New genomics discoveries across the bipolar disorder spectrum implicate neurobiological and developmental pathways
Bipolar disorder (BD) is a highly heritable mental disorder that affects millions of people worldwide. Our understanding of the genetic etiology and biological processes that underlie BD have greatly increased in recent years. Extensive progress has been made in identifying common variant signals fo...
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
15 August 2025
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| In: |
Biological psychiatry
Year: 2025, Jahrgang: 98, Heft: 4, Pages: 302-310 |
| ISSN: | 1873-2402 |
| DOI: | 10.1016/j.biopsych.2025.05.020 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: https://doi.org/10.1016/j.biopsych.2025.05.020 Verlag, kostenfrei, Volltext: https://www.sciencedirect.com/science/article/pii/S0006322325012193 
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| Verfasserangaben: | Kevin S. O’Connell, Rolf Adolfsson, Till F.M. Andlauer, Michael Bauer, Bernhaud Baune, Joanna M. Biernacka, Bernardo Carpiniello, Sven Cichon, Nick Craddock, Alfredo B. Cuellar-Barboza, Udo Dannlowski, Franziska Degenhardt, Dimitris Dikeos, Panagiotis Ferentinos, Andreas J. Forstner, Mark A. Frye, Janice M. Fullerton, Maria Grigoroiu-Serbanescu, José Guzman-Parra, Lisa Jones, Lina Jonsson, Tilo Kircher, Manolis Kogevinas, Mikael Landén, Jolanta Lissowska, Christine Lochner, Mirko Manchia, Fermin Mayoral, Susan L. McElroy, Nathaniel W. McGregor, Andreas Meyer-Lindenberg, Philip B. Mitchell, Bertram Müller-Myhsok, Markus M. Nöthen, George P. Patrinos, Joanna M. Pawlak, Andreas Reif, Marcella Rietschel, Peter R. Schofield, Thomas G. Schulze, Alessandro Serretti, Jordan W. Smoller, Alessio Squassina, Dan J. Stein, Fabian Streit, Beata Świątkowska, Leonardo Tondo, Eduard Vieta, Irwin D. Waldman, Anders M. Dale, and Ole A. Andreassen, for the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium |
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| 245 | 1 | 0 | |a New genomics discoveries across the bipolar disorder spectrum implicate neurobiological and developmental pathways |c Kevin S. O’Connell, Rolf Adolfsson, Till F.M. Andlauer, Michael Bauer, Bernhaud Baune, Joanna M. Biernacka, Bernardo Carpiniello, Sven Cichon, Nick Craddock, Alfredo B. Cuellar-Barboza, Udo Dannlowski, Franziska Degenhardt, Dimitris Dikeos, Panagiotis Ferentinos, Andreas J. Forstner, Mark A. Frye, Janice M. Fullerton, Maria Grigoroiu-Serbanescu, José Guzman-Parra, Lisa Jones, Lina Jonsson, Tilo Kircher, Manolis Kogevinas, Mikael Landén, Jolanta Lissowska, Christine Lochner, Mirko Manchia, Fermin Mayoral, Susan L. McElroy, Nathaniel W. McGregor, Andreas Meyer-Lindenberg, Philip B. Mitchell, Bertram Müller-Myhsok, Markus M. Nöthen, George P. Patrinos, Joanna M. Pawlak, Andreas Reif, Marcella Rietschel, Peter R. Schofield, Thomas G. Schulze, Alessandro Serretti, Jordan W. Smoller, Alessio Squassina, Dan J. Stein, Fabian Streit, Beata Świątkowska, Leonardo Tondo, Eduard Vieta, Irwin D. Waldman, Anders M. Dale, and Ole A. Andreassen, for the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium |
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| 520 | |a Bipolar disorder (BD) is a highly heritable mental disorder that affects millions of people worldwide. Our understanding of the genetic etiology and biological processes that underlie BD have greatly increased in recent years. Extensive progress has been made in identifying common variant signals for BD, and the polygenic score from the latest genome-wide association study (GWAS) may provide some clinical utility if combined with other risk factors for BD. The role of rare variation in BD remains to be determined, although genes annotated to common variant loci are shown to be enriched for rare variation. BD subtypes have been shown to differ in their genetic architecture, and as such, genetic studies across the subtypes of the BD spectrum will identify subtype-specific signals and reveal subtype-specific biological mechanisms. Despite this, subtype-specific GWAS sample sizes have not increased at the same rate as BD cases, and more concerted efforts are required to obtain this information for participants included in future BD GWASs. Moreover, assessment of culture, geography, and other systematic differences that may impact patient assessment will be necessary to ensure accurate inclusion of diverse ancestral groups and global representation in genetic studies of BD moving forward. | ||
| 650 | 4 | |a Bipolar disorder | |
| 650 | 4 | |a Genetics | |
| 650 | 4 | |a Neurobiology | |
| 650 | 4 | |a Prediction | |
| 650 | 4 | |a Psychiatric genetics | |
| 650 | 4 | |a Variation | |
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