Evidence map›Paper›PMID 42352582›Full record

ArticleBrain sciences2026

Lysophosphatidic Acid 18:0 sn-1 in Cerebrospinal Fluid as a Potential Biomarker of Depressive Symptoms in Patients with Neuropathic Pain.

Reo Inoue, Masahiko Sumitani, Atsushi Kimura, Takao Mochizuki, Toru Akiyama, Yoshifumi Morita, Takuya Takahashi, Takashi Hirai, Kentaro Hayakawa, Hirotaka Chikuda and 1 more

Abstract read
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Article in Brain sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Reo InoueDepartment of Anesthesiology and Pain Relief Center, The University of Tokyo Hospital, Bunkyo 113-0033, Japan.ORCID 0000-0001-5093-4379
Masahiko SumitaniDepartment of Pain and Palliative Medicine, The University of Tokyo Hospital, Bunkyo 113-0033, Japan.ORCID 0000-0002-3662-8217
Atsushi KimuraDepartment of Orthopaedic Surgery, Jichi Medical University, Shimotsuke 329-0498, Japan.ORCID 0000-0003-4948-1792
Takao MochizukiDepartment of Orthopaedic Surgery, Saitama Medical Center, Jichi Medical University, Omiya 330-0834, Japan.
Toru AkiyamaDepartment of Orthopaedic Surgery, Saitama Medical Center, Jichi Medical University, Omiya 330-0834, Japan.
Yoshifumi MoritaDepartment of Clinical Laboratory Medicine, The University of Tokyo Hospital, Bunkyo 113-0033, Japan.ORCID 0000-0001-9129-0223
Takuya TakahashiDepartment of Orthopaedic and Spinal Surgery, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Bunkyo 113-8519, Japan.
Takashi HiraiDepartment of Orthopaedic and Spinal Surgery, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Bunkyo 113-8519, Japan.ORCID 0000-0001-6200-0100
Kentaro HayakawaDepartment of Orthopaedics and Spine Surgery, Tokyo Metropolitan Institute for Geriatrics and Gerontology, Itabashi 173-0015, Japan.ORCID 0000-0001-7450-7339
Hirotaka ChikudaDepartment of Orthopaedic Surgery, Gunma University, Maebashi 371-8511, Japan.ORCID 0000-0002-7913-1542
Makoto KuranoDepartment of Clinical Laboratory Medicine, The University of Tokyo Hospital, Bunkyo 113-0033, Japan.

Funding

Japan Agency for Medical Research and Development 22ek0610028h0001 and 19lm0203084h001
6 · The paper itself

Abstract

BACKGROUND/

objectivesLysophosphatidic acid (LPA) is a bioactive lipid mediator implicated in neuropathic pain (NP). Depressive symptoms frequently accompany NP and adversely affect outcomes, yet objective biomarkers remain limited. This study aimed to identify cerebrospinal fluid (CSF) LPA molecular species associated with depressive symptoms in patients with NP.

methodsCSF samples were obtained from 48 patients, and LPA species, including positional isomers (sn-1 and sn-2), were quantified using liquid chromatography-tandem mass spectrometry. Depressive symptoms were assessed using the depression subscale of the Hospital Anxiety and Depression Scale (HADS-D). Statistical analyses were performed to evaluate associations among depressive symptoms, clinical variables, and LPA species.

resultsCSF LPA18:0 was significantly associated with HADS-D scores (r = 0.380,

conclusionsThese findings suggest that CSF LPA18:0 sn-1 may be associated with a biological dimension of depressive distress and may represent a candidate biomarker of depressive distress in NP. However, these findings should be interpreted cautiously, as the analyses were exploratory, and further validation in independent and longitudinal cohorts is warranted.

Indexed as

cerebrospinal fluiddepressive symptomsLPAlysophosphatidic acidneuropathic pain

Identifiers

PMID42352582
PMCPMC13296637

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