College of Optometry, University of Houston, Houston, USA.
School of Optometry and Vision Science, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Australia.
Ophthalmic Physiol Opt. 2019 Sep;39(5):358-369. doi: 10.1111/opo.12633. Epub 2019 Jul 22.
Ocular diurnal rhythms have been implicated in myopia, glaucoma, diabetes, and other ocular pathologies. Ocular rhythms have been well described in adults; however, they have not yet been fully examined in children. The goal of this study was to investigate ocular and systemic diurnal rhythms over 24 h in children.
Subjects, ages 5 to 14 years (n = 18), wore a light, sleep, and activity monitor for one week to assess habitual sleep/wake patterns, then underwent diurnal measurements every 4 h for 24 h. Measurements included blood pressure, heart rate, body temperature, intraocular pressure (IOP), ocular biometry, and optical coherence tomography imaging. Saliva was collected for melatonin and cortisol analysis. Mean ocular perfusion pressure was calculated from IOP and blood pressure. Central corneal thickness, corneal power, anterior chamber depth, lens thickness, vitreous chamber depth, and axial length were determined from biometry. Total retinal thickness, retinal pigment epithelium (RPE) + photoreceptor outer segment thickness, photoreceptor inner segment thickness, and choroidal thickness were determined for a 1 mm diameter centred on the fovea. Subjects' amplitude and acrophase of diurnal variation for each parameter were determined using Fourier analysis, and mean acrophase was calculated using unit vector averaging.
Repeated measures analysis of variance (ANOVA) showed that all parameters except anterior chamber depth exhibited significant variations over 24 h (p ≤ 0.005 for all). Axial length underwent diurnal variation of 45.25 ± 6.30 μm with an acrophase at 12.92 h, and choroidal thickness underwent diurnal variation of 26.25 ± 2.67 μm with an acrophase at 1.90 h. IOP was approximately in phase with axial length, with a diurnal variation of 4.19 ± 0.50 mmHg and acrophase at 11.37 h. Total retinal thickness underwent a significant diurnal variation of 4.09 ± 0.39 μm with an acrophase at 15.04 h. The RPE + outer segment layer was thickest at 3.25 h, while the inner segment layer was thickest at 14.95 h. Melatonin peaked during the dark period at 2.36 h, and cortisol peaked after light onset at 9.22 h.
Ocular and systemic diurnal rhythms were robust in children and similar to those previously reported in adult populations. Axial length and IOP were approximately in phase with each other, and in antiphase to choroidal thickness. These findings may have important implications in myopia development in children.
昼夜节律已被认为与近视、青光眼、糖尿病和其他眼部疾病有关。昼夜节律在成年人中已经得到了很好的描述;然而,它们在儿童中尚未得到充分研究。本研究的目的是调查儿童 24 小时内的眼部和全身昼夜节律。
研究对象为 5 至 14 岁(n=18)的儿童,他们佩戴轻便的睡眠和活动监测器一周,以评估习惯性的睡眠/觉醒模式,然后每 4 小时进行一次 24 小时的昼夜测量。测量包括血压、心率、体温、眼内压(IOP)、眼部生物测量和光学相干断层扫描成像。收集唾液进行褪黑素和皮质醇分析。平均眼灌注压由 IOP 和血压计算得出。中央角膜厚度、角膜屈光力、前房深度、晶状体厚度、玻璃体腔深度和眼轴从生物测量中确定。以黄斑为中心,直径为 1 毫米的区域内确定视网膜总厚度、视网膜色素上皮(RPE)+光感受器外节厚度、光感受器内节厚度和脉络膜厚度。使用傅立叶分析确定每个参数的昼夜变化幅度和峰值时间,并使用单位向量平均计算平均峰值时间。
重复测量方差分析(ANOVA)显示,除前房深度外,所有参数均显示出 24 小时内的显著变化(所有 p 值均≤0.005)。眼轴的昼夜变化为 45.25±6.30μm,峰值时间为 12.92 小时,脉络膜厚度的昼夜变化为 26.25±2.67μm,峰值时间为 1.90 小时。IOP 与眼轴几乎同步,昼夜变化为 4.19±0.50mmHg,峰值时间为 11.37 小时。视网膜总厚度的昼夜变化显著,为 4.09±0.39μm,峰值时间为 15.04 小时。RPE+外节层最厚的时间为 3.25 小时,而内节层最厚的时间为 14.95 小时。褪黑素在夜间达到峰值,时间为 2.36 小时,皮质醇在光照开始后达到峰值,时间为 9.22 小时。
儿童的眼部和全身昼夜节律非常明显,与成人中的昼夜节律相似。眼轴和 IOP 彼此几乎同步,与脉络膜厚度相反。这些发现可能对儿童近视的发展有重要意义。