Chan Joey W Y, Li Chun-Tung, Chau Steven Wai Ho, Chan Ngan Yin, Li Tim Man-Ho, Huang Bei, Tsoh Joshua, Li Shirley X, Chong Kelvin K L, Roecklein Kathryn A, Wing Yun Kwok
Li Chiu Kong Family Sleep Assessment Unit, Department of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
Department of Psychiatry, Prince of Wales Hospital, Hong Kong SAR, China.
Sleep. 2025 Feb 10;48(2). doi: 10.1093/sleep/zsae239.
This study aimed to explore the relationship between post-illumination pupillary response (PIPR) with sleep and circadian measures in a community sample of healthy older adults.
Eligible participants were invited to complete a 1 week sleep diary and actigraphy, and provide an overnight urine sample to measure urinary 6-sulfatoxymelatonin (aMT6s). PIPR was defined as the (1) pupil constriction at 6 second poststimulus (PIPR-6s) and (2) for -30s beginning 10 seconds after stimulus (PIPR-30s), normalized as a percentage to the baseline pupil diameter, after 1 second of blue and 1 second of red light stimulus, respectively. The Net-PIPRs were reported by subtracting the PIPR to red stimulus from the PIPR to blue stimulus. The relationship between PIPR metrics to aMT6s and actigraphic rest-activity rhythm parameters was examined by generalized linear models.
A total of 48 participants were recruited (mean age: 62.6 ± 7.1 years, male: 44%). Both Net PIPR-6s and Net PIPR-30s were significantly associated with actigraphic rest-activity amplitude (B = 0.03, p = .001 and B = 0.03, p = .01, respectively) and actigraphic rest-activity mesor (B = 0.02, p = .001 and B = 0.03, p = .004, respectively). Additionally, the Net PIPR-30s were positively associated with overnight aMT6s level (B = 0.04, p = .03) and negatively associated with actigraphic rest-activity acrophase (B = -0.01, p = .004) in the fully adjusted models.
Attenuated PIPR is associated with a reduced actigraphic amplitude and mesor. The reduced retinal light responsivity may be a potential pathway contributing to impaired photic input to the circadian clock and resulted in age-related circadian changes in older adults.
本研究旨在探讨健康老年人社区样本中光照后瞳孔反应(PIPR)与睡眠及昼夜节律指标之间的关系。
符合条件的参与者被邀请完成为期1周的睡眠日记和活动记录仪监测,并提供一份夜间尿液样本以测量尿6 - 硫酸氧褪黑素(aMT6s)。PIPR被定义为:(1)刺激后6秒时的瞳孔收缩(PIPR - 6s),以及(2)刺激后10秒开始的-30秒内的瞳孔收缩(PIPR - 30s),分别在1秒蓝光和1秒红光刺激后,以相对于基线瞳孔直径的百分比进行标准化。净PIPR通过从蓝光刺激的PIPR中减去红光刺激的PIPR来报告。通过广义线性模型研究PIPR指标与aMT6s及活动记录仪静息 - 活动节律参数之间的关系。
共招募了48名参与者(平均年龄:62.6±7.1岁,男性:44%)。净PIPR - 6s和净PIPR - 30s均与活动记录仪静息 - 活动幅度显著相关(分别为B = 0.03,p = 0.001和B = 0.03,p = 0.01)以及活动记录仪静息 - 活动中值(分别为B = 0.02,p = 0.001和B = 0.03,p = 0.004)。此外,在完全调整模型中,净PIPR - 30s与夜间aMT6s水平呈正相关(B = 0.04,p = 0.03),与活动记录仪静息 - 活动峰相位呈负相关(B = -0.01,p = 0.004)。
PIPR减弱与活动记录仪记录的幅度和中值降低有关。视网膜光反应性降低可能是导致昼夜节律时钟的光输入受损并导致老年人出现与年龄相关的昼夜节律变化的潜在途径。