Alterations in degree centrality and cognitive function in breast cancer patients after chemotherapy

被引:3
作者
Zhou, Wensu [1 ]
Tian, Weizhong [2 ]
Xia, Jianguo [2 ]
Li, Yuan [2 ]
Li, Xiaolu [1 ]
Yao, Tianyi [3 ]
Bi, Jingcheng [3 ]
Zhu, Zhengcai [3 ]
机构
[1] Dalian Med Univ, Grad Sch, Dalian 116044, Peoples R China
[2] Taizhou Peoples Hosp, Dept Radiol, Taizhou 225300, Jiangsu, Peoples R China
[3] Taizhou Peoples Hosp, Dept Breast & Thyroid Surg, Taizhou 225300, Jiangsu, Peoples R China
关键词
Breast cancer; Chemo brain; Cognitive function; Degree centrality; fMRI; IMPAIRMENT;
D O I
10.1007/s11682-022-00695-w
中图分类号
R445 [影像诊断学];
学科分类号
100207 ;
摘要
The goal of this study was to determine the presence or absence of persistent functional impairments in specific brain regions in breast cancer patients during the recovery period after chemotherapy. We calculated degree centrality (DC) and explored the correlation between brain changes and cognitive scores in 29 female patients with breast cancer who had completed chemotherapy within 1-6 years (C + group) and in 28 age-matched patients with breast cancer who did not receive chemotherapy (C- group). All patients underwent rs-fMRI and cognitive testing. Differences in brain functional activity were explored using DC parameters. Correlations between brain features and cognitive scores were analyzed via correlation analysis. Compared with the C- group, the C + group obtained significantly lower motor and cognitive subscores on the Fatigue Scale for Motor and Cognitive Functions and four subscale scores of the Functional Assessment of Cancer Therapy-Cognitive Function (P < 0.05). Furthermore, the C + group exhibited a significantly higher DC z-score (zDC) in the right superior temporal gyrus and left postcentral gyrus (P < 0.01, FWE-corrected), and a lower zDC in the left caudate nucleus (P < 0.01, FWE-corrected). We found a positive correlation between digit symbol test (DST) scores and zDC values in the right superior temporal gyrus (r = 0.709, P < 0.001), and a negative correlation between DST scores and zDC values in the right angular gyrus (r = -0.784, P < 0.001) and left superior parietal gyrus (r = -0.739, P < 0.001). Chemotherapy can cause abnormal brain activity and cognitive decline in patients with breast cancer, and these effects are likely to persist. DC can be used as an imaging marker for chemotherapy-related cognitive impairment after chemotherapy in breast cancer patients.
引用
收藏
页码:2248 / 2257
页数:10
相关论文
共 36 条
[31]   Functional neuroimaging in subjective cognitive decline: current status and a research path forward [J].
Viviano, Raymond P. ;
Damoiseaux, Jessica S. .
ALZHEIMERS RESEARCH & THERAPY, 2020, 12 (01)
[32]   Multisensory Integration as a Window into Orderly and Disrupted Cognition and Communication [J].
Wallace, Mark T. ;
Woynaroski, Tiffany G. ;
Stevenson, Ryan A. .
ANNUAL REVIEW OF PSYCHOLOGY, VOL 71, 2020, 71 :193-219
[33]   Altered Brain Network Centrality in Patients with Adult Strabismus with Amblyopia: A Resting-State Functional Magnetic Resonance Imaging (fMRI) Study [J].
Wu, Kang-Rui ;
Yu, Ya-Jie ;
Tang, Li-Ying ;
Chen, Si-Yi ;
Zhang, Meng-Yao ;
Sun, Tie ;
Wu, Shi-Nan ;
Yu, Kang ;
Li, Biao ;
Shao, Yi .
MEDICAL SCIENCE MONITOR, 2020, 26
[34]   Alterations of Functional Connectivity in Stroke Patients With Basal Ganglia Damage and Cognitive Impairment [J].
Yao, Guanqun ;
Li, Jing ;
Liu, Sha ;
Wang, Jiaojian ;
Cao, Xiaohua ;
Li, Xinrong ;
Cheng, Long ;
Chen, Huafu ;
Xu, Yong .
FRONTIERS IN NEUROLOGY, 2020, 11
[35]   Changes of Regional Neural Activity Homogeneity in Preclinical Alzheimer's Disease: Compensation and Dysfunction [J].
Zhang, Zhen ;
Cui, Liang ;
Huang, Yanlu ;
Chen, Yu ;
Li, Yuehua ;
Guo, Qihao .
FRONTIERS IN NEUROSCIENCE, 2021, 15
[36]   Differences in verbal memory retrieval in breast cancer chemotherapy patients compared to healthy controls: a prospective fMRI study [J].
Zunini, Rocio A. Lopez ;
Scherling, Carole ;
Wallis, Nancy ;
Collins, Barbara ;
MacKenzie, Joyce ;
Bielajew, Catherine ;
Smith, Andra M. .
BRAIN IMAGING AND BEHAVIOR, 2013, 7 (04) :460-477