Medical Retina and Visual Science Laboratories, Institute of Health and Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Brisbane, QLD, 4059, Australia.
School of Optometry and Vision Science, Queensland University of Technology, Brisbane, QLD, Australia.
Sci Rep. 2016 Sep 13;6:33373. doi: 10.1038/srep33373.
It is difficult to detect visual function deficits in patients at risk for glaucoma (glaucoma suspects) and at early disease stages with conventional ophthalmic tests such as perimetry. To this end, we introduce a novel quadrant field measure of the melanopsin retinal ganglion cell mediated pupil light response corresponding with typical glaucomatous arcuate visual field defects. The melanopsin-mediated post-illumination pupil response (PIPR) was measured in 46 patients with different stages of glaucoma including glaucoma suspects and compared to a healthy group of 21 participants with no disease. We demonstrate that the superonasal quadrant PIPR differentiated glaucoma suspects and early glaucoma patients from controls with fair (AUC = 0.74) and excellent (AUC = 0.94) diagnostic accuracy, respectively. The superonasal PIPR provides a linear functional correlate of structural retinal nerve fibre thinning in glaucoma suspects and early glaucoma patients. This first report that quadrant PIPR stimulation detects melanopsin dysfunction in patients with early glaucoma and at pre-perimetric stages may have future implications in treatment decisions of glaucoma suspects.
用传统的眼科测试(如视野检查)很难检测出青光眼高危患者(青光眼疑似患者)和早期患者的视觉功能缺陷。为此,我们引入了一种新的象限视野测量方法,用于测量黑素细胞视蛋白介导的瞳孔光反应,该反应与典型的青光眼弓形视野缺损相对应。在包括青光眼疑似患者和不同阶段青光眼患者在内的 46 名患者以及 21 名无疾病的健康对照组中测量了黑素细胞视蛋白介导的光照后瞳孔反应(PIPR)。我们证明,超鼻上象限的 PIPR 可以分别以中等(AUC=0.74)和优异(AUC=0.94)的诊断准确性区分青光眼疑似患者和早期青光眼患者与对照组。超鼻上象限的 PIPR 提供了青光眼疑似患者和早期青光眼患者中结构视网膜神经纤维变薄的线性功能相关性。这是首次报道象限 PIPR 刺激可检测出早期青光眼和亚临床阶段患者的黑素细胞视蛋白功能障碍,这可能对青光眼疑似患者的治疗决策产生未来影响。