Journal of affective disorders · 2025
Cortical activation patterns in generalized anxiety and major depressive disorders measured by multi-channel near-infrared spectroscopy.
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Jialin Anfeirea, Zhang Hong-Guang, Wang Xiao-Hui, Wang Jia-Feng, Zhao Xin-Ying, Wang Chu, Cao Min-Ne, Li Xiao-Jing, Li Yue, Cao Lan-Lan, Zhong Bao-Liang, Deng Wei
Аннотация
BACKGROUND: Major depressive disorder (MDD) and generalized anxiety disorder (GAD) are highly prevalent mental disorders in psychiatry, but their overlapping symptoms often complicate precise diagnoses. This study aims to explore differential brain activation patterns in healthy controls (HC), MDD, and GAD groups through functional near-infrared spectroscopy (fNIRS) during the verbal fluency task (VFT) to enhance the accuracy of clinical diagnoses.
METHODS: This study recruited 30 patients with MDD, 45 patients with GAD, and 34 demographically matched HCs. Hemodynamic changes in the prefrontal cortex (PFC) and temporal lobes were measured using a 48-channel fNIRS during the VFT task. Demographics information, clinical characteristics and VFT performance were also recorded.
RESULTS: Compared to HCs, both MDD and GAD share a neurobiological phenotype of hypoactivation in the dorsolateral prefrontal cortex (DLPFC) and medial prefrontal cortex (mPFC) during VFT. Moreover, MDD patients exhibited significantly greater hypoactivation in the left DLPFC and mPFC than GAD patients.
CONCLUSIONS: Although both GAD and MDD patients exhibit disrupted cortical function, the impairment is less severe in GAD. These findings provide preliminary neurophysiological evidence supporting the utility of the fNIRS-VFT paradigm in differentiating GAD from MDD. This approach may complement traditional diagnostic methods, inform targeted interventions, and ultimately enhance patient outcomes.
METHODS: This study recruited 30 patients with MDD, 45 patients with GAD, and 34 demographically matched HCs. Hemodynamic changes in the prefrontal cortex (PFC) and temporal lobes were measured using a 48-channel fNIRS during the VFT task. Demographics information, clinical characteristics and VFT performance were also recorded.
RESULTS: Compared to HCs, both MDD and GAD share a neurobiological phenotype of hypoactivation in the dorsolateral prefrontal cortex (DLPFC) and medial prefrontal cortex (mPFC) during VFT. Moreover, MDD patients exhibited significantly greater hypoactivation in the left DLPFC and mPFC than GAD patients.
CONCLUSIONS: Although both GAD and MDD patients exhibit disrupted cortical function, the impairment is less severe in GAD. These findings provide preliminary neurophysiological evidence supporting the utility of the fNIRS-VFT paradigm in differentiating GAD from MDD. This approach may complement traditional diagnostic methods, inform targeted interventions, and ultimately enhance patient outcomes.