Screen time, sleep, brain structural neurobiology, and sequential associations with child and adolescent psychopathology: Insights from the ABCD study

Author:

Zhao Yihong1ORCID,Paulus Martin P.23ORCID,Tapert Susan F.3ORCID,Bagot Kara S.4ORCID,Constable R. Todd5ORCID,Yaggi H. Klar67ORCID,Redeker Nancy S.8ORCID,Potenza Marc N.9101112ORCID

Affiliation:

1. Columbia University School of Nursing, New York, NY, USA

2. Laureate Institute for Brain Research, Tulsa, OK, USA

3. Department of Psychiatry, University of California, San Diego, CA, USA

4. Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles, CA, USA

5. Biomedical Engineering, Radiology and Biomedical Imaging, Interdepartmental Neuroscience Program, Yale University School of Medicine, New Haven, CT, USA

6. Department of Medicine, Yale School of Medicine, New Haven, CT, USA

7. VA Clinical Epidemiology Research Center, VA Connecticut HCS, West Haven, CT, USA

8. University of Connecticut School of Nursing, Storrs, CT, USA

9. Department of Psychiatry, Child Study Center, Department of Neuroscience, Yale University School of Medicine, New Haven, CT, USA

10. Connecticut Mental Health Center, New Haven, CT, USA

11. Connecticut Council on Problem Gambling, Wethersfield, CT, USA

12. Wu Tsai Institute, Yale University, New Haven, CT, USA

Abstract

AbstractBackground and AimsThe precise roles of screen media activity (SMA) and sleep problems in relation to child/adolescent psychopathology remain ambiguous. We investigated temporal relationships among sleep problems, SMA, and psychopathology and potential involvement of thalamus-prefrontal-cortex (PFC)-brainstem structural covariation.MethodsThis study utilized data from the Adolescent Brain Cognitive Development study (n = 4,641 ages 9–12) at baseline, Year1, and Year2 follow-up. Cross-Lagged Panel Models (CLPMs) investigated reciprocal predictive relationships between sleep duration/problems, SMA, and psychopathology symptoms. A potential mediating role of baseline Thalamus-PFC-brainstem covariation on SMA-externalizing relationships was examined.ResultsParticipants were divided into discovery (n = 2,359, 1,054 girls) and replication (n = 2,282, 997 girls) sets. CLPMs showed 1) bidirectional associations between sleep duration and SMA in late childhood, with higher frequency SMA predicting shorter sleep duration (β = −0.10 [95%CI: −0.16, −0.03], p = 0.004) and vice versa (β = −0.11 [95%CI: −0.18, −0.05], p < 0.001); 2) externalizing symptoms at age 10–11 predicting sleep problems (β = 0.11 [95%CI: 0.04, 0.19], p = 0.002), SMA (β = 0.07 [95%CI: 0.01, 0.13], p = 0.014), and internalizing symptoms (β = 0.09 [95%CI: 0.05, 0.13], p < 0.001) at age 11–12; and 3) externalizing behavior at age 10-11 partially mediating the relationship between baseline thalamus-PFC-brainstem covariation and SMA at age 11–12 (indirect effect = 0.032 [95%CI: 0.003, 0.067], p-value = 0.030). Findings were replicable.ConclusionWe found bi-directional SMA-sleep-duration associations in late childhood. Externalizing symptoms preceded future SMA and sleep disturbances and partially mediated relationships between structural brain covariation and SMA. The findings emphasize the need for understanding individual differences and developing and implementing integrated strategies addressing both sleep concerns and screen time to mitigate potential impacts on psychopathology.

Funder

Children and Screens

NIH

National Institutes of Health

Publisher

Akademiai Kiado Zrt.

Reference60 articles.

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