Glymphatic, Structural, and Cognitive Changes During Breast Cancer Chemotherapy: A Longitudinal <scp>MRI</scp> Study

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.

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Publication Details

Journal
Human Brain Mapping
Published
2025-08-29
DOI
https://doi.org/10.1002/hbm.70334
Citations
2
Primary Topic
Cancer-related cognitive impairment studies
Type
article
Field-Weighted Citation Impact
3.04

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article

Glymphatic, Structural, and Cognitive Changes During Breast Cancer Chemotherapy: A Longitudinal MRI Study

Jing Zhang, Ting Yin, Jiuquan Zhang, Jing Yang et al.
2 citations
Human Brain Mapping
Cancer-related cognitive impairment studies
3.04
article

Glymphatic, Structural, and Cognitive Changes During Breast Cancer Chemotherapy: A Longitudinal MRI Study

Jing Zhang, Ting Yin, Jiuquan Zhang, Jing Yang, Jun Chen, Lin Tang, Yixin Hu, Xiaoyu Zhou, Yao Huang, Daihong Liu, Jiahui Zheng, Lan Hua
article en
2 citations

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.

Human Brain MappingVol. 46(13)
Bayer (United States) (US), Chongqing University (CN), Siemens Healthcare (United States) (US), Chongqing Cancer Hospital (CN)
National Natural Science Foundation of China, Centre Scientifique et Technique du Bâtiment, Research and Innovation Foundation
Openalex Percentile: Top 8%
Cancer-related cognitive impairment studies
3.04
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