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Association of Occupational Dysfunction and Hospital Admissions With Different Polygenic Profiles in Bipolar Disorder
Lina Jonsson1, Elin Hörbeck1, Amedeo Primerano1
1Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden (Jonsson, Hörbeck, Smedler, Pålsson, Sparding, Landén); National Centre for Mental Health, Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, U.K. (Primerano, Craddock, I. Jones, Di Florio); Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm (Song, Karlsson, Sullivan, Landén); Mental Health Center and West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China (Song); Department of Psychological Medicine, University of Worcester, Worcester, U.K. (Gordon-Smith, L. Jones); Departments of Genetics and Psychiatry, University of North Carolina at Chapel Hill (Sullivan).
Polygenic profiles differ for bipolar disorder hospitalizations versus occupational dysfunction. Genetic risk for other psychiatric disorders and education influence work impairment, not bipolar disorder itself.
Area of Science:
- Psychiatry
- Genetics
- Public Health
Background:
- Bipolar disorder (BD) presents with varied severity, including severe mood episodes necessitating hospitalization and long-term occupational dysfunction.
- The genetic underpinnings of these distinct BD outcomes remain unclear.
- Investigating polygenic profiles may elucidate differing etiological pathways.
Purpose of the Study:
- To examine associations between polygenic scores (PGSs) for psychiatric disorders and educational attainment with occupational functioning and psychiatric hospital admissions in individuals with bipolar disorder.
- To determine if distinct polygenic profiles underlie severe mood episodes versus chronic occupational impairment in BD.
Main Methods:
- Utilized Swedish national registers for 4,782 BD patients and 2,963 controls, analyzing over 10 years of longitudinal data.
- Derived measures of unemployment, long-term sick leave, and psychiatric hospital admissions.
- Assessed associations using ordinal regression with PGSs for BD, schizophrenia, major depressive disorder, ADHD, and educational attainment, with replication for hospital admissions.
Main Results:
- Long-term occupational dysfunction (sick leave, unemployment) in BD was linked to PGSs for schizophrenia, ADHD, major depressive disorder, and educational attainment, but not the BD PGS.
- Psychiatric hospital admissions in BD were associated with higher PGSs for bipolar disorder and schizophrenia.
- These findings indicate divergent genetic influences on different BD outcomes.
Conclusions:
- Bipolar disorder severity, measured by hospital admissions, is associated with a distinct polygenic profile compared to long-term occupational dysfunction.
- These results suggest that interventions targeting occupational dysfunction in BD may need to differ from those aimed at preventing mood episodes.
- Understanding these genetic differences could lead to more personalized treatment strategies for bipolar disorder.
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