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Brain structure & function · 2026

Functional Breakdown of Temporoparietal Junction Interaction in High-depression Individuals: Evidence from Multi-Metric Connectomics.

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Wen Xiaotong, Fengge Yao, Han Bin, Wei Guodong, Gao Yuehan, Chen Yuying, Hao Ziyu, Li Huanhuan, Dou Fengyu

Аннотация

Depression involves impaired cognitive, affective, and social functions associated with aberrant brain network interactions. The temporoparietal junction (TPJ), a multisensory integration hub, exhibits depression-related connectivity alterations, yet the roles of its subregions during subclinical stages remain unclear. This study examined TPJ subregional communication in non-clinical high-depression individuals. Resting-state fMRI data from 586 medication-free young adults were analyzed. Participants were divided into high-depression (HD, N = 130) and low-depression (LD, N = 130) groups using Beck Depression Inventory scores. TPJ was parcellated into anterior (aTPJ), posterior (pTPJ), and ventral (vTPJ) subregions via community detection. Multi-metric connectivity (functional connectivity/FC, total interdependence/TI, Granger causality/GC) seeded from TPJ subregions was compared between groups. Support vector machine (SVM) fusion analysis identified high-contribution features for network alteration modeling. TPJ subregions showed depression-related connectivity patterns: (1) Altered default mode network DMN interactions featuring enhanced anterior DMN (medial prefrontal cortex) connectivity and weakened posterior DMN (posterior cingulate/precuneus) connectivity; (2) Disrupted left TPJ-reward pathway communication (ventral striatum, putamen, amygdala); (3) Right TPJ/left vTPJ hyperconnectivity with cognitive control systems (frontoparietal network, orbitofrontal cortex, anterior cingulate cortex); (4) Enhanced somatosensory-motor connectivity with reduced visual/auditory input; (5) Impaired intra-TPJ communication. TPJ subregions exhibit distinct dysconnectivity patterns in non-clinical depression, affecting self-referential processing, reward integration, and cognitive control. Multi-metric profiling identifies TPJ as a potential pathophysiological biomarker.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты