کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5844776 | 1561053 | 2013 | 6 صفحه PDF | دانلود رایگان |
BackgroundMajor depressive disorder (MDD) is shown to have structural and functional abnormalities in specific brain areas and connections by recent neuroimaging studies. However, little is known about the alterations of the interhemispheric resting-state functional connectivity (FC) in patients with MDD. In the present study, we used a newly developed voxel-mirrored homotopic connectivity (VMHC) method to investigate the interhemispheric FC of the whole brain in patients with MDD at rest.MethodsTwenty-four first-episode, drug-naive patients with MDD and 24 age-, gender-, and education-matched healthy subjects underwent a resting-state functional magnetic resonance imaging (fMRI). An automated VMHC approach was used to analyze the data.ResultsPatients with MDD showed lower VMHC than healthy subjects in the medial prefrontal cortex (MPFC) and the posterior cingulate cortex/precuneus (PCC/PCu), two core regions within default mode network (DMN). Both left and right MPFC showed reduced FC with the other frontal areas and with right anterior cingulate gyrus (ACC), while PCC/PCu exhibited abnormal FC with the frontal areas and thalamus in patient group. Significant positive correlation was observed between VMHC in MPFC and persistent error response of Wisconsin Card Sorting Test (WCST-Pre) in patients. Further ROC analysis revealed that VMHC in the MPFC and PCC/PCu could be used to differentiate the patients from healthy subjects with relatively high sensitivity and specificity.ConclusionsOur results suggest that decreased VMHC in brain regions within DMN may underlie the pathogenesis of MDD.
⺠Little is known about the alterations of the interhemispheric resting-state FC in MDD. ⺠Patients with MDD enrolled were first episode, drug-naive patients. ⺠VMHC was used to investigate the interhemispheric FC of the whole brain in MDD. ⺠Decreased VMHC within DMN may underlie the pathogenesis of MDD.
Journal: Progress in Neuro-Psychopharmacology and Biological Psychiatry - Volume 41, 5 March 2013, Pages 24-29