Department of Psychobiology, Universidade Federal de São Paulo, São Paulo, Brazil.
Center for Investigation and Research in Sleep, Department of Internal Medicine, Lausanne University Hospital, Lausanne, Switzerland.
J Clin Sleep Med. 2018 Dec 15;14(12):2037-2045. doi: 10.5664/jcsm.7532.
We aimed to determine the association between short telomere length, sleep parameters, and sleep disorders in an adult general population sample.
As part of the EPISONO cohort (São Paulo, Brazil), 925 individuals answered questionnaires, underwent a full-night polysomnography and clinical assessment, and had peripheral blood collected for DNA extraction. Insomnia was diagnosed based on the Diagnostic and Statistical Manual of Mental Disorders, 4th edition; and obstructive sleep apnea was defined according to apnea-hypopnea index. For the objective insomnia phenotype, we combined insomnia diagnosis with total sleep time from polysomnography with a cutoff of 360 minutes, allowing the classification of six groups. Self-reported sleep duration was used to classify the individuals as short (< 6 hours), average (6 to 8 hours) and long (> 8 hours) sleepers. The leukocyte telomere length was measured using quantitative real-time polymerase chain reaction. Based on its distribution, we considered leukocyte telomere length < 10th percentile as short telomere and leukocyte telomere length ≥ 10th percentile as non-short telomere.
After adjusting for sex, age, and body mass index, only insomnia disorder (odds ratio [OR] = 2.654, 95% confidence interval [CI] = 1.025-6.873, = .044), insomnia disorder total sleep time < 360 minutes (OR = 4.205, 95% CI = 1.097-16.117, = .036) and long sleepers (OR = 2.177, 95% CI = 1.189- 3.987, = .012) were associated with short telomere.
Our findings support the existence of an association among insomnia, insomnia phenotype, and self-reported long sleep duration with the maintenance of telomere length.
A commentary on this article appears in this issue on page 1975.
我们旨在确定短端粒长度、睡眠参数和睡眠障碍在成人普通人群样本中的相关性。
作为 EPISONO 队列(巴西圣保罗)的一部分,925 名个体回答了调查问卷,进行了整夜多导睡眠图和临床评估,并采集了外周血进行 DNA 提取。失眠根据《精神障碍诊断与统计手册》第 4 版进行诊断;阻塞性睡眠呼吸暂停根据呼吸暂停低通气指数定义。对于客观失眠表型,我们将失眠诊断与多导睡眠图中的总睡眠时间(临界值为 360 分钟)相结合,将个体分为六组。自我报告的睡眠时间用于将个体分为短(<6 小时)、平均(6-8 小时)和长(>8 小时)睡眠时间者。使用实时定量聚合酶链反应测量白细胞端粒长度。根据其分布,我们将白细胞端粒长度<第 10 百分位数定义为短端粒,白细胞端粒长度≥第 10 百分位数定义为非短端粒。
在校正性别、年龄和体重指数后,仅失眠障碍(比值比[OR] = 2.654,95%置信区间[CI] = 1.025-6.873,P =.044)、失眠障碍总睡眠时间<360 分钟(OR = 4.205,95% CI = 1.097-16.117,P =.036)和长睡眠者(OR = 2.177,95% CI = 1.189-3.987,P =.012)与短端粒有关。
我们的研究结果支持失眠、失眠表型和自我报告的长睡眠时间与端粒长度维持之间存在关联。
本文的一篇评论见本期第 1975 页。