Poster No:
591
Submission Type:
Abstract Submission
Authors:
Gloria Roberts1, Alistair Perry2, Kate Ridgway1, Vivian Leung1, Megan Campbell3, Rhoshel Lenroot4, Philip Mitchell1, Michael Breakspear3
Institutions:
1University of New South Wales, Sydney, New South Wales, 2University of Cambridge, Cambridge, UK, 3University of Newcastle, Newcastle, New South Wales, 4University of New Mexico, Albuquerque, NM
First Author:
Co-Author(s):
Kate Ridgway
University of New South Wales
Sydney, New South Wales
Vivian Leung
University of New South Wales
Sydney, New South Wales
Introduction:
Recent studies of patients with bipolar disorder or at high genetic risk reveal structural dysconnections among key brain networks supporting cognitive and affective processes (Perry, Roberts et al. 2019). Understanding the longitudinal trajectories of these networks across the peak age range of bipolar disorder onset could inform mechanisms of illness onset or resilience.
Methods:
Longitudinal diffusion-weighted MRI and phenotypic data were acquired at baseline and after 2 years in 183 individuals ages 12–30 years in two cohorts: 97 unaffected individuals with a first-degree relative with bipolar disorder (the high-risk group) and 86 individuals with no family history of mental illness (the control group). Whole-brain structural networks were derived using tractography, and longitudinal changes in these networks were studied using network-based statistics and mixed linear models.
Results:
Both groups showed widespread longitudinal changes, comprising both increases and decreases in structural connectivity, consistent with a shared neurodevelopmental process. On top of these shared changes, high-risk participants showed weakening of connectivity in a network encompassing the left inferior and middle frontal areas, left striatal and thalamic structures, the left fusiform, and right parietal and occipital regions. Connections among these regions strengthened in the control group, whereas they weakened in the high-risk group, shifting toward a cohort with established bipolar disorder. There was marginal evidence for even greater network weakening in those who had their first manic or hypomanic episode before follow-up.
Conclusions:
Neurodevelopment from adolescence into early adulthood is associated with a substantial reorganization of structural brain networks. Differences in these maturational processes occur in a multisystem network in individuals at high genetic risk of bipolar disorder. This may represent a novel candidate to understand resilience and predict conversion to bipolar disorder.
Disorders of the Nervous System:
Psychiatric (eg. Depression, Anxiety, Schizophrenia) 1
Lifespan Development:
Lifespan Development Other 2
Keywords:
Development
DISORDERS
MRI
Psychiatric Disorders
1|2Indicates the priority used for review
Provide references using author date format
Perry*, Roberts*, et al. Connectomics of bipolar disorder: a critical review, and evidence for dynamic
instabilities within interoceptive networks. Mol Psychiatry. 2019;24(9):1296-1318
DOI:10.1038/s41380-018-0267-2