Clinical and neurostructural characteristics among youth with familial and non-familial bipolar disorder
Autor: | Simina Toma, Lisa Fiksenbaum, Mikaela Dimick, Kody G. Kennedy, Weicong Lu, Alysha Sultan, Benjamin I. Goldstein |
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Rok vydání: | 2021 |
Předmět: |
medicine.medical_specialty
Lithium (medication) business.industry Serotonin reuptake inhibitor Inferior frontal gyrus medicine.disease Amygdala 030227 psychiatry 03 medical and health sciences Psychiatry and Mental health Clinical Psychology 0302 clinical medicine medicine.anatomical_structure Neuroimaging medicine Bipolar disorder Family history business Psychiatry 030217 neurology & neurosurgery Anterior cingulate cortex medicine.drug |
Zdroj: | Journal of Affective Disorders. 282:1315-1322 |
ISSN: | 0165-0327 |
DOI: | 10.1016/j.jad.2020.12.146 |
Popis: | Background Bipolar disorder (BD) is highly heritable and often severe, particularly when illness onset occurs early in life. There is limited knowledge regarding the clinical and neurostructural correlates of family history of BD among youth with BD. Methods Clinical characteristics were evaluated in 197 youth with BD, ages 13-20 years, including 87 with familial BD and 110 with non-familial BD. Structural neuroimaging was examined in a subsample of familial BD (n=39), non-familial BD (n=42), and healthy control (HC, n=58) youth. Region of interest (ROI) analyses of anterior cingulate cortex (ACC), inferior frontal gyrus (IFG), and amygdala were complemented by whole-brain vertex-wise analyses. Results Youth with familial BD had more family history of other psychiatric disorders, less severe worst manic episode, and less treatment with lithium, selective serotonin reuptake inhibitor (SSRI) antidepressants, and any lifetime psychiatric medications. None of these findings survived after correction for multiple comparisons. There were no significant between-group differences in ROI analyses. In whole-brain analyses, significant differences in cortical thickness were as follows: familial and non-familial BD Limitations Relatives did not complete full diagnostic interviews. Conclusions There were relatively few differences in clinical and neurostructural correlates related to family history of BD in youth with BD. Current findings suggest that family history of BD is not a strong contributor to the clinical or neuroimaging phenotypes in youth with BD. |
Databáze: | OpenAIRE |
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