1.5T MR成像对青光眼神经退行性病变眼-视通路完整性的临床评价:青光眼神经退行性病变的完整性

Engin Kaya N, Yiğit Ulviye, Bayramoğlu Sibel Töreyen, Güner Nurten Turan, Özyurt Onur, Tufan Kutlay, Ağaçhan Ahmet, Çağatay Penbe
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摘要

目的:越来越多的数据表明青光眼可能是一种影响整个视觉系统的神经退行性疾病。我们利用1.5T弥散张量磁共振成像技术评估了球后青光眼的损伤,并将这些技术与大量病例的临床数据进行了比较。材料与方法:本横断面研究纳入65例原发性开角型青光眼患者130只眼。选择无已知眼部或全身伴发疾病、神经系统疾病、既往青光眼手术或抗氧化剂使用的患者。视神经束造影观察到严重青光眼不对称受累患者的视神经厚度减少和扩散恶化。记录受试者的光学相干层析成像和视野结果。记录青光眼光学相干层析分析和标准自动视距测量结果。对视神经和辐射进行扩散张量磁共振成像分析,计算分数各向异性、表观扩散系数、轴向扩散系数和径向扩散系数。统计学评价扩散张量磁共振成像与青光眼神经变性患者临床眼参数的相关性。结果:扩散参数与年龄呈极显著相关。神经节细胞复合体与视神经的表观扩散系数、轴向和径向扩散系数有统计学意义。结论:青光眼的眼脑连接可通过常规临床仪器进行评估。我们的研究也揭示了球后青光眼神经变性与眼部损伤的有限相关性。更好地了解球后损伤将使我们能够制定更有效的策略和更准确地了解青光眼。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical evaluation of the eye-to-visual-pathway integrity of glaucomatous neurodegeneration using 1.5T MR imaging: The integrity of glaucomatous neurodegeneration
Aim: Accumulating data imply that glaucoma may represent a neurodegenerative disorder affecting the entire visual system. We evaluated retrobulbar glaucomatous damage with favorable techniques for 1.5T diffusion-tensor magnetic resonance imaging and we compared those techniques with clinical data in a large case series. Material and methods: This Cross-sectional study included 130 eyes of 65 patients with primary open-angle glaucoma. Patients with no known ocular or systemic concomitant disorders, neurological diseases, previous glaucoma surgeries, or antioxidant usage were selected. A decrease in thickness and deterioration in the optic nerve diffusion of severely glaucomatous eyes of patients with asymmetrical involvement was observed in optic nerve tractography. Optical coherence tomography and visual field results of the subjects were recorded. Glaucoma analysis with optical coherence tomography and standard automated perimetry results of the subjects were recorded. Diffusion-tensor magnetic resonance imaging analysis of optic nerves and radiations were performed, computing fractional anisotropy, apparent diffusion coefficient, axial diffusivity, and radial diffusivity. Correlation between the diffusion-tensor magnetic resonance imaging and clinical eye parameters of glaucomatous neurodegeneration were statistically evaluated. Results: The correlations between diffusion parameters and age were highly significant. Statistically significant correlations were found between ganglion cell complex and apparent diffusion coefficient, axial and radial diffusivities of optic nerves. Conclusion: Eye-brain connection in glaucoma can be evaluated with routine clinical instruments. Our study also revealed a limited correlation of retrobulbar glaucomatous neurodegeneration with ophthalmic damage. A better understanding of retrobulbar damage will enable us to develop more efficient strategies and a more accurate understanding of glaucoma.
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