Tian-Ye Lin , Shao-Shuai Sun , Yang Yang , Qing-Yang Li , Nan Sun , Ying-Shi Sun
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引用次数: 0
Abstract
Background
Anxiety sensitivity (AS) significantly impacts treatment outcomes and quality of life in breast cancer patients, yet the neural mechanisms underlying AS-related brain structural changes remain poorly understood.
Aims
To investigate brain structural alterations associated with AS and their temporal evolution in patients with breast cancer.
Methods
Eighty-five patients with breast cancer (42 with high AS and 43 with low AS) and 42 healthy controls (HCs) were recruited. Voxel-based morphometry analysis was conducted to examine gray matter volume (GMV) differences between the high and low AS patient groups and the HCs. Causal structural covariance network (CaSCN) analysis was employed to investigate the inferred temporal evolution of GMV alterations in relation to AS levels and disease duration using cross-sectional data.
Results
AS levels showed a marked decline within the first two months post-diagnosis before stabilizing. Both patient groups exhibited GMV reduction compared with HCs, with low AS patients showing more widespread atrophy. The left middle cingulum (MCC.L) GMV negatively correlated with AS scores in high AS patients (r = −0.448, P = 0.0029). CaSCN analysis revealed a directional influence pathway from the MCC.L to the right thalamus (THA.R), with the THA.R showing positive self-feedback. Conjunction analysis identified shared effects of decreasing AS and increasing illness duration mediated by the THA.R, resulting in concordant atrophy in regions such as the left cerebellum (lobule VI) and discordant changes in temporal, parietal, and limbic areas.
Conclusions
THA.R plays a central role in mediating AS-related brain structural alterations in breast cancer patients, offering potential therapeutic targets for managing AS.
期刊介绍:
The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.