Sleep disturbances in ADHD: investigating the contribution of polygenic liability for ADHD and sleep-related phenotypes

被引:0
作者
Katie J. S. Lewis
Joanna Martin
Alice M. Gregory
Richard Anney
Anita Thapar
Kate Langley
机构
[1] Cardiff University,MRC Centre for Neuropsychiatric Genetics and Genomics
[2] Goldsmiths,Department of Psychology
[3] University of London,School of Psychology
[4] Cardiff University,undefined
来源
European Child & Adolescent Psychiatry | 2023年 / 32卷
关键词
Sleep; ADHD; Comorbidity; Polygenic scores;
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学科分类号
摘要
Sleep disturbances are common in attention deficit hyperactivity disorder (ADHD) and associated with poor outcomes. We tested whether, in children with ADHD, (1) polygenic liability for sleep phenotypes is over- or under-transmitted from parents, (2) this liability is linked to comorbid sleep disturbances, and (3) ADHD genetic risk is associated with comorbid sleep disturbances. We derived polygenic scores (PGS) for insomnia, chronotype, sleep duration, and ADHD, in 758 children (5–18 years old) diagnosed with ADHD and their parents. We conducted polygenic transmission disequilibrium tests for each sleep PGS in complete parent–offspring ADHD trios (N = 328) and an independent replication sample of ADHD trios (N = 844). Next, we tested whether insomnia, sleep duration, and ADHD PGS were associated with co-occurring sleep phenotypes (hypersomnia, insomnia, restless sleep, poor sleep quality, and nightmares) in children with ADHD. Children’s insomnia and chronotype PGS did not differ from mid-parent average PGS but long sleep duration PGS were significantly over-transmitted to children with ADHD. This was supported by a combined analysis using the replication sample. Insomnia, sleep duration, and ADHD PGS were not associated with comorbid sleep disturbances. There is weak evidence that children with ADHD over-inherit polygenic liability for longer sleep duration and do not differentially inherit polygenic liability for insomnia or chronotype. There was insufficient evidence that childhood sleep disturbances were driven by polygenic liability for ADHD or sleep traits, suggesting that sleep disturbances in ADHD may be aetiologically different to general population sleep phenotypes and do not index greater ADHD genetic risk burden.
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页码:1253 / 1261
页数:8
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  • [1] Yoon SYR(2012)Sleep in attention-deficit/hyperactivity disorder in children and adults: past, present, and future Sleep Med Rev 16 371-388
  • [2] Jain U(2017)ADHD and sleep quality: longitudinal analyses from childhood to early adulthood in a twin cohort J Clin Child Adolesc Psychol 46 284-294
  • [3] Shapiro C(2017)Relationship between subtypes and symptoms of ADHD, insomnia, and nightmares in connection with quality of life in children Neuropsychiatr Dis Treat 13 2341-2350
  • [4] Gregory AM(2008)Sleep problems in children with attention-deficit/hyperactivity disorder: prevalence and the effect on the child and family Arch Pediatr Adolesc Med 162 336-342
  • [5] Agnew-Blais JC(2017)The role of sleep quality and quantity in moderating the effectiveness of medication in the treatment of children with ADHD Atten Defic Hyperact Disord 9 31-38
  • [6] Matthews T(2020)Sustained impact of a sleep intervention and moderators of treatment outcome for children with ADHD: a randomised controlled trial Psychol Med 50 210-219
  • [7] Grünwald J(2015)Impact of a behavioural sleep intervention on symptoms and sleep in children with attention deficit hyperactivity disorder, and parental mental health: randomised controlled trial BMJ 51 63-75
  • [8] Schlarb AA(2019)Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder Nat Genet 10 284-985
  • [9] Sung V(2020)Genetic associations between childhood psychopathology and adult depression and associated traits in 42 998 individuals: a meta-analysis JAMA Psychiat 11 187-502
  • [10] Hiscock H(2020)Polygenic risk score analysis revealed shared genetic background in attention deficit hyperactivity disorder and narcolepsy Transl Psychiatry 49 978-337