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Association of Polygenic Risk Score for Suicidal Behavior With Ventral Prefrontal Morphology in Bipolar Disorder
Journal article   Open access   Peer reviewed

Association of Polygenic Risk Score for Suicidal Behavior With Ventral Prefrontal Morphology in Bipolar Disorder

Noa Katz Shroitman, Daniel F Levey, Brian Pittman, Suchen Zheng, Susan Quatrano, Anjali Sankar, Lejla Colic, Joel Gelernter, Virginia L Willour and Hilary P Blumberg
Bipolar disorders, Vol.28(7), e70172
09/09/2026
DOI: 10.1111/bdi.70172
PMCID: PMC13555509
PMID: 42713711
url
https://doi.org/10.1111/bdi.70172View
Published (Version of record) Open Access

Abstract

Bipolar disorder (BD) studies consistently implicate the ventral prefrontal cortex (VPFC) in association with suicidal behaviors. A suicidal behavior polygenic risk score (PRS) can now be computed to test whether elevated genetic risk for suicidal behavior is associated with variation in VPFC gray matter and/or suicidal behavior history. We explored relationships among a PRS previously associated with suicidal behavior, VPFC morphology, and suicidal behavior in 376 individuals of European ancestry (mean age 30y; 57% female): 225 with BD (76 suicide attempters (SAs), 149 non-suicide attempters (NSAs)) and 151 healthy control individuals (HCs). We calculated PRS and performed magnetic resonance imaging to assess VPFC (inferior frontal gyrus (IFG) and orbitofrontal cortex) cortical thickness and surface area. Associations were examined among PRS, diagnosis, suicide attempt history, and brain measures. Among individuals with BD, those with higher PRS showed decreased right VPFC surface area, primarily due to IFG reductions (p < 0.01). A significant group (SA, NSA, HC)-by-PRS interaction was observed for right IFG cortical surface area (p < 0.05); NSAs with high vs. low PRS had significantly smaller right IFG surface area. The mean PRS was highest for SAs, then NSAs, and lowest for HCs; however, differences did not reach significance. These findings suggest this suicide PRS may reflect genetic mechanisms influencing IFG differences in BD. Given the modest sample size, replication of these preliminary findings in large-scale diverse cohorts is required to determine whether including this PRS and/or the corresponding IFG values could improve multimodal BD suicidal behavior prediction algorithms.
Magnetic Resonance Imaging Adult Bipolar Disorder - diagnostic imaging Bipolar Disorder - genetics Bipolar Disorder - pathology Bipolar Disorder - psychology Female Genetic Predisposition to Disease Genetic Risk Score Humans Male Multifactorial Inheritance - genetics Prefrontal Cortex - diagnostic imaging Prefrontal Cortex - pathology Suicide, Attempted - psychology Young Adult

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