Jun 2026· Chronobiology International· pp.
1-14
· 0 citations· 46 references
Medicine
TL;DR
The smaller circadian amplitude of WTA and PAA, the lesser sleep quality, and the smaller normalized amplitude of blue light exposure, independently of photoperiod, are associated with elevated leptin in Arctic residents.
Abstract
This hypothesis-driven study tested whether circadian amplitudes of wrist temperature (WTA), physical activity (PAA), and light exposure measured by actigraphy predicted morning leptin in 64 Arctic residents, and whether the CLOCK 3111 polymorphism (rs1801260) modulated these predictions. Actigraphy measures (circadian amplitudes of WT, PA, and light exposure) and morning leptin concentrations were assessed across seasons with contrasting photoperiods. Multivariate regression models identified leptin predictors. Post-hoc analyses examined WTA-leptin relationships, considering CLOCK 3111 genotype and an exploratory leptin threshold of 13 ng/mL. A multivariate analysis adjusted for the photoperiod revealed significant negative associations between leptin and WTA (β = -0.344), PAA (β = -0.323) and sleep efficiency (β = -0.265) that were retained after further adjustment for age, sex and indigeneity. In the fully adjusted model, a larger normalized amplitude of blue light exposure (NA BLE) was associated with increased WTA (β = 0.256) and lower leptin (β = -0.171). The CLOCK 3111 polymorphism modulated the WTA - leptin relationship, with a strong negative correlation in TT individuals (r = -0.509) and a non-significant trend towards a positive association in CC individuals (r = 0.282), Δr = 0.791, z = 2.31, p = 0.021. In CLOCK 3111 TT individuals, those with a WTA <1°C had significantly higher odds (OR = 3.93, 95% CI: 1.69-9.17, p = 0.0015) and increased relative risk (RR = 2.70, 95% CI: 1.47-4.99, p = 0.0014) of having a morning leptin ≥13 ng/mL, compared to those with a WTA >1.5°C. Overall, the smaller circadian amplitude of WTA and PAA, the lesser sleep quality, and the smaller normalized amplitude of blue light exposure (NA BLE), independently of photoperiod, are associated with elevated leptin in Arctic residents. The CLOCK 3111 polymorphism modulates the WTA-leptin relationship. For CLOCK 3111 TT individuals, a small WTA (<1°C) may identify those at risk of elevated morning leptin (≥13 ng/mL), informing metabolic risk assessment in unique environments.
PURPOSE
Time-of-day variation in exercise performance is well established, but the contribution of circadian phenotype to the magnitude of these differences remains unclear. This study examined diurnal variation in aerobic exercise performance and determined whether chronotype and sleep timing were associated with morning-evening differences in performance.
METHODS
Twenty-four healthy young adults (12 male, 12 female) completed a randomised crossover protocol consisting of a 10-min cycling time trial performed in the morning (08:00-09:00) and evening (17:00-18:00). Pre-trial sleep, diet, and physical activity were standardised, and circadian phenotype was characterised using the Composite Morningness Questionnaire and 7-day actigraphy.
RESULTS
Mean power, peak power, and distance covered were all significantly higher in the evening compared with morning (p < 0.01). Chronotype (r = - 0.47, p = 0.019) and sleep midpoint (r = 0.52, p = 0.003) were significantly associated with the magnitude of the diurnal performance difference, accounting for 22% and 27% of the variance, respectively. Heart rate, blood lactate, and perceived exertion responses were similar between conditions, indicating comparable physiological strain. Core temperature was higher in the evening (p = 0.026), but did not explain performance differences.
CONCLUSIONS
These findings demonstrate that endurance exercise performance is enhanced in the evening compared with the morning and suggest that behavioural markers of circadian phenotype are associated with the magnitude of diurnal variation in performance. Time-of-day and circadian phenotype should therefore be considered when optimising exercise testing and prescription.
