A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

Alexander S. F. Berry, Brenda M. Finucane, Scott M. Myers, Lauren K. Walsh, John M. Seibert, Christa Lese Martin, David H. Ledbetter and Matthew T. Oetjens ()
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Alexander S. F. Berry: Geisinger
Brenda M. Finucane: Geisinger
Scott M. Myers: Geisinger
Lauren K. Walsh: Geisinger
John M. Seibert: Geisinger
Christa Lese Martin: Geisinger
David H. Ledbetter: University of Florida College of Medicine
Matthew T. Oetjens: Geisinger

Nature Communications, 2024, vol. 15, issue 1, 1-11

Abstract: Abstract A female protective effect has long been postulated as the primary explanation for the four-fold increase of autism spectrum disorder (ASD) diagnoses in males versus females. However, genetic and epidemiological investigations of this hypothesis have so far failed to explain the large difference in ASD prevalence between the sexes. To address this knowledge gap, we examined sex chromosome aneuploidy in a large ASD case-control cohort to evaluate the relationship between X and Y chromosome dosage and ASD risk. From these data, we modeled three relationships between sex chromosome dosage and ASD risk: the extra Y effect, the extra X effect, and sex chromosome haploinsufficiency. We found that the extra Y effect increased ASD risk significantly more than the extra X effect. Among females, we observed a large association between 45, X and ASD, confirming sex chromosome haploinsufficiency as a strong ASD risk factor. These results provide a framework for understanding the relationship between X and Y chromosome dosage on ASD, which may inform future research investigating genomic contributors to the observed sex difference.

Date: 2024
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DOI: 10.1038/s41467-024-53211-7

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