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| Research article summary (published 30 Aug 2009): |
Corpus callosum size and shape in established bipolar affective disorder.
Full Abstract
OBJECTIVE: Callosal structural and functional alterations have been demonstrated in a range of neuropsychiatric illnesses, including bipolar disorder, but no study has examined regional callosal thickness in this phenotype. The aim of the present study was therefore to examine callosal size and shape in a well-defined group of bipolar affective disorder patients and controls. METHODS: The participants included 24 patients with DSM-IV bipolar I disorder and 24 matched healthy controls. The corpus callosum was extracted from mid-callosal images from T1-weighted magnetic resonance imaging scans on all participants, and callosal area, length, bending angle and regional callosal thickness measures were computed from these images. RESULTS: The callosum was thinner in the bipolar group overall, with a disproportionately reduced thickness in the splenium. Psychotic and non-psychotic patients did not differ, although patients without a family history of mood disorders had a thinner callosum. CONCLUSION: Callosal reductions are present in established bipolar disorder, and affect posterior regions more than anterior regions. This may reflect a primary disturbance to myelination, or a secondary effect of grey matter changes.
Author information
Author/s: Walterfang, Mark (M); Malhi, Gin S (GS); Wood, Amanda G (AG); Reutens, David C (DC); Chen, Jian (J); Barton, Sarah (S); Yücel, Murat (M); Velakoulis, Dennis (D); Pantelis, Christos (C);
Affiliation: Melbourne Neuropsychiatry Centre, University of Melbourne, Melbourne, Victoria 3050, Australia. mark.walterfang(-atsign-)mh.org.au
Journal and publication information
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
Journal: The Australian and New Zealand journal of psychiatry (Aust N Z J Psychiatry), published in England. (Language: eng)
Reference: 2009-Sep; vol 43 (issue 9) : pp 838-45
Dates: Created 2009/08/11; Completed 2009/10/21;
PMID: 19670057, status: MEDLINE (last retrieval date: 10/21/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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