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Etiological links between autism and difficulties in initiating and maintaining sleep

A familial co‐aggregation and twin study

Bibliographic Data

ID21344229
AuthorsMark J Taylor (0000-0001-5161-4182, Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden, corresponding author), Henrik Larsson (0000-0002-6851-3297, Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden), Sven Lundstrom (0000-0001-7235-8499, University of Gothenburg), Sebastian Lundstrom (Gillberg Neuropsychiatry Centre University of Gothenburg Gothenburg Sweden), Paul Lichtenstein (0000-0003-3037-5287, Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden), Agnieszka Butwicka (0000-0002-7247-2141, Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden)
Year2022
Volume63
Issue3
Pages315-323
Publication date2022-03-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueJournal of Child Psychology and Psychiatry (JOURNAL)
Journal identifiersISSN: 0021-9630 • E-ISSN: 1469-7610
PublisherWiley (PUBLISHER • GB)
DOI10.1111/jcpp.13473
PMID34213012
OpenAlexW3173586423
LanguageEN
Citations received1
References cited42

BACKGROUND: Difficulties initiating and maintaining sleep (DIMS) are frequent features of autism, yet little is known about why these conditions co-occur. One possibility is that they share etiological factors, yet this hypothesis remains to be tested using quantitative genetic designs. We thus investigated etiological links between autism and DIMS using familial co-aggregation and twin methods. METHODS: Twins, siblings, half-siblings, and cousins of 50,097 individuals with autism were identified from Swedish population registries. Their risk of DIMS, defined through diagnoses of insomnia and/or melatonin prescriptions, was then estimated. Twin analyses conducted on 15,279 child and adolescent twin pairs investigated etiological links between DIMS and ASD. RESULTS: 22.8% of autistic individuals had DIMS. Monozygotic co-twins of individuals with autism were most at risk of DIMS compared to the reference group (OR = 6.6 [2.5-17.4]), followed by dizygotic co-twins (OR = 2.6 [1.5-4.5]) and full siblings (OR = 2.5 [2.4-2.6]). Half-siblings and cousins of individuals with autism were least likely to have DIMS relative to the reference group (OR range = 1.3-1.5). Twin analyses estimated a correlation of 0.57 (0.53-0.61) between autism and DIMS, with a genetic correlation of 0.62 (0.60-0.68). These overlapping genetic factors explained 94% of the covariance between these conditions. Autistic traits also showed genetic overlap with DIMS. CONCLUSIONS: Our results suggest that shared genetic mechanisms underlie autism and DIMS, which may lead them to co-occur. Untangling the etiological overlap between these conditions has potential to assist in understanding the etiology of each condition, as well as their associated outcomes

Autism · Autism spectrum disorder · Biology · Developmental disorder · Developmental psychology · Etiology · Family aggregation · Heritability · Heritability of autism · Population · Psychiatry · Twin study · Autism Spectrum Disorder Research · Child Nutrition and Feeding Issues · Clinical Psychology · Genetics · Medicine · Psychology · Sleep and related disorders

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    Pasquale K Alvaro, Rachel M Roberts et al.•Sleep•2013

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    Open Access•John Grove, BUPGEN BUPGEN et al.•Nature Genetics•2019

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Unique citing works1
Citations per year1
Citation span2025 - 2025 (1)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 1

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