Publication: Mechanisms of weight gain associated with valproic acid: a scoping review
Program
KU-Authors
KU Authors
Co-Authors
Popkova, D.
Fellendorf, F.
Vinberg, M.
Bukova-Zideluna, A.
Fleischmann, E.
Dalkner, N.
Tmava-Berisha, A.
Lenger, M.
Manchia, M.
Reininghaus, E.
Editor & Affiliation
Compiler & Affiliation
Translator
Other Contributor
Date
Language
eng
Type
Embargo Status
N/A
Journal Title
Journal ISSN
Volume Title
Alternative Title
Abstract
Valproic acid (VPA), a widely prescribed mood stabilizer and antiepileptic drug, is frequently associated with metabolic side effects, particularly weight gain. Despite its clinical relevance, the range and diversity of mechanisms underlying VPA-associated weight gain remain incompletely mapped. Objectives To map the breadth of evidence on mechanisms of VPA-associated weight gain, characterize the types of studies and populations investigated, and identify knowledge gaps to inform future research. Methods This PRISMA-ScR-guided scoping review searched PubMed, Cochrane Library, Scopus, and Google Scholar for studies on VPA-weight gain mechanisms in adults. One reviewer charted data using a piloted form; two independently assessed quality (Newcastle-Ottawa Scale). Sources were grouped by mechanistic pathway with descriptive summaries and vote-counting. Results Fifteen studies ( n = 1,339 participants) were included, representing diverse designs: cross-sectional ( n = 4), prospective observational ( n = 3), genetic association ( n = 2), and others. Evidence mapped to three primary mechanistic domains: hormonal dysregulation (like elevated insulin, leptin, insulin resistance, and other findings); genetic predispositions, including CYP2C19 polymorphisms, CRTC1 methylation, and other genetic variants; and lipid metabolism alterations (increased TC, LDL-C, TG, FFAs; decreased Apo A1; mixed HDL-C findings). Hormonal and lipid pathways are well-documented, while genetic mechanisms require validation in larger, standardized cohorts. Conclusions This scoping review identifies a heterogeneous evidence base with well-established hormonal and lipid mechanisms and emerging genetic pathways. Key gaps include underrepresentation of bipolar disorder populations, limited longitudinal genetic studies, and lack of integrated frameworks combining hormonal, genetic, and metabolic data. Findings inform future research priorities and highlight the need for personalized monitoring strategies.
Source
Publisher
Springer
Subject
Health sciences, Medicine, Neurosciences, Neurology, Psychiatry
Citation
Has Part
Source
European Archives of Psychiatry and Clinical Neuroscience
Book Series Title
Edition
DOI
10.1007/s00406-026-02295-x
item.page.datauri
Link
Rights
N/A
Copyrights Note
Creative Commons license
Except where otherwised noted, this item's license is described as N/A
