Usefulness of lysophosphatidylcholine measurement in the cerebrospinal fluid for differential diagnosis of neuropathic pain: Possible introduction into clinical laboratory testing.

Cerebrospinal fluid Liquid chromatography-tandem mass spectrometry Lysophosphatidylcholine Neuropathic pain Spinal canal stenosis

Journal

Clinica chimica acta; international journal of clinical chemistry
ISSN: 1873-3492
Titre abrégé: Clin Chim Acta
Pays: Netherlands
ID NLM: 1302422

Informations de publication

Date de publication:
15 Feb 2023
Historique:
received: 05 12 2022
revised: 05 02 2023
accepted: 06 02 2023
pubmed: 11 2 2023
medline: 15 3 2023
entrez: 10 2 2023
Statut: ppublish

Résumé

The differential diagnosis of neuropathic pain, especially discrimination between neuropathic pain caused by spinal canal stenosis (SCS) and neuropathic pain associated with causes other than SCS, is sometimes difficult; however, it is important for surgical application. We established a reliable method for measuring lysophosphatidylcholine (LPC), a precursor of lysophosphatidic acids which are known as being pain initiators, using a liquid chromatography-tandem mass spectrometry method, and measured the LPC concentrations in the cerebrospinal fluid (CSF) in patients with SCS (SCS group; n = 76), patients with neuropathic pain caused by non-SCS diseases (Others group; n = 49), and control subjects without pain (control group; n = 92). Both within-run and between-run CV(%) were almost < 10 %, suggesting an enough performance for clinical introduction. The CSF concentrations of LPC (16:0) and LPC (18:0) were higher in the SCS group than those in the Control or Others group; the concentrations of LPC (18:1), LPC (18:2), LPC (20:4), LPC (22:6) levels were higher in the SCS group than those in the control or others group, but they were also higher in the Others group than those in the control group. The areas under the curve in the ROC curve analyses of LPC (18:1) for discriminating between the SCS and control groups, others and control groups, and SCS and others groups were 0.994, 0.860, and 0.869, respectively. LPC measurement in the CSF is useful for the differential diagnosis of neuropathic pain, especially for surgical decision-making, which is expected for clinical introduction.

Sections du résumé

BACKGROUND BACKGROUND
The differential diagnosis of neuropathic pain, especially discrimination between neuropathic pain caused by spinal canal stenosis (SCS) and neuropathic pain associated with causes other than SCS, is sometimes difficult; however, it is important for surgical application.
METHODS METHODS
We established a reliable method for measuring lysophosphatidylcholine (LPC), a precursor of lysophosphatidic acids which are known as being pain initiators, using a liquid chromatography-tandem mass spectrometry method, and measured the LPC concentrations in the cerebrospinal fluid (CSF) in patients with SCS (SCS group; n = 76), patients with neuropathic pain caused by non-SCS diseases (Others group; n = 49), and control subjects without pain (control group; n = 92).
RESULTS RESULTS
Both within-run and between-run CV(%) were almost < 10 %, suggesting an enough performance for clinical introduction. The CSF concentrations of LPC (16:0) and LPC (18:0) were higher in the SCS group than those in the Control or Others group; the concentrations of LPC (18:1), LPC (18:2), LPC (20:4), LPC (22:6) levels were higher in the SCS group than those in the control or others group, but they were also higher in the Others group than those in the control group. The areas under the curve in the ROC curve analyses of LPC (18:1) for discriminating between the SCS and control groups, others and control groups, and SCS and others groups were 0.994, 0.860, and 0.869, respectively.
CONCLUSIONS CONCLUSIONS
LPC measurement in the CSF is useful for the differential diagnosis of neuropathic pain, especially for surgical decision-making, which is expected for clinical introduction.

Identifiants

pubmed: 36764506
pii: S0009-8981(23)00051-7
doi: 10.1016/j.cca.2023.117249
pii:
doi:

Substances chimiques

Lysophosphatidylcholines 0
Lysophospholipids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117249

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Makoto Kurano (M)

Departments of Clinical Laboratory Medicine, The University of Tokyo, Tokyo, Japan. Electronic address: kurano-tky@umin.ac.jp.

Masahiko Sumitani (M)

Department of Pain and Palliative Medicine, The University of Tokyo Hospital, Tokyo, Japan.

Yoshiyuki Akiyama (Y)

Departments of Urology Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Masaki Yamada (M)

Analytical & Measuring Instruments Division, Shimadzu Corporation, Kyoto, Japan.

Daiki Fujimura (D)

Analytical & Measuring Instruments Division, Shimadzu Corporation, Kyoto, Japan.

Satoshi Yamaki (S)

Analytical & Measuring Instruments Division, Shimadzu Corporation, Kyoto, Japan.

Kuniyuki Kano (K)

Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of.

Junken Aoki (J)

Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of.

Kentaro Hayakawa (K)

Department of Orthopaedic Surgery, Tokyo Metropolitan Geriatric Medical Center, Tokyo, Japan.

Takuya Takahashi (T)

Department of Orthopaedic and Spinal Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Takashi Hirai (T)

Department of Orthopaedic and Spinal Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Atsushi Okawa (A)

Department of Orthopaedic and Spinal Surgery, Tokyo Medical and Dental University, Tokyo, Japan.

Haruki Kume (H)

Departments of Urology Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Toru Ogata (T)

Department of Rehabilitation Medicine, The University of Tokyo, Tokyo, Japan.

Sakae Tanaka (S)

Department of Orthopaedic Surgery, The University of Tokyo Hospital, Japan.

Hirotaka Chikuda (H)

Department of Orthopaedic Surgery, Gunma University, Graduate School of Medicine, Gunma, Japan.

Yutaka Yatomi (Y)

Departments of Clinical Laboratory Medicine, The University of Tokyo, Tokyo, Japan.

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Classifications MeSH