通过玻璃体钆造影剂MR成像的眼溶质运动方向和颅内清除:作为淋巴功能障碍的新生物标志物的潜力。

IF 3.2
Shinji Naganawa, Rintaro Ito, Mariko Kawamura, Toshiaki Taoka, Tadao Yoshida, Michihiko Sone
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引用次数: 0

摘要

目的:眼淋巴系统和脑淋巴系统可能有共同的生理通路。我们假设泄漏到玻璃体中的钆基造影剂(GBCA)的前后运动可以作为脑淋巴功能的生物标志物。本研究旨在回顾性探讨MRI上玻璃体内GBCA分布与最近提出的脑废物清除受损成像标志物之间的关系。方法:我们分析了78名成年参与者的156只眼睛,他们在给予标准剂量GBCA后4小时接受了3T MRI检查。在3D-real IR图像上,我们计算了“对比度偏移指数”(感兴趣的玻璃体前后体积之间的信号差异:VOIa-VOIp)来量化前后GBCA分布。主要终点是乙状窦后脑膜淋巴管(PML-PSS)或基底节区血管周围间隙增强(PVS-BG)阳性的复合终点。采用聚类稳健推理的多变量逻辑回归来评估预测因素,包括对比度偏移指数、平均玻璃体对比度分布、年龄、性别和眼轴长度。结果:表明GBCA优先前路分布的对比移位指数阳性与脑清除率受损的综合结果有显著且独立的相关性(P = 0.006)。结论:玻璃体中GBCA的正向分布是一种新的、无创的与脑清除功能受损相关的成像生物标志物。这种“对比移位指数”可能反映了眼睛和大脑中常见的全身性淋巴失调,为评估神经退行性风险提供了一种新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ocular Solute Movement Direction and Intracranial Clearance via Vitreous Gadolinium-based Contrast Agent MR Imaging: Potential as a Novel Biomarker for Glymphatic Dysfunction.

Purpose: The ocular and brain glymphatic systems may share common physiological pathways. We hypothesized that the anteroposterior movement of gadolinium-based contrast agent (GBCA) that has leaked into the vitreous could serve as a biomarker for brain glymphatic function. This study aimed to retrospectively investigate the association between the intravitreal GBCA distribution on MRI and recently proposed imaging markers of impaired brain waste clearance.

Methods: We analyzed 156 eyes from 78 adult participants who underwent 3T MRI 4 hr after standard-dose GBCA administration. On 3D-real IR images, we calculated a "contrast shift index" (the signal difference between anterior and posterior vitreous volumes of interest: VOIa-VOIp) to quantify the anteroposterior GBCA distribution. The primary outcome was a composite endpoint of positivity for either putative meningeal lymphatics at the posterior sigmoid sinus (PML-PSS) or enhanced basal ganglia perivascular spaces (PVS-BG). Multivariable logistic regression with cluster-robust inference was used to assess predictors, including the contrast shift index, mean vitreous contrast distribution, age, sex, and axial length of the eye.

Results: A positive contrast shift index, indicating preferential anterior GBCA distribution, was significantly and independently associated with the composite outcome of impaired brain clearance (P = 0.006). Age (P <0.001) and male sex (P = 0.009) were also independent predictors. A predictive model incorporating these factors demonstrated high discrimination, with an area under the receiver operating characteristic curve (AUC) of 0.872. Axial length of the eye and mean vitreous contrast distribution were not significant independent predictors.

Conclusion: The anteroposterior distribution of GBCA in the vitreous is a novel, non-invasive imaging biomarker associated with impaired brain clearance function. This "contrast shift index" may reflect systemic glymphatic dysregulation common to both the eye and brain, offering a new avenue for assessing neurodegenerative risk.

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