在NIH AARP队列中,睡眠时间与口腔微生物群多样性和组成的改变有关。

Kathryn R Dalton, Vicky C Chang, Mikyeong Lee, Katherine Maki, Pedro Saint-Maurice, Vaishnavi Purandare, Xing Hua, Yunhu Wan, Casey L Dagnall, Kristine Jones, Belynda D Hicks, Amy Hutchinson, Linda M Liao, Mitchell H Gail, Jianxin Shi, Rashmi Sinha, Christian C Abnet, Stephanie J London, Emily Vogtmann
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引用次数: 0

摘要

研究目的:微生物群被认为是睡眠改变对健康不利影响的一个因素。口腔微生物群是一个多方面的微生物群落,影响许多健康功能。然而,关于睡眠和口腔微生物群之间关系的数据有限,而且没有研究将生活方式和环境暴露结合起来。方法:在NIH-AARP队列的一个子集(N= 1139)中,我们通过16S rRNA基因扩增子测序检查了自我报告的睡眠时间与口腔微生物组之间的关系。统计模型根据人口统计学特征进行了调整。其他模型研究了各种生活方式和社区暴露对睡眠-口腔微生物组关联的作用。结果:与报告推荐的平均睡眠时间为7-8小时的参与者(n=702)相比,报告睡眠时间短(6小时或更少,n=284)的参与者在样本内口腔微生物多样性持续下降[例如,观察到的扩增子序列变异数差异-8.681,p值=0.009]。在睡眠不足的一组中,更有可能缺少几种细菌属。我们发现,与推荐睡眠时间组相比,短睡眠组链球菌和罗氏菌的相对丰度较高,梭杆菌、特托菌和弯曲杆菌的相对丰度较低。在控制生活方式和社区因素后,结果是一致的。结论:我们的研究结果为短睡眠时间与口腔微生物多样性和组成之间的关联提供了证据。这表明口腔细菌可能在与睡眠健康相关的机制中发挥作用。提高对生理途径的理解可以帮助设计有益于改善整体睡眠健康的干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep duration associated with altered oral microbiome diversity and composition in the NIH AARP cohort.

Study objectives: The microbiome is proposed as a contributor to the adverse health impacts from altered sleep. The oral microbiome is a multifaceted microbial community that influences many health functions. However, data on the relationship between sleep and the oral microbiome are limited, and no studies have incorporated lifestyle and environmental exposures.

Methods: Within a subset (N=1,139) of the NIH-AARP cohort, we examined the association between self-reported sleep duration and the oral microbiome via 16S rRNA gene amplicon sequencing. Statistical models were adjusted for demographic characteristics. Additional models examined the role of various lifestyle and neighborhood exposures on the sleep-oral microbiome association.

Results: Compared to participants reporting the recommended 7-8 hours average sleep duration (n=702), those reporting short sleep (6 or fewer hours, n=284) had consistently decreased within-sample oral microbial diversity [e.g. number of observed amplicon sequence variants difference -8.681, p-value=0.009]. Several bacterial genera were more likely to be absent in the short sleep group. We found a higher relative abundance of Streptococcus and Rothia, and lower abundance of Fusobacterium, Atopobium, and Campylobacter in the short compared to the recommended sleep duration group. Results were consistent when controlling for lifestyle and neighborhood factors.

Conclusions: Our findings provide evidence for an association of short sleep duration with oral microbial diversity and composition. This suggests that oral bacteria may play a possible mechanistic role related to sleep health. Improved understanding of physiological pathways can aid in the design of interventions that may beneficially improve overall sleep health.

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