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将健康行为作为连接青春期较早开始与青少年晚期表观遗传加速衰老的机制进行研究。

Examining Health Behaviors as Mechanisms Linking Earlier Pubertal Timing with Accelerated Epigenetic Aging in Late Adolescence.

作者信息

Goering Marlon, Tiwari Hemant K, Patki Amit, Espinoza Carlos N, Knight David C, Mrug Sylvie

机构信息

Department of Psychology, University of Alabama at Birmingham, 1720 2nd Ave South, Birmingham, AL, USA.

Department of Biostatistics, University of Alabama at Birmingham, 1720 2nd Ave South, Birmingham, AL, USA.

出版信息

J Youth Adolesc. 2025 Mar;54(3):750-768. doi: 10.1007/s10964-024-02096-2. Epub 2024 Oct 3.

Abstract

Earlier pubertal timing is associated with accelerated epigenetic aging, but the underlying mechanisms are not well understood. This three-wave longitudinal study examined negative health behaviors, specifically substance use, short sleep duration, and poor diet quality in middle adolescence, as mediators of links between earlier phenotypic and perceived pubertal timing measured in early adolescence and epigenetic aging on three epigenetic clocks in late adolescence (GrimAge, DunedinPACE, and PhenoAge). Phenotypic pubertal timing measured physical pubertal maturation relative to chronological age, whereas perceived pubertal timing was based on adolescents' subjective interpretation of their pubertal timing relative to their peers. Participants included 1213 youth (51% female, 49% male; 62% Black, 34% White) who participated during early adolescence (mean age = 13.10 years), middle adolescence (mean age = 16.1 years) and late adolescence (mean age = 19.7 years). Results from a mediation model revealed a mediation effect of earlier phenotypic pubertal timing on accelerated GrimAge in late adolescence through higher substance use during middle adolescence. There was also a direct effect of earlier phenotypic pubertal timing on accelerated DunedinPACE in males. Sleep duration and diet quality did not emerge as mediators but shorter sleep duration predicted accelerated GrimAge in females. These findings suggest that higher substance use presents a mechanism through which earlier maturing youth experience faster epigenetic aging that puts them at risk for poorer health across the lifespan.

摘要

青春期提前与表观遗传衰老加速有关,但其潜在机制尚不清楚。这项三波纵向研究考察了负面健康行为,特别是青少年中期的物质使用、短睡眠时间和不良饮食质量,作为青少年早期测量的表型和感知青春期时间与青少年晚期三个表观遗传时钟(GrimAge、达尼丁PACE和PhenoAge)上的表观遗传衰老之间联系的中介因素。表型青春期时间测量的是相对于实际年龄的身体青春期成熟度,而感知青春期时间是基于青少年相对于同龄人对自己青春期时间的主观解读。参与者包括1213名青少年(51%为女性,49%为男性;62%为黑人,34%为白人),他们在青少年早期(平均年龄 = 13.10岁)、青少年中期(平均年龄 = 16.1岁)和青少年晚期(平均年龄 = 19.7岁)参与了研究。中介模型的结果显示,青少年中期较高的物质使用介导了青少年早期表型青春期时间提前与青少年晚期GrimAge加速之间的关系。青少年早期表型青春期时间提前对男性的达尼丁PACE加速也有直接影响。睡眠时间和饮食质量并未成为中介因素,但较短的睡眠时间预示着女性的GrimAge加速。这些发现表明,较高的物质使用是早熟青少年经历更快表观遗传衰老的一种机制,这使他们在整个生命周期中面临健康状况较差的风险。

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