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Corpus callosal morphology in youth with bipolar depression
Author(s) -
MacMaster Frank P,
Langevin Lisa Marie,
Jaworska Natalia,
Kemp Anne,
Sembo Mariko
Publication year - 2014
Publication title -
bipolar disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.285
H-Index - 129
eISSN - 1399-5618
pISSN - 1398-5647
DOI - 10.1111/bdi.12247
Subject(s) - corpus callosum , splenium , white matter , psychology , neuroscience , bipolar disorder , cognition , audiology , magnetic resonance imaging , medicine , radiology
Objectives Recent evidence has demonstrated that corpus callosum maturation follows a similar developmental timeline to cognitive processes. Bipolar disorder ( BD ) has been associated with disruptions in error processing, response inhibition, and motor functioning, which are mediated by underlying white matter structures, including the corpus callosum. Disruptions in white matter integrity have been demonstrated in BD . However, it is unknown whether alterations in the developmental trajectory of the corpus callosum may contribute to cognitive impairments in the disorder. Methods We assessed the area of the corpus callosum and its subregions (the genu, rostral body, anterior and posterior bodies, isthmus, and splenium) in 14 treatment‐naïve adolescents with BD (<21 years of age and in the depressed phase) and 18 healthy adolescent controls. Results In comparison with healthy controls, participants with BD demonstrated a significantly reduced overall corpus callosum area. We also noted smaller areas in the anterior and posterior mid‐body of the corpus callosum in adolescents with BD . Conclusions Our results suggest that commissural fibers of the corpus callosum are disrupted in early‐onset BD . Specific decreases in the anterior and posterior mid‐body callosal aspects may contribute to motor organization and inhibition deficits seen in BD . These findings are consistent with the involvement of inter‐hemispheric tracts in early‐onset BD , which may reflect an early deviation in white matter development.