Evidence map›Paper›PMID 40278404›Full record

ArticleMetabolites2025

Targeted and Non-Targeted Metabolomic Evaluation of Cerebrospinal Fluid in Early Phase Schizophrenia: A Pilot Study from the Hopkins First Episode Psychosis Project.

George E Jaskiw, Mark E Obrenovich, Curtis J Donskey, Farren B S Briggs, Sun Sunnie Chung, Anastasiya I Kalinina, Austin Bolomey, Lindsay N Hayes, Kun Yang, Robert H Yolken and 1 more

Abstract read
In one paragraph

Article in Metabolites, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

George E JaskiwVeterans Affairs Northeast Ohio Healthcare System, Cleveland, OH 44106, USA.ORCID 0000-0001-7168-0822
Mark E ObrenovichVeterans Affairs Northeast Ohio Healthcare System, Cleveland, OH 44106, USA.
Curtis J DonskeyVeterans Affairs Northeast Ohio Healthcare System, Cleveland, OH 44106, USA.
Farren B S BriggsDepartment Public Health Sciences, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.ORCID 0000-0003-0903-1359
Sun Sunnie ChungDepartment of Computer Science, Cleveland State University, Cleveland, OH 44115, USA.ORCID 0000-0002-6295-4593
Anastasiya I KalininaDepartment of Computer Science, Cleveland State University, Cleveland, OH 44115, USA.
Austin BolomeyVeterans Affairs Northeast Ohio Healthcare System, Cleveland, OH 44106, USA.
Lindsay N HayesDepartment of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.ORCID 0000-0001-6314-6451
Kun YangDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Robert H YolkenStanley Division of Developmental Neurovirology, Johns Hopkins School of Medicine, The Johns Hopkins Hospital, Baltimore, MD 21287, USA.
Akira SawaDepartments of Psychiatry, Neuroscience, Biomedical Engineering, Pharmacology, Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

Funding

Project 3P50MH094268 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SAWA, AKIRA · 2011 to 2020
$19.9M
Project 3P50MH136297 · NIMH · JOHNS HOPKINS UNIVERSITY · PI Akira Sawa · 2024 to 2026
$12.8M
High throughput marker for cognitive deficit: cellular autofluorescenceR01MH107730 · NIMH · JOHNS HOPKINS UNIVERSITY · PI SAWA, AKIRA · 2018 to 2022
$3.0M
NIMH NIH HHS P50 MH094268NIMH NIH HHS P50 MH136297NIMH NIH HHS R01 MH107730
6 · The paper itself

Abstract

(1) Background: The lack of reliable biomarkers remains a significant barrier to improving outcomes for patients with schizophrenia. While metabolomic analyses of blood, urine, and feces have been explored, results have been inconsistent. Compared to peripheral compartments, cerebrospinal fluid (CSF) more closely reflects the chemical composition of brain extracellular fluid. Given that brain dysregulation may be more pronounced during the first episode of psychosis (FEP), we hypothesized that metabolomic analysis of CSF from FEP patients could reveal disease-associated biomarkers. (2) Methods: We recruited 15 patients within 24 months of psychosis onset (DSM-4 criteria) and 14 control participants through the Johns Hopkins Schizophrenia Center. CSF samples were analyzed using both non-targeted and targeted liquid chromatography-mass spectrometry. (3) Results: The non-targeted analysis identified lower levels of N-acetylneuraminic acid and N-acetyl-L-aspartic acid in the FEP group, while levels of uric acid were elevated. The targeted analysis focused on indolic and phenolic molecules previously linked to neuropsychiatric disorders. Notably, L-phenylalanine and 4-hydroxycinnamic acid levels were lower in the FEP group, and this difference remained significant after adjusting for age and sex. However, none of the significant differences in analyte levels between the groups survived an adjustment for multiple comparisons. (4) Conclusions: Our intriguing but preliminary associations align with results from other investigational approaches and highlight potential CSF analytes that warrant further study in larger samples.

Indexed as

biomarkercerebrospinal fluidfirst-episode psychosisgut microbiomemetabolomenon-targetedschizophreniatargeted

Identifiers

PMID40278404
PMCPMC12029220

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.