College of Education, Psychology, and Social Work, Flinders University, Adelaide, South Australia, Australia.
Menzies Institute for Medical Research, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Acta Paediatr. 2023 May;112(5):1001-1010. doi: 10.1111/apa.16719. Epub 2023 Mar 3.
Investigate if childhood measures of sleep health are associated with epigenetic age acceleration in late adolescence.
Parent-reported sleep trajectories from age 5 to 17, self-reported sleep problems at age 17, and six measures of epigenetic age acceleration at age 17 were studied in 1192 young Australians from the Raine Study Gen2.
There was no evidence for a relationship between the parent-reported sleep trajectories and epigenetic age acceleration (p ≥ 0.17). There was a positive cross-sectional relationship between self-reported sleep problem score and intrinsic epigenetic age acceleration at age 17 (b = 0.14, p = 0.04), which was attenuated after controlling for depressive symptom score at the same age (b = 0.08, p = 0.34). Follow-up analyses suggested this finding may represent greater overtiredness and intrinsic epigenetic age acceleration in adolescents with higher depressive symptoms.
There was no evidence for a relationship between self- or parent-reported sleep health and epigenetic age acceleration in late adolescence after adjusting for depressive symptoms. Mental health should be considered as a potential confounding variable in future research on sleep and epigenetic age acceleration, particularly if subjective measures of sleep are used.
探究儿童时期的睡眠健康指标是否与青少年晚期的表观遗传年龄加速有关。
在来自雷因研究二代的 1192 名澳大利亚年轻人中,研究了从 5 岁到 17 岁的父母报告的睡眠轨迹、17 岁时的自我报告睡眠问题以及 17 岁时的 6 项表观遗传年龄加速测量值。
父母报告的睡眠轨迹与表观遗传年龄加速之间没有关系(p≥0.17)。17 岁时自我报告的睡眠问题评分与内在表观遗传年龄加速呈正相关(b=0.14,p=0.04),但在控制相同年龄的抑郁症状评分后,这种相关性减弱(b=0.08,p=0.34)。后续分析表明,这一发现可能代表了抑郁症状较高的青少年中更明显的过度疲劳和内在表观遗传年龄加速。
在调整抑郁症状后,自我或父母报告的睡眠健康与青少年晚期的表观遗传年龄加速之间没有关系。在未来关于睡眠和表观遗传年龄加速的研究中,应考虑心理健康作为潜在的混杂变量,特别是如果使用主观的睡眠测量值。