Abnormal resting-state cerebral-limbic functional connectivity in bipolar depression and unipolar depression

• Published in: BMC neuroscience 2019-06, Vol.20 (1), p.30-30, Article 30
• Main Authors: Liu, Chang, Pu, Weidan, Wu, Guowei, Zhao, Jie, Xue, Zhimin
• Format: Article
• Language: English
• Subjects: Adult; Amygdala; Analysis; Biological markers; Bipolar disorder; Bipolar Disorder - physiopathology; Brain; Brain mapping; Care and treatment; Case-Control Studies; Cerebral cortex; Cerebral Cortex - physiopathology; Cerebral-limbic; Cortex (parietal); Depression; Depressive Disorder - physiopathology; Education; Emotional disorders; Emotions; Female; Frontal gyrus; Functional activity; Functional magnetic resonance imaging; Functional Neuroimaging; Humans; Limbic System - physiopathology; Magnetic Resonance Imaging; Male; Mental depression; Neural circuitry; Neural networks; Neural Pathways - physiopathology; Neurobiology; Neurophysiology; NMR; Nuclear magnetic resonance; Patients; Psychiatry; Resting-state; Risk factors; Severity of Illness Index; Superior temporal gyrus; Temporal cortex; Temporal gyrus; Thalamus; Young Adult
• ISSN: 1471-2202; 1471-2202
• DOI: 10.1186/s12868-019-0508-6

Distinctive patterns of functional connectivity (FC) abnormalities in neural circuitry has been reported in patients with bipolar depression (BD) and unipolar depression (UD). However, it is unclear that whether this distinct functional connectivity patterns are diagnosis specific between BD and UD. This study aimed to compare patterns of functional connectivity among BD, UD and healthy controls (HC) and determine the distinct functional connectivity patterns which can differentiate BD from UD. Totally 23 BD, 22 UD, and 24 HC were recruited to undergo resting-state fMRI scanning. FC between each pair of brain regions was calculated and compared among the three groups, the associations of FC with depressive symptom were also analyzed. Both patient groups showed significantly decreased cerebral-limbic FC located between the default mode network [posterior cingulated gyrus (PCG) and precuneus] and limbic regions (hippocampus, amygdala and thalamus) than HC. Moreover, the BD group exhibited more decreased FC mainly in the cortical regions (middle temporal gyrus, PCG, medial superior frontal gyrus, inferior occipital gyrus and superior temporal gyrus), but the UD group is more associated with limbic alterations. These decreased FCs were negatively correlated with HAMD scores in both BD and UD patients. BD and UD patients demonstrate different patterns of abnormal cerebral-limbic FC, reflected by decreased FC within cerebral cortex and limbic regions in BD and UD, respectively. The distinct FC abnormal pattern of the cerebral-limbic circuit might be applied as biomarkers to differentiate these two depressive patient groups.