乳腺癌化疗期间淋巴、结构和认知的改变:一项纵向MRI研究

IF 3.3 2区 医学 Q1 NEUROIMAGING
Xiaoyu Zhou, Yixin Hu, Jing Yang, Yao Huang, Hua Lan, Jiahui Zheng, Lin Tang, Jing Zhang, Jun Chen, Ting Yin, Daihong Liu, Jiuquan Zhang
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引用次数: 0

摘要

淋巴系统通过脑脊液运输和废物清除维持脑内稳态。由于体内证据有限,其在化疗相关认知障碍中的潜在作用仍未得到充分研究。在这项前瞻性纵向研究中,126名女性乳腺癌患者在三个时间点接受了多参数脑MRI和神经心理学评估:基线(bc1),新辅助化疗第一周期后(bc2),新辅助化疗完成后(bc3)。使用四个mri衍生指标评估淋巴功能:脉络膜丛(CP)体积、血管周围空间(PVS)体积分数、游离水(FW)和沿血管周围空间扩散张量成像(DTI-ALPS)指数。进行脑组织分割,量化皮层和皮层下灰质(GM)、白质(WM)和脑脊液(CSF)相对于颅内体积的体积分数。神经心理学评估包括焦虑自评量表(SAS)、癌症治疗-认知功能功能评估(FACT-Cog)和一系列客观认知测试。使用线性混合效应模型、相关分析和交叉滞后面板分析分析纵向变化和相互关系。化疗期间,CP体积增加(p < 0.001), PVS体积分数降低(p = 0.003);FW和DTI-ALPS均未见明显变化。皮层和皮层下GM体积均下降(p = 0.02)。SAS得分上升(p = 0.02), FACT-Cog得分下降(p < 0.001),客观测试得分无显著变化。从bc2到bc3, CP体积的增加与PVS体积分数的降低呈负相关(r = - 0.40, p < 0.001)。从bc1到bc3, PVS体积分数的降低与皮质GM体积的降低相关(r = 0.32, p < 0.001)。在bc2时,皮质GM萎缩与SAS评分升高相关(r = - 0.30, p = 0.002)。交叉滞后面板分析显示,bc2时CP增大先于bc3时pv体积分数降低(β = - 1.66, p = 0.007)。在新辅助化疗期间,乳腺癌患者表现出一种独特的淋巴系统改变模式,这表明它有可能作为治疗相关脑变化的影像学标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

Glymphatic, Structural, and Cognitive Changes During Breast Cancer Chemotherapy: A Longitudinal MRI 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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来源期刊
Human Brain Mapping
Human Brain Mapping 医学-核医学
CiteScore
8.30
自引率
6.20%
发文量
401
审稿时长
3-6 weeks
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.
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