期刊
BIOLOGICAL PSYCHIATRY
卷 70, 期 4, 页码 343-349出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2011.04.007
关键词
Amygdala; bipolar disorder; fMRI; prefrontal; striatum
资金
- Royal Society [DH080018]
- Health Foundation [2268/4295]
- National Alliance for Research on Schizophrenia and Depression Independent Investigator Award
- Wellcome Trust [087727/Z/08/Z]
- Chief Scientists Office in Scotland
- SINAPSE (Scottish Imaging Network, a Platform for Scientific Excellence)
- National Health Service (NHS) Research Scotland, through the Scottish Mental Health Research Network
- Pfizer
- Royal Society [DH080018] Funding Source: Royal Society
- MRC [G0600429] Funding Source: UKRI
- Medical Research Council [G0600429] Funding Source: researchfish
- Wellcome Trust [087727/Z/08/Z] Funding Source: Wellcome Trust
Background: Bipolar disorder is a highly heritable psychiatric disorder characterized by episodic elevation or depression of mood. Bipolar disorder is associated with structural and functional brain abnormalities but it is unclear whether these are present in relatives of affected individuals and if they are associated with subclinical symptoms or traits associated with the disorder. Methods: Functional magnetic resonance imaging scans were conducted on 93 unrelated relatives of bipolar disorder patients and 70 healthy comparison subjects performing the Hayling sentence completion paradigm. Examination of comparison subjects versus high-risk individuals was followed by assessments of associations with depression scores and measures of cyclothymic temperament. Results: Examination of comparison subjects versus high-risk subjects revealed increased activation in the high-risk group in the left amygdala. No interaction effects were observed between the groups for scores of depression or cyclothymia and activation in any region. Significant associations were found across the groups with depression ratings and activation in the ventral striatum and with cyclothymia and activation in ventral prefrontal regions, however no interaction effects were observed between the groups. Conclusions: Differences in activation in the left amygdala in those at familial risk may represent a heritable endophenotype of bipolar disorder. Activation in striatal and ventral prefrontal regions may, in contrast, represent a distinct biological basis of subclinical features of the illness regardless of the presence of familial risk.
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