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| Research article summary (published 30 Aug 2009): |
Genetic variation in the G72 (DAOA) gene affects temporal lobe and amygdala structure in subjects affected by bipolar disorder.
Full Abstract
BACKGROUND: Variation in the G72 (DAOA) gene is understood to convey susceptibility for bipolar disorder through an uncertain mechanism. Little is known about the structural brain phenotypes associated with this gene. We hypothesised that reductions in temporal lobe and amygdala gray matter would be associated with variation at two loci in the gene for which evidence of genetic linkage has been repeatedly demonstrated. METHODS: We examined the temporal lobe and amygdala gray matter associations of the risk variants M23 and M24 at the 5' end of the gene encoding G72 in 81 controls and 38 people with bipolar disorder. RESULTS: Genetic variation at both the M23 and M24 loci in G72 were associated with decreased gray matter density within the left temporal pole in people with bipolar disorder. M23 was also associated with reductions in right amygdala gray matter density. The genetic imaging associations were found only in patients with bipolar disorder. CONCLUSIONS: Genetic variation at single nucleotide polymorphisms in the G72 gene previously associated with bipolar disorder is related to reductions in temporal pole and amygdala gray matter structure in people with bipolar disorder.
Author information
Author/s: Zuliani, Riccardo (R); Moorhead, T William J (TW); Job, Dominic (D); McKirdy, James (J); Sussmann, Jessika E D (JE); Johnstone, Eve C (EC); Lawrie, Stephen M (SM); Brambilla, Paolo (P); Hall, Jeremy (J); McIntosh, Andrew M (AM);
Affiliation: Clinica di Psichiatria, Psicologia Medica e Psicosomatica, DPMSC, University of Udine, Udine, Italy.
Journal and publication information
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal: Bipolar disorders (Bipolar Disord), published in Denmark. (Language: eng)
Reference: 2009-Sep; vol 11 (issue 6) : pp 621-7
Dates: Created 2009/08/19; Completed 2009/11/05;
PMID: 19689504, status: MEDLINE (last retrieval date: 11/5/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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