A. Singh, Sanjida Ahmed, S. Hesketh· European Journal of Applied...· 0 citations
The findings suggest that I394T‐C carriers exhibit features of the circadian phenotype commonly observed in older cohorts, including reduced rhythm robustness and lower melatonin levels, and support a role for this variant in interindividual differences in light sensitivity and circadian function.
Jesús Vicente-Martínez, M. Bonmati-Carrion, Ana María López-Parra et al.· Journal of Pineal Research· 0 citations
Estimating circadian rhythms often relies on intrusive and costly methods like melatonin sampling, misfitting in longitudinal field studies. Alternatively, ambulatory activity monitoring is frequently used, yet requires week-long data and signals fitting poorly with cosinor models. Ambulatory skin temperature monitoring is promising, but its feasibility, reliability, and robustness to homeostatic sleep pressure remain understudied. We collected sensor data in a randomized crossover field study manipulating sleep duration (8 h vs. 4 h time-in-bed, three consecutive nights) among 17 healthy participants (19-32 years old). Activity and skin temperatures (distal, proximal, distal-proximal gradient) were continuously monitored across conditions. Cosinor analysis estimated rhythm parameters (amplitude, mesor, acrophase) and goodness of fit. Non-parametric tests and linear mixed-effect models assessed difference and stability across sleep conditions. Cosinor models fitted better on skin temperature than activity-based data. Sleep restriction affected activity rhythms (reduced amplitude, delayed acrophase, increased mesor). Beside a reduced distal temperature amplitude in sleep restriction, skin temperature rhythm showed no statistically significant moderations by sleep. Rhythm parameters between data types did not significantly correlate. Skin temperature showed promising feasibility for in-field circadian rhythm estimation after only three days, potentially facilitating research on circadian rhythms and health. Validation against core body temperature and melatonin sampling is warranted.
Vaida T R Verhoef, K.C.H.J. Smolders, Geert Peeters et al.· Chronobiology International· 0 citations
Objective Exercise timing may influence metabolic responses and body composition, but the extent to which circadian genetic variation contributes remains unclear. The PER3 rs228697 polymorphism has been linked to chronotype-related traits, although its relevance to exercise timing remains uncertain. This exploratory study examined whether body-composition responses to morning versus afternoon moderate-intensity continuous training (MICT) differed according to PER3 rs228697 genotype in overweight/obese university students. Methods In this 8-week supervised intervention, 31 overweight/obese university students performed MICT in the morning (7:00–10:00) or afternoon (16:00–19:00). Participants with the CC genotype were allocated to a morning training group (CC-AM) or an afternoon training group (CC-PM), and G-allele carriers were included in an afternoon group (G-PM). Body weight, body mass index (BMI), waist circumference, body fat percentage, total fat mass, and regional fat mass were assessed before and after the intervention. Circadian preference, physical activity, sleep quality, and fatigue were also evaluated. Because the G-PM subgroup was very small, findings for this subgroup were treated as exploratory. Results Across the overall sample, body weight, BMI, waist circumference, body fat percentage, and total fat mass decreased over the 8-week intervention. In descriptive subgroup analyses, the CC-PM group showed larger reductions in several body-composition outcomes, including body weight, BMI, waist circumference, body fat percentage, and total fat mass, than the CC-AM group. A similar pattern was observed for several regional fat measures, particularly trunk, android, and gynoid fat mass. By contrast, findings for G-allele carriers were difficult to interpret because of the very small subgroup size. Estimated between-group differences were generally modest and imprecise, and behavioral chronotype did not clearly correspond with PER3 genotype. Conclusions In this exploratory sample of overweight/obese university students, 8 weeks of MICT was associated with favorable changes in several body-composition outcomes. Among CC genotype carriers, afternoon training was associated with descriptively greater improvements than morning training; however, the estimates were imprecise and do not support strong conclusions regarding genotype-based exercise-time matching based on PER3 rs228697 alone. Larger, well-controlled studies with objective circadian phenotyping are needed to clarify the potential role of genotype-informed exercise timing in personalized weight management.
Yuchen Wang, Chunyan Xu, Juan Tong· Frontiers in Physiology· 0 citations