0201 Sleep duration and timing is prospectively linked with increases in insulin resistance over late adolescence. (25th May 2022)

• Record Type: Journal Article
• Authors: Jansen, Erica; Burgess, Helen; Chervin, Ronald; O'Brien, Louise; Dolinoy, Dana; Tellez-Rojo, Martha Maria; Cantoral, Alejandra; Olascoaga-Torres, Libni; Lee, Joyce; Dunietz, Galit; Peterson, Karen
• Is Part Of: Sleep. Volume 45(2022)Supplement 1
• Page Start: A92
• Page End: A92
• Publication Date: 2022-05-25
• Subjects: Sleep -- Physiological aspects -- Periodicals; Sleep disorders -- Periodicals; Sommeil -- Aspect physiologique -- Périodiques; Sommeil, Troubles du -- Périodiques; Sleep disorders; Sleep -- Physiological aspects; Sleep -- physiological aspects; Sleep Wake Disorders; Psychophysiology; Electronic journals; Periodicals; 616.8498
• DOI: 10.1093/sleep/zsac079.199
• Languages: English
• ISSNs: 0161-8105

Abstract

Abstract: Introduction: During puberty, adolescents experience a period of transient insulin resistance (IR) that normalizes upon full maturation. Yet, IR continues to rise for some adolescents, increasing metabolic disease and type 2 diabetes risk in adulthood. Whether short sleep duration and/or later sleep timing are risk factors for persistently increasing IR in late adolescence has not been explored. Methods: The study population includes 362 adolescents from Mexico City enrolled in a longitudinal birth cohort (ELEMENT study). Beginning in 2015, when participants were between the ages of 9 and 17, there were 2 clinic visits that occurred approximately 2 years apart. During the visit, a fasting blood sample and anthropometric measurements were taken. Insulin resistance was assessed with glucose and insulin via HOMA-IR. Four groups were defined using puberty-specific cutpoints for IR: normal HOMA-IR over the follow-up period (reference), transition from normal to IR, transition from IR to normal, and IR at both time points. Baseline sleep assessments (sleep duration, timing, and variability of both duration and timing) were measured with 7-day actigraphy. Multinomial logistic regression models were used to evaluate associations between sleep duration and timing with HOMA-IR categories, adjusting for age, sex, and baseline pubertal status Results: Seventeen percent of the sample developed insulin resistance over the follow-up period. Adolescents ≥1 hour below the sleep duration recommendations-for-age were over twice as likely to be in the group that developed IR compared to the normal group (95% CI 1.1, .9; P for trend=0.03). Similarly, adolescents who had a sleep midpoint later than 4:36 AM were 2.77 times as likely to be in the increasing HOMA-IR category (95% CI 1.0, 7.5; P for trend=0.05). Interestingly, there was no evidence that changes in adiposity over follow-up mediated associations between sleep and insulin resistance. Conclusion: Insufficient sleep duration and late sleep timing were independently associated with development of IR over a 2-year period in peri-puberty. Adequate sleep during the pubertal period may promote metabolic health into young adulthood, independent of any changes in adiposity. Support (If Any): Dr. Jansen is supported by K01HL151673. The study is supported by P01 ES02284401.