Pupillometric and perceptual approaches provide independent estimates of melanopsin activity in humans.

IF 5.6 2区 医学 Q1 Medicine
Sleep Pub Date : 2025-02-10 DOI:10.1093/sleep/zsae289
Tom Woelders, Altug Didikoglu, Lucien Bickerstaff, Timothy M Brown, Robert J Lucas
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引用次数: 0

Abstract

Study objectives: Melanopsin-expressing retinal ganglion cells, which provide light information to time sleep and entrain circadian clocks, also influence perceived brightness raising the possibility that psychophysical paradigms could be used to explore the origins and implications of variability in melanopic sensitivity. We aimed to develop accessible psychophysical tests of melanopic vision and relate outcomes with a pupillometric measure of melanopsin function (post-illumination pupil response) and prior light exposure.

Methods: Individually calibrated pairs of isoluminant stimuli differing in melanopic radiance from a four primary source were presented sequentially with superimposed random color offsets in a two alternative forced choice brightness preference paradigm to 41 naïve adult participants with personal light exposure data for the prior 7 days and post-illumination pupil response measures defined by comparing maintained pupil constriction for luminance matched "red" vs "blue" pulses.

Results: Across participants we observed the expected tendency to report positive melanopsin contrast stimuli as "brighter" (one-tailed t-test p < 0.001), but with substantial inter-individual variability in both sensitivity (melanopsin contrast at criterion preference p = 0.75) and amplitude (preference at maximum melanopic contrast). There was little correlation between these psychophysical outcomes and post-illumination pupil response magnitude, or between either psychophysical or post-illumination pupil response measures and light history metrics (pairwise Pearson correlation coefficients -0.5> < 0.5). Random forest machine learning failed to satisfactorily predict outcome for either psychophysical or post-illumination pupil response measures based upon these inputs.

Conclusions: Our findings reveal that estimates of melanopic function provided by perceptual and pupillometric paradigms can be largely independent of one another and of recent history of light exposure.

瞳孔测量和感知方法提供了人类黑视素活性的独立估计。
研究目的:表达黑视素的视网膜神经节细胞为睡眠时间和携带生物钟提供光信息,也影响感知亮度,这提高了心理物理范式可用于探索黑视敏感性变异的起源和含义的可能性。我们的目的是开发易于使用的黑视视觉的心理物理测试,并将结果与黑视素功能的瞳孔测量相关联(照明后瞳孔反应;PIPR)和先前的光照。方法:分别校准来自四个主要光源的不同黑视亮度的等亮度刺激对,并在两种可选的强制选择亮度偏好范式中依次叠加随机颜色偏移,向41名naïve成年参与者提供个人前7天的光照数据,并通过比较亮度匹配的“红色”与“蓝色”脉冲的瞳孔收缩来定义PIPR测量。结果:在所有参与者中,我们观察到报告阳性黑视素对比刺激为“更亮”的预期趋势(单尾t检验)。结论:我们的研究结果表明,由感知和瞳孔测量范式提供的黑视功能估计在很大程度上可以相互独立,并且与最近的光照史无关。
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来源期刊
Sleep
Sleep Medicine-Neurology (clinical)
CiteScore
8.70
自引率
10.70%
发文量
0
期刊介绍: SLEEP® publishes findings from studies conducted at any level of analysis, including: Genes Molecules Cells Physiology Neural systems and circuits Behavior and cognition Self-report SLEEP® publishes articles that use a wide variety of scientific approaches and address a broad range of topics. These may include, but are not limited to: Basic and neuroscience studies of sleep and circadian mechanisms In vitro and animal models of sleep, circadian rhythms, and human disorders Pre-clinical human investigations, including the measurement and manipulation of sleep and circadian rhythms Studies in clinical or population samples. These may address factors influencing sleep and circadian rhythms (e.g., development and aging, and social and environmental influences) and relationships between sleep, circadian rhythms, health, and disease Clinical trials, epidemiology studies, implementation, and dissemination research.
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