mild or moderate severity (CMTNSv2 < 20) showed higher levels of plasma NCAM1 than healthy controls. Immunofluorescent NCAM1 staining for the sural nerves of CMT patients showed that NCAM1-positive onion bulb cells and possible demyelinating Schwann cells might be associated with the specific increase of plasma NCAM1 in demyelinating CMT. The plasma NCAM1 levels in demyelinating CMT might be a surrogate biomarker reflecting pathological Schwann cell status and disease progression.

Sections du résumé

BACKGROUND AND PURPOSE
Elevated plasma concentrations of neural cell adhesion molecule 1 (NCAM1) and p75 neurotrophin receptor (p75) in patients with peripheral neuropathy have been reported. This study aimed to determine the specificity of plasma concentration elevation of either NCAM1 or p75 in a subtype of Charcot-Marie-Tooth disease (CMT) and its correlation with pathologic nerve status and disease severity.
METHODS
Blood samples were collected from 138 patients with inherited peripheral neuropathy and 51 healthy controls. Disease severity was measured using Charcot-Marie-Tooth Neuropathy Score version 2 (CMTNSv2), and plasma concentrations of NCAM1 and p75 were analyzed by enzyme-linked immunosorbent assay. Eight sural nerves from CMT patients were examined to determine the relation of histopathology and plasma NCAM1 levels.
RESULTS
Plasma concentration of NCAM1, but not p75, was specifically increased in demyelinating subtypes of CMT (median = 7100 pg/mL, p < 0.001), including CMT1A, but not in axonal subtype (5964 pg/mL, p > 0.05), compared to the control (3859 pg/mL). CMT1A patients with mild or moderate severity (CMTNSv2 < 20) showed higher levels of plasma NCAM1 than healthy controls. Immunofluorescent NCAM1 staining for the sural nerves of CMT patients showed that NCAM1-positive onion bulb cells and possible demyelinating Schwann cells might be associated with the specific increase of plasma NCAM1 in demyelinating CMT.
CONCLUSIONS
The plasma NCAM1 levels in demyelinating CMT might be a surrogate biomarker reflecting pathological Schwann cell status and disease progression.

Identifiants

pubmed: 36856547
doi: 10.1111/ene.15763
doi:

Substances chimiques

Biomarkers 0
Neural Cell Adhesion Molecules 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1745-1754

Informations de copyright

© 2023 European Academy of Neurology.

Références

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Auteurs

Young Hee Kim (YH)

Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.

Byeol-A Yoon (BA)

Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.
Department of Neurology, Dong-A University College of Medicine, Busan, Republic of Korea.

Young Rae Jo (YR)

Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.

Soo Hyun Nam (SH)

Stem Cell and Regenerative Medicine Institute, Samsung Medical Center, Seoul, Republic of Korea.

Nam Hee Kim (NH)

Department of Laboratory Medicine, Dong-A University College of Medicine, Busan, Republic of Korea.

Kyoung Hee Kim (KH)

Department of Laboratory Medicine, Dong-A University College of Medicine, Busan, Republic of Korea.

Jong Kuk Kim (JK)

Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.
Department of Neurology, Dong-A University College of Medicine, Busan, Republic of Korea.

Byung-Ok Choi (BO)

Stem Cell and Regenerative Medicine Institute, Samsung Medical Center, Seoul, Republic of Korea.
Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Department of Health Sciences and Technology, The Samsung Advanced Institute for Health Sciences & Technology, Sungkyunkwan University, Seoul, Republic of Korea.

Hwan Tae Park (HT)

Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.
Department of Molecular Neuroscience, Dong-A University College of Medicine, Busan, Republic of Korea.

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