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Updated: Mar 24, 2026

Developing a Rat Model for Bipolar Disorder
Published on: May 2, 2025
Melatonin receptor 1B gene associated with hyperglycemia in bipolar disorder
Dzana S Hukic1, Catharina Lavebratt, Louise Frisén
1aNeurogenetics Unit, Department of Molecular Medicine and Surgery bDepartment of Clinical Neuroscience cEndocrine and Diabetes Unit, Department of Molecular Medicine and Surgery dCardiovascular Medicine Unit, Department of Medicine eDepartment of Neurobiology, Care Sciences and Society, Centre for Family Medicine fCentre for Psychiatric Research and Education, Karolinska Institutet gCenter for Molecular Medicine, Karolinska University Hospital Solna hChild and Adolescent Psychiatry Research Center, Stockholm iDepartment of Clinical Sciences, Lund University, Lund, Sweden.
Abstract:
Bipolar patients are at a higher risk of developing metabolic disorders. Cardiovascular morbidity and mortality is twice the rate reported in the population. Antipsychotic medication increases the risk of metabolic abnormalities. However, bipolar disorder and schizophrenia have a similarly increased mortality from cardiovascular causes of death, although bipolar patients medicate with antipsychotic drugs to a much smaller extent than schizophrenic patients. Bipolar disorder and schizophrenia share substantial genetic risk components; thus, increased metabolic abnormalities is hypothesized to be an effect of specific sets of metabolic risk genes, which might overlap with the metabolic risk genes in schizophrenia. This study reports that a functional genetic variant of MTNR1B, previously implicated in the impairment of glucose-stimulated insulin release also in schizophrenia, was associated with elevated fasting glucose levels in bipolar patients and controls. This finding suggests that the MTNR1B-dependent vulnerability for elevated fasting plasma glucose levels is shared between bipolar disorder and schizophrenia.
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