Preprint
Genomic dissection of sleep archetypes in a large autism cohort
medRxiv
Cold Spring Harbor Laboratory Press, 1.1
04/06/2025
DOI: 10.1101/2025.04.04.25325272
PMCID: PMC11998819
PMID: 40236407
Abstract
Poor sleep is a major concern among individuals with autism and their caregivers. To better characterize the genetic and phenotypic heterogeneity of poor sleep in autism, we recruited 5,686 families from SPARK, a nationwide genetic study of autism, who described their sleep experiences using the Children’s Sleep Health Questionnaire (CSHQ) and other self-report items. The collective experiences from this large sample allowed us to discover eight distinct archetypes of sleep in autism. Membership in some of these archetypes showed significant SNP-heritability (0.50 - 0.65, 95% confidence interval = 0.08 - 1), and polygenic estimates of educational attainment, BMI, and ADHD risk contributed extensively to the genetic signatures of these sleep archetypes. Surprisingly, polygenic estimates of general population sleep phenotypes showed sparser and more modest associations, perhaps suggesting that the genetic drivers of disordered sleep in autism may be distinct from those encountered in the general population. GWAS on archetype membership yielded no genome-wide significant loci, however, the most significant gene for the most severe archetype was the nitric oxide (NO) signaling gene NOS1AP, which was previously linked to sleep disruption in schizophrenia. Finally, the eight sleep archetypes showed specific signatures of treatment response across five major categories of sleep aid, pointing to the potential of treatment plans that are tailored to the nature of the sleep problem. These findings provide critical new insight into the comorbidities, subtypes, and genetic risk factors associated with disordered sleep in autism.
Details
- Title: Subtitle
- Genomic dissection of sleep archetypes in a large autism cohort
- Creators
- Leo Brueggeman - Department of Psychiatry, University of IowaNatalie Pottschmidt - Pennsylvania State UniversityTanner Koomar - University of IowaTaylor Thomas - University of IowaJacob J. Michaelson - Department of Psychiatry, University of Iowa
- Resource Type
- Preprint
- Publication Details
- medRxiv
- Edition
- 1.1
- DOI
- 10.1101/2025.04.04.25325272
- PMID
- 40236407
- PMCID
- PMC11998819
- Publisher
- Cold Spring Harbor Laboratory Press
- Number of pages
- 26
- Language
- English
- Date posted
- 04/06/2025
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Communication Sciences and Disorders; Psychiatry; Iowa Neuroscience Institute
- Record Identifier
- 9984810949102771
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