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韩国成年人睡眠质量与代谢综合征加速表观遗传衰老之间的关联。

The association between sleep quality and accelerated epigenetic aging with metabolic syndrome in Korean adults.

作者信息

Lee Ho-Sun, Kim Boram, Park Taesung

机构信息

Forensic Toxicology Division, Daegu Institute, National Forensic Service, Andong-si, Gyeongsangbuk-do, 39872, Korea.

Interdisciplinary Program in Bioinformatics, Seoul National University, Seoul, 08826, Korea.

出版信息

Clin Epigenetics. 2024 Jul 16;16(1):92. doi: 10.1186/s13148-024-01706-x.

Abstract

BACKGROUND

Healthy sleep is vital for maintaining optimal mental and physical health. Accumulating evidence suggests that sleep loss and disturbances play a significant role in the biological aging process, early onset of disease, and reduced lifespan. While numerous studies have explored the association between biological aging and its drivers, only a few studies have examined its relationship with sleep quality. In this study, we investigated the associations between sleep quality and epigenetic age acceleration using whole blood samples from a cohort of 692 Korean adults. Sleep quality of each participant was assessed using the validated Pittsburgh Sleep Quality Index (PSQI), which encompassed seven domains: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbance, use of sleep medication, and daytime dysfunction. Four epigenetic age accelerations (HorvathAgeAccel, HannumAgeAccel, PhenoAgeAccel, and GrimAgeAccel) and the pace of aging, DunedinPACE, were investigated for epigenetic aging estimates.

RESULTS

Among the 692 participants (good sleepers [n = 441, 63.7%]; poor sleepers [n = 251, 36.3%]), DunedinPACE was positively correlated with PSQI scores in poor sleepers ( =0.18, p < 0.01). GrimAgeAccel ( =0.18, p = 0.02) and DunedinPACE ( =0.01, p < 0.01) showed a statistically significant association with PSQI scores only in poor sleepers by multiple linear regression. In addition, every one-point increase in PSQI was associated with a 15% increase in the risk of metabolic syndrome (MetS) among poor sleepers (OR = 1.15, 95% CI = 1.03-1.29, p = 0.011). In MetS components, a positive correlation was observed between PSQI score and fasting glucose ( = 0.19, p < 0.01).

CONCLUSIONS

This study suggests that worsening sleep quality, especially in poor sleepers, is associated with accelerated epigenetic aging for GrimAgeAccel and DundinePACE with risk of metabolic syndrome. This finding could potentially serve as a promising strategy for preventing age-related diseases in the future.

摘要

背景

健康睡眠对于维持最佳身心健康至关重要。越来越多的证据表明,睡眠不足和睡眠障碍在生物衰老过程、疾病早发以及寿命缩短中起着重要作用。虽然众多研究探讨了生物衰老与其驱动因素之间的关联,但仅有少数研究考察了其与睡眠质量的关系。在本研究中,我们使用来自692名韩国成年人队列的全血样本,调查了睡眠质量与表观遗传年龄加速之间的关联。使用经过验证的匹兹堡睡眠质量指数(PSQI)评估每位参与者的睡眠质量,该指数涵盖七个领域:主观睡眠质量、入睡潜伏期、睡眠时间、习惯性睡眠效率、睡眠障碍、睡眠药物使用情况以及日间功能障碍。研究了四种表观遗传年龄加速指标(霍瓦斯年龄加速、汉纳姆年龄加速、表型年龄加速和格里姆年龄加速)以及衰老速度指标邓迪因PACE,以进行表观遗传衰老评估。

结果

在692名参与者中(睡眠良好者[n = 441,63.7%];睡眠不佳者[n = 251,36.3%]),睡眠不佳者的邓迪因PACE与PSQI评分呈正相关(r = 0.18,p < 0.01)。通过多元线性回归分析,仅在睡眠不佳者中,格里姆年龄加速(r = 0.18,p = 0.02)和邓迪因PACE(r = 0.01,p < 0.01)与PSQI评分存在统计学显著关联。此外,在睡眠不佳者中,PSQI每增加1分,代谢综合征(MetS)风险增加15%(OR = 1.15,95%CI = 1.03 - 1.29,p = 0.011)。在代谢综合征各组分中,观察到PSQI评分与空腹血糖之间呈正相关(r = 0.19,p < 0.01)。

结论

本研究表明,睡眠质量恶化,尤其是在睡眠不佳者中,与格里姆年龄加速和邓迪因PACE的表观遗传衰老加速以及代谢综合征风险相关。这一发现可能为未来预防与年龄相关疾病提供一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d017/11253334/86ce1380a1fe/13148_2024_1706_Fig1_HTML.jpg

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