Evidence map›Paper›PMID 41767152›Full record

ReviewFrontiers in psychiatry2026

Metabolomics biomarkers for precision psychiatry.

Daniele Cavaleri, Carlo Bassetti, Giorgio Cucchi, Pasquale De Fazio, Renato de Filippis, Umberto Albert, Luca Pellegrini, Giuseppe Carrà, Francesco Bartoli

Abstract readReview
In one paragraph

Review in Frontiers in psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
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

9 authors.

Daniele CavaleriSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Carlo BassettiSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Giorgio CucchiSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Pasquale De FazioDepartment of Health Sciences, University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Renato de FilippisDepartment of Health Sciences, University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
Umberto AlbertDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
Luca PellegriniDepartment of Medicine, Surgery and Health Sciences, University of Trieste, Trieste, Italy.
Giuseppe CarràSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Francesco BartoliSchool of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mental disorders remain diagnosed primarily through symptom-based classification systems that overlook biological heterogeneity, preventing the identification of mechanistically distinct patient subgroups and precluding pathophysiology-guided treatment selection. Metabolomics offers a promising pathway towards precision psychiatry by capturing dynamic biochemical readouts at the functional endpoint of the omics cascade, integrating genetic, environmental, and pharmacological influences on cellular metabolism. Over the past 15 years, untargeted and targeted metabolomics studies using nuclear magnetic resonance spectroscopy and mass spectrometry have identified consistent patterns of metabolic dysregulation across psychiatric disorders, particularly involving amino acid metabolism, lipid signaling, energy homeostasis, and oxidative stress pathways. Schizophrenia presents disruptions in arginine and proline metabolism, glutathione metabolism, and energy-related processes. Bipolar disorder shows perturbations in branched-chain and aromatic amino acids, kynurenine pathway, and tricarboxylic acid cycle dysfunction with phase-specific metabolic signatures. Major depressive disorder exhibits widespread alterations in amino acid turnover, bioenergetic processes, membrane lipid homeostasis, and glutamate-GABA cycling, with treatment-responsive metabolic changes. Despite these advances, substantial challenges remain: heterogeneous findings with disorder overlap, limited replication cohorts, predominance of cross-sectional designs, confounding by medication and lifestyle factors, pre-analytical variability, and high-dimensional data complexity. Future research requires harmonized multi-site protocols, longitudinal validation studies, multi-platform analytical approaches, integration with genomics, proteomics, and digital phenotyping, and implementation of artificial intelligence frameworks to enhance phenotype discrimination and predictive accuracy. In this mini-review, we provide an overview of current methodologies, major findings, strengths, challenges, and emerging directions in psychiatric metabolomics, with the goal of facilitating the translation of metabolomic insights into clinically applicable, personalized psychiatric treatment.

Indexed as

anxiety disordersbiomarkersbipolar disordermajor depressive disordermetabolomicsobsessive-compulsive disorderpost-traumatic stress disorderschizophrenia

Identifiers

PMID41767152
PMCPMC12946017

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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.