试验报告:使用密度计和 NIDEK GS-1 球镜对青光眼患者的小梁网状结构色素进行客观量化

D. Laroche, Aaron Brown, José Sinon, Alexander Martin, Chester Ng, Sohail Sakkari
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引用次数: 0

摘要

在这个病例系列中,我们提出了一种方法,用于证明色素性青光眼独特生物标志物的开发原理,以检测神经纤维层脱失之前的进展情况。在该病例系列的五名患者中,有一名患者因小梁网色素过度浓密的假性外膜剥脱综合征而被排除在外。其余患者的视野缺损减少,上小梁网与下小梁网的比率增加。这种方法虽然因样本量较小而受到限制,但它表明,在少数患者中,视野缺损与上小梁网与下小梁网比率的增加呈正相关。下一步将研究无青光眼患者和色素性青光眼患者,同时对单侧剥脱综合征患者进行完整的眼间比较,以作为对照。据我们所知,这是一种新颖的方法,如果这种模式成立,它就可以作为开发色素性青光眼新型早期生物标志物的原理证明,以改善早期干预和延缓视力丧失。
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Pilot report: objective quantification of trabecular meshwork pigmentation using densitometry and the NIDEK GS-1 gonioscope in glaucoma patients
In this case series, we present a methodology for a proof of principle for the development of a unique biomarker for pigmentary glaucoma to detect progression before nerve fiber layer loss. Out of the five patients in this case series, one was excluded because of an outlier due to pseudoexfoliation syndrome with excessively dense pigmentation of the trabecular meshwork. The remaining patients displayed a decreased visual field loss with increased superior to inferior trabecular meshwork ratios. This methodology, though limited due to small sample size, shows that in a limited number of patients, visual field loss is positively correlated with increased superior to inferior trabecular meshwork ratios. The next steps would be to look at patients without glaucoma and patients with pigmentary glaucoma, along with complete inter-eye comparisons for patients with unilateral exfoliation syndrome to act as controls. To our knowledge, this is a novel methodology, and if the pattern holds, it can act as proof of principle for the development of a novel early biomarker for pigmentary glaucoma to improve early intervention and delay vision loss.
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