Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder

• Published in: PloS one Vol. 10; no. 7; p. e0134202
• Main Authors: Tesli, Martin, Kauppi, Karolina, Bettella, Francesco, Brandt, Christine Lycke, Kaufmann, Tobias, Espeseth, Thomas, Mattingsdal, Morten, Agartz, Ingrid, Melle, Ingrid, Djurovic, Srdjan, Westlye, Lars T, Andreassen, Ole A
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 29.07.2015; Public Library of Science (PLoS)
• Subjects: Abnormalities; Activation; Addictions; Adult; Amygdala; Bipolar disorder; Bipolar Disorder - diagnosis; Bipolar Disorder - genetics; Bipolar Disorder - physiopathology; Brain; Brain - pathology; Brain - physiopathology; Brain mapping; Brain research; Case-Control Studies; Clinical medicine; Consent; Consortia; Cortex (parietal); Cross-Sectional Studies; Diagnosis; Diagnostic systems; Emotions; Emotions - physiology; Face; Facial Expression; Facial Recognition - physiology; Female; Frontal gyrus; Functional magnetic resonance imaging; Functional Neuroimaging; Genetic aspects; Genetics; Hospitals; Humans; Image processing; Magnetic Resonance Imaging; Male; Medical diagnosis; Medicin och hälsovetenskap; Medicine; Mental health; Middle Aged; Multifactorial Inheritance; Multifactorial traits; Multivariate analysis; Neuroimaging; Pattern recognition; Polygenic inheritance; Polymorphism, Single Nucleotide; Psychiatry; Psychosis; Risk Factors; Risk management; Schizophrenia; Studies; Young Adult
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0134202

Bipolar disorder (BD) is a highly heritable disorder with polygenic inheritance. Among the most consistent findings from functional magnetic imaging (fMRI) studies are limbic hyperactivation and dorsal hypoactivation. However, the relation between reported brain functional abnormalities and underlying genetic risk remains elusive. This is the first cross-sectional study applying a whole-brain explorative approach to investigate potential influence of BD case-control status and polygenic risk on brain activation. A BD polygenic risk score (PGRS) was estimated from the Psychiatric Genomics Consortium BD case-control study, and assigned to each individual in our independent sample (N=85 BD cases and 121 healthy controls (HC)), all of whom participated in an fMRI emotional faces matching paradigm. Potential differences in BOLD response across diagnostic groups were explored at whole-brain level in addition to amygdala as a region of interest. Putative effects of BD PGRS on brain activation were also investigated. At whole-brain level, BD cases presented with significantly lower cuneus/precuneus activation than HC during negative face processing (Z-threshold=2.3 as cluster-level correction). The PGRS was associated positively with increased right inferior frontal gyrus (rIFG) activation during negative face processing. For amygdala activation, there were no correlations with diagnostic status or PGRS. These findings are in line with previous reports of reduced precuneus and altered rIFG activation in BD. While these results demonstrate the ability of PGRS to reveal underlying genetic risk of altered brain activation in BD, the lack of convergence of effects at diagnostic and PGRS level suggests that this relation is a complex one.