TY - JOUR
T1 - Executive function mediates prefrontal excitation-inhibition balance and emotion recognition in euthymic bipolar disorder
AU - Wu, Cheng Ying
AU - Chang, Chih Yu
AU - Wei, Shyh Yuh
AU - Chang, Hui Hua
AU - Tsai, Ying Tsung
AU - Lu, Tsung-Hua
AU - Lin, Ren Yi
AU - Yang, Yen Kuang
AU - Chen, Po See
AU - Huang, Yu Lien
AU - Tseng, Huai Hsuan
N1 - Publisher Copyright:
© The Author(s), 2025.
PY - 2025/10/10
Y1 - 2025/10/10
N2 - Background Euthymic bipolar disorder (euBD) patients exhibit deficits in neurocognitive and social cognitive functioning compared to healthy controls (HCs). Our prior research has shown that the excitatory/inhibitory (E/I) imbalance in the default mode network (DMN) is linked to executive function in euBD. Neurocognitive impairments are associated with social cognition deficits in individuals with mental disorders. Given this connection, this study posits E/I imbalance within the DMN is associated with social cognition, with executive function as a mediator. Methods Seventy-five HCs and 49 euBD individuals were recruited. Using the emotion recognition task, Diagnostic Analysis of Nonverbal Accuracy 2-Taiwan version (DANVA-2-TW) and cognitive flexibility task, Wisconsin Card Sorting Test (WCST), we assessed emotion recognition and prefrontal function. Proton magnetic resonance spectroscopy (1H-MRS) measured metabolites in the posterior cingulate cortex (PCC) and medial prefrontal cortex/anterior cingulate cortex (mPFC/ACC), quantifying excitatory glutamate+glutamine (Glx) and inhibitory GABA to calculate the E/I ratio. Results euBD patients showed poorer emotion recognition (p = 0.020) and poorer cognitive flexibility (fewer WCST categories completed, p = 0.002). A negative association was found between emotion recognition and the E/I ratio in the mPFC/ACC of the BD patients (r = -0.30, p = 0.034), which was significantly mediated by cognitive flexibility (Z = -2.657, p = 0.007). Conclusion The BD patients demonstrate deficits in emotion recognition, linked to an altered E/I balance in the prefrontal cortex, and the cognitive flexibility, a key aspect of executive function, mediates the impact of the E/I ratio on emotion recognition accuracy in euBD patients.
AB - Background Euthymic bipolar disorder (euBD) patients exhibit deficits in neurocognitive and social cognitive functioning compared to healthy controls (HCs). Our prior research has shown that the excitatory/inhibitory (E/I) imbalance in the default mode network (DMN) is linked to executive function in euBD. Neurocognitive impairments are associated with social cognition deficits in individuals with mental disorders. Given this connection, this study posits E/I imbalance within the DMN is associated with social cognition, with executive function as a mediator. Methods Seventy-five HCs and 49 euBD individuals were recruited. Using the emotion recognition task, Diagnostic Analysis of Nonverbal Accuracy 2-Taiwan version (DANVA-2-TW) and cognitive flexibility task, Wisconsin Card Sorting Test (WCST), we assessed emotion recognition and prefrontal function. Proton magnetic resonance spectroscopy (1H-MRS) measured metabolites in the posterior cingulate cortex (PCC) and medial prefrontal cortex/anterior cingulate cortex (mPFC/ACC), quantifying excitatory glutamate+glutamine (Glx) and inhibitory GABA to calculate the E/I ratio. Results euBD patients showed poorer emotion recognition (p = 0.020) and poorer cognitive flexibility (fewer WCST categories completed, p = 0.002). A negative association was found between emotion recognition and the E/I ratio in the mPFC/ACC of the BD patients (r = -0.30, p = 0.034), which was significantly mediated by cognitive flexibility (Z = -2.657, p = 0.007). Conclusion The BD patients demonstrate deficits in emotion recognition, linked to an altered E/I balance in the prefrontal cortex, and the cognitive flexibility, a key aspect of executive function, mediates the impact of the E/I ratio on emotion recognition accuracy in euBD patients.
UR - https://www.scopus.com/pages/publications/105018398103
UR - https://www.scopus.com/pages/publications/105018398103#tab=citedBy
U2 - 10.1017/S0033291725102018
DO - 10.1017/S0033291725102018
M3 - Article
C2 - 41070707
AN - SCOPUS:105018398103
SN - 0033-2917
VL - 55
JO - Psychological Medicine
JF - Psychological Medicine
M1 - e307
ER -