Xiaoyu Zhou, Yixin Hu, Jing Yang, Yao Huang, Hua Lan, Jiahui Zheng, Lin Tang, Jing Zhang, Jun Chen, Ting Yin, Daihong Liu, Jiuquan Zhang
{"title":"Glymphatic, Structural, and Cognitive Changes During Breast Cancer Chemotherapy: A Longitudinal MRI Study","authors":"Xiaoyu Zhou, Yixin Hu, Jing Yang, Yao Huang, Hua Lan, Jiahui Zheng, Lin Tang, Jing Zhang, Jun Chen, Ting Yin, Daihong Liu, Jiuquan Zhang","doi":"10.1002/hbm.70334","DOIUrl":null,"url":null,"abstract":"<p>The glymphatic system maintains brain homeostasis through cerebrospinal fluid transport and waste clearance. Its potential involvement in chemotherapy-related cognitive impairment remains largely unexplored due to limited in vivo evidence. In this prospective longitudinal study, 126 female breast cancer patients underwent multiparametric brain MRI and neuropsychological assessments at three time points: baseline (<span>bc</span>1), after the first cycle of neoadjuvant chemotherapy (<span>bc</span>2), and upon completion of neoadjuvant chemotherapy (<span>bc</span>3). Glymphatic function was assessed using four MRI-derived metrics: choroid plexus (CP) volume, perivascular space (PVS) volume fraction, free water (FW), and Diffusion Tensor Imaging–Along the Perivascular Space (DTI-ALPS) index. Brain tissue segmentation was conducted to quantify the volume fractions of gray matter (GM) in cortex and subcortex, white matter (WM), and cerebrospinal fluid (CSF) relative to intracranial volume. Neuropsychological assessments included the Self-Rating Anxiety Scale (SAS), the Functional Assessment of Cancer Therapy–Cognitive Function (FACT-Cog), and a battery of objective cognitive tests. Longitudinal changes and interrelationships were analyzed using linear mixed-effects models, correlation analyses, and cross-lagged panel analysis. During chemotherapy, CP volume increased (<i>p</i> < 0.001), while PVS volume fraction decreased (<i>p</i> = 0.003); no significant changes were found in FW or DTI-ALPS. GM volumes in both cortex and subcortex declined (both <i>p</i> = 0.02). SAS scores increased (<i>p</i> = 0.02), and FACT-Cog scores decreased (<i>p</i> < 0.001), with no significant changes in objective test scores. From <span>bc</span>2 to <span>bc</span>3, increases in CP volume were negatively correlated with reductions in PVS volume fraction (<i>r</i> = −0.40, <i>p</i> < 0.001). From <span>bc</span>1 to <span>bc</span>3, reductions in PVS volume fraction were associated with decreases in both cortical GM volumes (<i>r</i> = 0.32, <i>p</i> < 0.001). At <span>bc</span>2, cortical GM atrophy was correlated with increased SAS scores (<i>r</i> = −0.30, <i>p</i> = 0.002). Cross-lagged panel analysis showed that CP enlargement at <span>bc</span>2 preceded PVS volume fraction reduction at <span>bc</span>3 (<i>β</i> = −1.66, <i>p</i> = 0.007). During neoadjuvant chemotherapy, breast cancer patients exhibited a unique pattern of glymphatic system alterations, suggesting its potential as an imaging marker of treatment-related brain changes.</p>","PeriodicalId":13019,"journal":{"name":"Human Brain Mapping","volume":"46 13","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/hbm.70334","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Brain Mapping","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/hbm.70334","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROIMAGING","Score":null,"Total":0}
引用次数: 0
Abstract
The glymphatic system maintains brain homeostasis through cerebrospinal fluid transport and waste clearance. Its potential involvement in chemotherapy-related cognitive impairment remains largely unexplored due to limited in vivo evidence. In this prospective longitudinal study, 126 female breast cancer patients underwent multiparametric brain MRI and neuropsychological assessments at three time points: baseline (bc1), after the first cycle of neoadjuvant chemotherapy (bc2), and upon completion of neoadjuvant chemotherapy (bc3). Glymphatic function was assessed using four MRI-derived metrics: choroid plexus (CP) volume, perivascular space (PVS) volume fraction, free water (FW), and Diffusion Tensor Imaging–Along the Perivascular Space (DTI-ALPS) index. Brain tissue segmentation was conducted to quantify the volume fractions of gray matter (GM) in cortex and subcortex, white matter (WM), and cerebrospinal fluid (CSF) relative to intracranial volume. Neuropsychological assessments included the Self-Rating Anxiety Scale (SAS), the Functional Assessment of Cancer Therapy–Cognitive Function (FACT-Cog), and a battery of objective cognitive tests. Longitudinal changes and interrelationships were analyzed using linear mixed-effects models, correlation analyses, and cross-lagged panel analysis. During chemotherapy, CP volume increased (p < 0.001), while PVS volume fraction decreased (p = 0.003); no significant changes were found in FW or DTI-ALPS. GM volumes in both cortex and subcortex declined (both p = 0.02). SAS scores increased (p = 0.02), and FACT-Cog scores decreased (p < 0.001), with no significant changes in objective test scores. From bc2 to bc3, increases in CP volume were negatively correlated with reductions in PVS volume fraction (r = −0.40, p < 0.001). From bc1 to bc3, reductions in PVS volume fraction were associated with decreases in both cortical GM volumes (r = 0.32, p < 0.001). At bc2, cortical GM atrophy was correlated with increased SAS scores (r = −0.30, p = 0.002). Cross-lagged panel analysis showed that CP enlargement at bc2 preceded PVS volume fraction reduction at bc3 (β = −1.66, p = 0.007). During neoadjuvant chemotherapy, breast cancer patients exhibited a unique pattern of glymphatic system alterations, suggesting its potential as an imaging marker of treatment-related brain changes.
期刊介绍:
Human Brain Mapping publishes peer-reviewed basic, clinical, technical, and theoretical research in the interdisciplinary and rapidly expanding field of human brain mapping. The journal features research derived from non-invasive brain imaging modalities used to explore the spatial and temporal organization of the neural systems supporting human behavior. Imaging modalities of interest include positron emission tomography, event-related potentials, electro-and magnetoencephalography, magnetic resonance imaging, and single-photon emission tomography. Brain mapping research in both normal and clinical populations is encouraged.
Article formats include Research Articles, Review Articles, Clinical Case Studies, and Technique, as well as Technological Developments, Theoretical Articles, and Synthetic Reviews. Technical advances, such as novel brain imaging methods, analyses for detecting or localizing neural activity, synergistic uses of multiple imaging modalities, and strategies for the design of behavioral paradigms and neural-systems modeling are of particular interest. The journal endorses the propagation of methodological standards and encourages database development in the field of human brain mapping.