通过多参数磁共振成像评估脑肿瘤淋巴功能的组织病理学相关性研究

IF 10 1区 医学 Q1 ONCOLOGY
Min Gao, Zhengliang Liu, Hongjing Zang, Xiong Wu, Yizhong Yan, Hai Lin, Jianmin Yuan, Tianming Liu, Yu Zhou, Jun Liu
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引用次数: 0

摘要

目的:本研究旨在阐明脑肿瘤对脑水肿和脑水肿引流的影响,利用先进的成像技术探讨肿瘤特征、脑水肿功能和水通道蛋白4(AQP4)表达之间的关系:在 2022 年 3 月至 2023 年 4 月的前瞻性队列中,胶质母细胞瘤、脑转移瘤和侵袭性脑膜瘤患者与年龄和性别匹配的健康对照组一起接受了 3.0T 磁共振成像,包括沿血管周围空间的弥散张量成像分析(DTI-ALPS)指数和用于定量脑图谱的多参数磁共振成像(MTP)。通过免疫荧光分析肿瘤和肿瘤周围组织的 AQP4 表达。对成像参数、脑功能(DTI-ALPS 指数)和 AQP4 表达之间的相关性进行了统计学评估:结果:在 84 名患者(平均年龄:55 ± 12 岁;38 名男性)和 59 名对照组患者(平均年龄:54 ± 8 岁;23 名男性)中,脑肿瘤患者的血流功能明显降低(DTI-ALPS 指数:2.315 vs. 2.879;p = 0.001),脑脊液(CSF)体积增加(201.376 cm³ vs. 115.957 cm³;p = 0.001)。肿瘤体积与DTI-ALPS指数呈负相关(r:-0.715,p<0.001),而AQP4的表达与瘤周脑水肿(PTBE)体积呈正相关(r:0.989;p<0.001),与PTBE区域的PD呈负相关(ρ:-0.506;p<0.001):我们的研究结果突显了肿瘤诱导的压迫、淋巴功能障碍和液体动力学改变之间的相互作用,显示了 DTI-ALPS 和 MTP 在理解肿瘤相关脑水肿的病理生理学方面的实用性。这些见解为进一步对甘液系统进行神经肿瘤学研究奠定了放射学基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Histopathologic Correlation Study Evaluating Glymphatic Function in Brain Tumors by Multiparametric MRI.

Purpose: This study aimed to elucidate the impact of brain tumors on cerebral edema and glymphatic drainage by leveraging advanced MRI techniques to explore the relationships among tumor characteristics, glymphatic function, and aquaporin-4 (AQP4) expression levels.

Experimental design: In a prospective cohort from March 2022 to April 2023, patients with glioblastoma, brain metastases, and aggressive meningiomas, alongside age- and sex-matched healthy controls, underwent 3.0T MRI, including diffusion tensor imaging analysis along the perivascular space (DTI-ALPS) index and multiparametric MRI for quantitative brain mapping. Tumor and peritumor tissues were analyzed for AQP4 expression levels via immunofluorescence. Correlations among MRI parameters, glymphatic function (DTI-ALPS index), and AQP4 expression levels were statistically assessed.

Results: Among 84 patients (mean age: 55 ± 12 years; 38 males) and 59 controls (mean age: 54 ± 8 years; 23 males), patients with brain tumor exhibited significantly reduced glymphatic function (DTI-ALPS index: 2.315 vs. 2.879; P = 0.001) and increased cerebrospinal fluid volume (201.376 cm³ vs. 115.957 cm³; P = 0.001). A negative correlation was observed between tumor volume and the DTI-ALPS index (r: -0.715, P < 0.001), whereas AQP4 expression levels correlated positively with peritumoral brain edema volume (r: 0.989, P < 0.001) and negatively with proton density in peritumoral brain edema areas (ρ: -0.506, P < 0.001).

Conclusions: Our findings highlight the interplay among tumor-induced compression, glymphatic dysfunction, and altered fluid dynamics, demonstrating the utility of DTI-ALPS and multiparametric MRI in understanding the pathophysiology of tumor-related cerebral edema. These insights provide a radiological foundation for further neuro-oncological investigations into the glymphatic system. See related commentary by Surov and Borggrefe, p. 4813.

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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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