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Maria Niarchou, Emily V. Singer, Peter Straub, Beth A. Malow, Lea K. Davis (2022). Investigating the genetic pathways of insomnia in Autism Spectrum Disorder. openRxiv.

Date de publication
04/02/2022
Identifiant
10.1101/2022.02.03.22270340
Auteurs
Maria Niarchou, Emily V. Singer, Peter Straub, Beth A. Malow, Lea K. Davis
Type de référence
preprint
Éditeur
openRxiv
Source de métadonnées
crossref

Résumé

Abstract Background Sleep problems are common in children with autism spectrum disorder (autism). There is sparse research to date to examine whether insomnia in people with autism is related to autism genetics or insomnia genetics. Moreover, there is a lack of research examining whether circadian-rhythm related genes share potential pathways with autism. Aims To address this research gap, we tested whether polygenic scores of insomnia or autism are related to risk of insomnia in people with autism, and to test whether the circadian genes are associated with insomnia in people with autism. Methods and procedures We tested these questions using the phenotypically and genotypically rich MSSNG dataset (N=1,049) as well as incorporating in the analyses data from the Vanderbilt University Biobank (BioVU) (N=349). Outcomes and results In our meta-analyzed sample, there was no evidence of associations between the polygenic scores (PGS) for insomnia and a clinical diagnosis of insomnia, or between the PGS of autism and insomnia. We also did not find evidence of a greater burden of rare and disruptive variation in the melatonin and circadian genes in individuals with autism and insomnia compared to individuals with autism without insomnia. Conclusions and implications Overall, we did not find evidence for strong effects of genetic scores influencing sleep in people with autism, however, we cannot rule out the possibility that smaller genetic effects may play a role in sleep problems. Our study indicated the need for a larger collection of data on sleep problems and sleep quality among people with autism.

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