Moving toward precision and personalized treatment strategies in psychiatry
- PMID: 40255203
- PMCID: PMC12084835
- DOI: 10.1093/ijnp/pyaf025
Moving toward precision and personalized treatment strategies in psychiatry
Abstract
Precision psychiatry aims to improve routine clinical practice by integrating biological, clinical, and environmental data. Many studies have been performed in different areas of research on major depressive disorder, bipolar disorder, and schizophrenia. Neuroimaging and electroencephalography findings have identified potential circuit-level abnormalities predictive of treatment response. Protein biomarkers, including IL-2, S100B, and NfL, and the kynurenine pathway illustrate the role of immune and metabolic dysregulation. Circadian rhythm disturbances and the gut microbiome have also emerged as critical transdiagnostic contributors to psychiatric symptomatology and outcomes. Moreover, advances in genomic research and polygenic scores support the perspective of personalized risk stratification and medication selection. While challenges remain, such as data replication issues, prediction model accuracy, and scalability, the progress so far achieved underscores the potential of precision psychiatry in improving diagnostic accuracy and treatment effectiveness.
Keywords: biomarkers; bipolar disorder; major depression; personalized medicine; schizophrenia.
© The Author(s) 2025. Published by Oxford University Press on behalf of CINP.
Conflict of interest statement
A.S. is or has been a consultant to or has received honoraria or grants unrelated to the present work from: Abbott, AbbVie, Angelini, Astra Zeneca, Clinical Data, Boheringer, Bristol Myers Squibb, Eli Lilly, GlaxoSmithKline, Innova Pharma, Italfarmaco, Janssen, Lundbeck, Naurex, Pfizer, Polifarma, Sanofi, Servier, Taliaz. B.B. received honoraria for serving as a consultant or on advisory boards unrelated to the present work for Angelini, AstraZeneca, Biogen, Boehringer Ingelheim, Bristol-Meyers Squibb, Janssen, LivaNova, Lundbeck, Medscape, Neurotorium, Novartis, Otsuka, Pfizer, Recordati, Roche, Rovi, Sanofi, Servier, Teva. D.R. served as a consultant for Janssen, received honoraria from Gerot-Lannacher, Janssen, and Pharmagenetix, received travel support from Angelini and Janssen, and served on advisory boards of AC Immune, Roche, and Rovi. S.C. has received grant support from MGGM LLC, and consultant fees from Neuroarbor LLC and MGGM LLC, companies affiliated with Relmada Therapeutics, and from Dompè farmaceutici S.p.A. M.M. has received honoraria unrelated to the present work from Angelini, Lundbeck, Fidia, Rovi, Viatris, Johnson and Johnson.
The remaining authors have no conflict of interest to declare.
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