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.
It is demonstrated that endurance exercise performance is enhanced in the evening compared with the morning and suggested that behavioural markers of circadian phenotype are associated with the magnitude of diurnal variation in performance.
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
Skin temperature showed promising feasibility for in-field circadian rhythm estimation after only three days, potentially facilitating research on circadian rhythms and health and 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