Sander Laura, Oommen Grace, Brophy Conor, Bohus-Roper Silver, Chiaro Giacomo, Bremner Fion, Iodice Valeria
Autonomic Unit, The National Hospital for Neurology and Neurosurgery, London, UK.
Department of Brain Repair and Rehabilitation, University College London Queen Square Institute of Neurology, London, UK.
Eur J Neurol. 2025 Aug;32(8):e70320. doi: 10.1111/ene.70320.
Pupillary function is frequently impaired in autonomic disorders, and biomarkers for early diagnosis and disease progression are urgently needed. Pupillometry allows for noninvasive ocular autonomic evaluation. This prospective study technically and clinically validates a handheld monocular pupillometer available for broad application as an autonomic screening tool in autonomic disorders.
A total of 40 controls and 100 patients with autonomic disorders underwent pupillometry using the PLR-4000(NeurOptics). Pupillary parasympathetic and sympathetic function were assessed by responses to a light stimulus and to 0.5% apraclonidine eye drops, respectively. Test-retest assessments and validations against a binocular device were performed.
In healthy controls, the mean light reflex ratio was 42% ± 5.7% and the median response to apraclonidine was -5.0% (-8.8%-2.8%). Monocular and binocular pupillometers presented similar results. Test-retest experiments showed: median light response difference 3.0% (1.0%-4.8%), median % difference in response to apraclonidine 5.2% (2.2%-10.6%). In patients with neurodegenerative disorders (n = 24), autonomic neuropathies (n = 39), and autonomic ganglionopathies (n = 9), pupillary abnormalities were very prevalent (52%, 45%, and 100%, respectively). All patients with intermittent autonomic disorders had normal pupillomotor function.
The presented device provides accurate, reproducible assessments of pupillary autonomic function in healthy controls and patients with autonomic disorders. With normative data provided, it is an easily accessible, well-tolerated tool to quantitatively assess pupillomotor innervation in a broad clinical setting. Further studies are warranted to explore its potential as a noninvasive biomarker, complementing standard autonomic function tests for early detection, monitoring disease progression, and evaluating treatment response in disorders with autonomic failure.
自主神经紊乱时瞳孔功能常受损,迫切需要用于早期诊断和疾病进展的生物标志物。瞳孔测量可进行无创性眼自主神经评估。本前瞻性研究在技术和临床层面验证了一种手持式单眼瞳孔测量仪,可广泛用作自主神经紊乱的自主神经筛查工具。
共40名对照者和100名自主神经紊乱患者使用PLR - 4000(NeurOptics)进行瞳孔测量。分别通过对光刺激和0.5%阿可乐定滴眼液的反应评估瞳孔副交感神经和交感神经功能。进行了重测评估以及与双目设备的验证。
在健康对照者中,平均光反射率为42%±5.7%,对阿可乐定的中位反应为 - 5.0%(-8.8% - 2.8%)。单眼和双目瞳孔测量仪结果相似。重测实验显示:光反应中位差异为3.0%(1.0% - 4.8%),对阿可乐定反应的中位百分比差异为5.2%(2.2% - 10.6%)。在神经退行性疾病患者(n = 24)、自主神经病变患者(n = 39)和自主神经节病变患者(n = 9)中,瞳孔异常非常普遍(分别为52%、45%和100%)。所有间歇性自主神经紊乱患者的瞳孔运动功能均正常。
所展示的设备能对健康对照者和自主神经紊乱患者的瞳孔自主神经功能进行准确、可重复的评估。有了提供的规范数据,它是一种易于获取、耐受性良好的工具,可在广泛的临床环境中定量评估瞳孔运动神经支配。有必要进一步研究探索其作为无创生物标志物的潜力,以补充标准自主神经功能测试,用于早期检测、监测疾病进展以及评估自主神经功能衰竭疾病的治疗反应。