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. 2009 Sep 1;66(5):451-9.
doi: 10.1016/j.biopsych.2009.03.024. Epub 2009 May 17.

Abnormal amygdala-prefrontal effective connectivity to happy faces differentiates bipolar from major depression

Affiliations

Abnormal amygdala-prefrontal effective connectivity to happy faces differentiates bipolar from major depression

Jorge Renner Cardoso de Almeida et al. Biol Psychiatry. .

Abstract

Background: Bipolar disorder is frequently misdiagnosed as major depressive disorder, delaying appropriate treatment and worsening outcome for many bipolar individuals. Emotion dysregulation is a core feature of bipolar disorder. Measures of dysfunction in neural systems supporting emotion regulation might therefore help discriminate bipolar from major depressive disorder.

Methods: Thirty-one depressed individuals-15 bipolar depressed (BD) and 16 major depressed (MDD), DSM-IV diagnostic criteria, ages 18-55 years, matched for age, age of illness onset, illness duration, and depression severity-and 16 age- and gender-matched healthy control subjects performed two event-related paradigms: labeling the emotional intensity of happy and sad faces, respectively. We employed dynamic causal modeling to examine significant among-group alterations in effective connectivity (EC) between right- and left-sided neural regions supporting emotion regulation: amygdala and orbitomedial prefrontal cortex (OMPFC).

Results: During classification of happy faces, we found profound and asymmetrical differences in EC between the OMPFC and amygdala. Left-sided differences involved top-down connections and discriminated between depressed and control subjects. Furthermore, greater medication load was associated with an amelioration of this abnormal top-down EC. Conversely, on the right side the abnormality was in bottom-up EC that was specific to bipolar disorder. These effects replicated when we considered only female subjects.

Conclusions: Abnormal, left-sided, top-down OMPFC-amygdala and right-sided, bottom-up, amygdala-OMPFC EC during happy labeling distinguish BD and MDD, suggesting different pathophysiological mechanisms associated with the two types of depression.

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Conflict of interest statement

Financial Disclosures

DrPhillips reports having support from NARSAD Independent Investigator Award and 5R01 MH076971-01. DrAlmeida reports having support from CAPES foundation (#190105-2). DrHassel reports having support from NARSAD. DrMechelli, DrVersace, DrQuevedo and DrKupfer reported no biomedical financial interests or potential conflicts of interest.

Figures

Figure 1
Figure 1. Schematic representation of the dynamic causal modeling
The face presentation entered (yellow arrow) the dynamic causal model through the amygdala and propagated to OMPFC via bottom-up (red arrow), and back to the amygdala via top-down (blue arrow) interconnections between the two regions through the unicinate fasciculus. AMY: amygdala; OMPFC: orbitomedial pre-frontal cortex; A: anterior; P: posterior; L: left and R: right side of the brain
Figure 2
Figure 2. Effective Connectivity (EC) between OMPFC and amygdala
A. Representation of the bottom-up (red arrow) and top-down (blue arrow) endogenous connection between left amygdala and left OMPFC B. Left-sided top-down OMPFC-amygdala EC in the happy experiment Happy experiment: negative EC in MDD relative to HC (**U=52, p=0.004; d=0.95) A close to zero effective connectivity in BD when relative to HC (**U=52, p=0.007; d=0.65). There were no difference between the two depressed groups on this EC measure (*U=83; p=0.14; d=0.67). C. Right-sided bottom-up amygdala-OMPFC EC in the happy experiment Happy experiment: reduced EC in MDD relative to HC (**U=110, p=0.5; d=0.37). A close to zero effective connectivity in BD relative to HC (**U=42, p=0.002; d=1.2). There was a trend difference between the two depressed groups on this EC measure (*U=64; p=0.027; d=0.42).

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