ARC Centre of Excellence in Vision Science, The John Curtin School of Medical Research, The Australian National University, Canberra City, ACT, Australia.
Invest Ophthalmol Vis Sci. 2013 Jan 17;54(1):467-75. doi: 10.1167/iovs.12-10829.
We are developing multifocal pupillographic objective perimetry (mfPOP) to assess localized changes in function within visual pathways. In this study, we investigate novel mfPOP stimuli designed to target neural components from either or both the sub-cortical pupillary luminance response and the cortically driven color response.
Pupillary responses of 12 subjects were recorded to eight mfPOP stimulus variants (protocols). Forty-eight visual field test-regions (24/eye) were stimulated concurrently with uncorrelated sequences of either high or low luminance-contrast, luminance- plus color-contrast, or equiluminant color-exchange stimuli. Stimulus pulses were of 50 ms duration and were presented at mean intervals of 4 seconds/region. Test durations were 4 or 8 minutes; therefore, estimated responses were derived from 60 or 120 stimulus presentations to each test region.
Pupillary response amplitudes were more influenced by luminance-contrast than the color-contrast of stimuli; response delays, however, were more closely linked to the proportion of color- versus luminance-contrast in each protocol. Significant differences (P < 0.05) in amplitudes but not delays were present between all three high luminance-contrast protocols and a low luminance-contrast luminance protocol, regardless of color content. The reverse pattern was observed between the equiluminant color exchange protocol and this same low luminance-contrast luminance protocol. Only the low luminance-contrast plus color exchange protocol differed significantly from the low luminance-contrast luminance protocol in both measures.
Two protocols, utilizing low and high luminance-contrast plus color exchange, were identified as likely to incorporate both cortical and subcortical response components, and were deemed potential candidates for further investigation in clinical studies.
我们正在开发多焦瞳孔客观视野计(mfPOP),以评估视觉通路中功能的局部变化。在这项研究中,我们研究了旨在针对来自皮质驱动的颜色反应和皮质下瞳孔亮度反应的神经成分的新型 mfPOP 刺激。
记录了 12 名受试者的瞳孔反应,以记录八种 mfPOP 刺激变体(方案)。四十八个视野测试区域(每只眼 24 个)同时用不相关的高或低亮度对比度、亮度加颜色对比度或等亮度颜色交换刺激序列刺激。刺激脉冲持续 50ms,每个区域的平均间隔为 4 秒/脉冲。测试持续时间为 4 或 8 分钟;因此,每个测试区域的估计响应来自 60 或 120 次刺激呈现。
瞳孔反应幅度受刺激的亮度对比度影响较大,而受颜色对比度影响较小;然而,反应延迟与每个方案中颜色与亮度对比度的比例更密切相关。所有三种高亮度对比度方案与低亮度对比度亮度方案之间的幅度(但不是延迟)均存在显著差异(P <0.05),无论颜色内容如何。在相同的低亮度对比度亮度方案中,等亮度颜色交换方案与该方案之间观察到相反的模式。只有低亮度对比度加颜色交换方案在这两个测量中与低亮度对比度亮度方案有显著差异。
两种方案,利用低和高亮度对比度加颜色交换,被认为可能包含皮质和皮质下反应成分,是进一步在临床研究中进行调查的潜在候选方案。