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Updated: Aug 23, 2025

Developing a Rat Model for Bipolar Disorder
Published on: May 2, 2025
Body weight changes and bipolar disorder: a molecular pathway analysis.
Marco Calabró1, Silvana Briuglia1, Concetta Crisafulli1
1Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.
Weight changes in bipolar disorder (BD) are linked to specific molecular pathways involved in energy homeostasis. Identifying these pathways can improve treatment strategies and patient outcomes for individuals with BD.
Area of Science:
- Genetics
- Psychiatry
- Metabolic Disorders
Background:
- Bipolar disorder (BD) is associated with weight-related disorders, influenced by psychological, social, and treatment factors.
- Weight changes in BD impact treatment adherence, quality of life, prognosis, and mortality risk from comorbidities like diabetes and cardiovascular disease.
Purpose of the Study:
- To identify molecular pathways distinguishing individuals with BD who experience weight changes during treatment from those who do not.
- To explore potential biomarkers for predicting and managing weight fluctuations in bipolar disorder.
Main Methods:
- A hypothesis-free molecular pathway analysis was conducted on the STEP-BD sample (n=618).
- Genetic data underwent cluster analysis to control for stratification.
- Clinical covariates including socioeconomic and treatment variables were incorporated.
Main Results:
- No Genome-Wide Association Study significant findings were identified.
- Six molecular pathways were significantly associated with weight change within the first three months of BD treatment.
- Key pathways identified include CDC42 and Rac Family Small GTPase 1, implicated in insulin regulation and diabetes pathophysiology.
Conclusions:
- Molecular pathways central to energy homeostasis may differentiate individuals with BD who experience weight changes during treatment.
- Findings could guide the development of targeted preventive strategies and personalized treatments to enhance BD management and efficacy.
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