Insomnia trajectories predict chronic inflammation over 2 years at the transition to adulthood

Author:

Zhai Shuang1,Li Tingting1,Zhang Dan1,Qu Yang1,Xie Yang1,Wu Xiaoyan123ORCID,Zou Liwei23,Tao Fangbiao123,Tao Shuman234ORCID

Affiliation:

1. Department of Maternal, Child and Adolescent Health, School of Public Health Anhui Medical University Hefei Anhui People's Republic of China

2. MOE Key Laboratory of Population Health Across Life Cycle Hefei Anhui People's Republic of China

3. Anhui Provincial Key Laboratory of Population Health and Aristogenics Anhui Medical University Hefei Anhui People's Republic of China

4. Department of Ophthalmology The Second Hospital of Anhui Medical University Hefei Anhui People's Republic of China

Abstract

SummaryInsomnia in adolescents is an important public health concern, as its impacts on both their current and future physical and mental health has been discussed. However, few longitudinal studies have examined insomnia and chronic inflammation at the transition from adolescence to adulthood. This study aimed to examine the predictive effects of insomnia and insomnia trajectories on inflammation in college students by using a prospective design. Using data from the College Student Behaviour and Health Cohort Study, which was conducted between April 2019 and April 2021, with an interval of 6 months. We investigated the associations between insomnia trajectories from Year 1 to Year 3 and five inflammatory biomarkers (C‐reactive protein [CRP], tumour necrosis factor [TNF]‐α, interleukin [IL]‐6, IL‐1β, IL‐10) at Year 3. The association of insomnia symptoms at baseline, Wave 1 or Wave 2 with inflammatory biomarkers at Wave 4 were also assessed. A total of 312 college students (males: 51.6%) aged 16–26 years (mean [SD] 18.82 [1.22] years) were analysed. We identified two insomnia trajectory classes: increasing insomnia (n = 63 [20.2%]) and decreasing insomnia (n = 249 [79.8%]). Generalised linear model analysis revealed that insomnia symptoms at Wave 1 were associated with significantly elevated CRP and TNF‐α levels at Wave 4. Increasing insomnia trajectories predicted consistently higher levels of CRP, TNF‐α and IL‐10. However, after adjusting for potential confounders, these associations were significantly attenuated. Overall, the findings suggest that insomnia symptoms affect chronic inflammation at the transition to adulthood. Our study needs to be replicated in larger cohorts to further explore how inflammation interacts with insomnia to increase the susceptibility to adverse health conditions.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Behavioral Neuroscience,Cognitive Neuroscience,General Medicine

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