医学
多导睡眠图
内科学
超重
内分泌学
体质指数
睡眠(系统调用)
胰岛素
葡萄糖稳态
糖耐量试验
睡眠架构
早晨
阻塞性睡眠呼吸暂停
睡眠阶段
慢波睡眠
碳水化合物代谢
胰岛素抵抗
呼吸暂停
脑电图
精神科
计算机科学
操作系统
作者
Yin Zhu,Albert Martin Li,Chun Ting Au,Alice Pik Shan Kong,Jihui Zhang,Chun Kwok Wong,Juliana C.N. Chan,Yun Kwok Wing
标识
DOI:10.1111/1753-0407.12138
摘要
Short sleep duration is a contributing factor for decreased insulin sensitivity and hyperglycemia. Sleep architecture represents a cyclical pattern of sleep that shifts between sleep Stages N1, N2, N3 (slow wave sleep) and Stage R (rapid eye movement sleep). The aim of the present study was to examine the association between sleep architecture and glucose and insulin metabolism in both normal weight and overweight/obese children and adolescents.A total of 118 subjects participated in the study. Subjects under-went overnight polysomnography (PSG) when the percentage of total sleep time (% TST) spent at each sleep stage was recorded and an oral glucose tolerance test together was performed the next morning. We assessed glucose tolerance, insulin sensitivity and pancreatic β-cell function using 2-h glucose levels, the Matsuda index (IS(OGTT)), and insulin secretion-sensitivity index-2 (ISSI-2), respectively.After adjustment for age, gender, body mass index z-score, pubertal status, and obstructive apnea hypopnea index, Stage N3 (% TST) was positively associated with IS(OGTT), whereas Stage N1 (%TST) exerted an opposite effect on IS(OGTT). Higher sleep efficiency and longer TST were independently associated with lower 2-h glucose levels, higher ISSI-2 and/or higher IS(OGTT).Stage N3, sleep efficiency and TST were protective factors in maintaining glucose and insulin homeostasis; however, Stage N1 functioned in the opposite direction.
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