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Updated: Jan 21, 2026

Measuring Diurnal Rhythms in Autophagic and Proteasomal Flux
Published on: September 17, 2019
Twenty-four hour ocular and systemic diurnal rhythms in children
Lisa A Ostrin1, Ashutosh Jnawali1, Andrew Carkeet2
1College of Optometry, University of Houston, Houston, USA.
Insights
Ocular and systemic diurnal rhythms are robust in children, mirroring adult patterns. Axial length and intraocular pressure (IOP) variations may influence myopia development in pediatric populations.
Area of Science:
- Ophthalmology
- Chronobiology
- Pediatric Health
Background:
- Ocular diurnal rhythms are linked to various eye conditions like myopia and glaucoma.
- While well-documented in adults, diurnal rhythms in children remain under-examined.
Purpose of the Study:
- To investigate ocular and systemic diurnal rhythms over a 24-hour period in children.
- To compare pediatric diurnal rhythms with existing adult data.
Main Methods:
- 18 children (ages 5-14) wore activity monitors and underwent hourly measurements (blood pressure, heart rate, temperature, IOP, ocular biometry, OCT imaging).
- Saliva samples were collected for melatonin and cortisol analysis.
- Fourier analysis was used to determine diurnal variation amplitude and acrophase for each parameter.
Main Results:
- Significant 24-hour variations (p ≤ 0.005) were observed in most parameters, except anterior chamber depth.
- Axial length varied by 45.25 μm, IOP by 4.19 mmHg, and choroidal thickness by 26.25 μm, with distinct acrophases.
- Retinal layers (total, RPE+outer, inner segments) also showed significant diurnal changes.
Conclusions:
- Pediatric ocular and systemic diurnal rhythms are robust and comparable to adult patterns.
- Axial length and IOP were largely in phase, while choroidal thickness was in antiphase.
- These findings suggest potential implications for understanding myopia development in children.
Purpose:
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.
Methods:
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.
Results:
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.
Conclusions:
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.
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