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. 2024 Aug 13.
doi: 10.1007/s10803-024-06512-1. Online ahead of print.

Genetic Diagnostic Yield in Autism Spectrum Disorder (ASD) and Epilepsy Phenotypes in Children with Genetically Defined ASD

Affiliations

Genetic Diagnostic Yield in Autism Spectrum Disorder (ASD) and Epilepsy Phenotypes in Children with Genetically Defined ASD

Karen Lob et al. J Autism Dev Disord. .

Abstract

We compared the epilepsy phenotypes in children with genetically defined versus undefined autism spectrum disorder (ASD). A single-center retrospective study was conducted to investigate diagnostic yields of different genetic testing for children with ASD. Patients with at least one testing modality were included and classified as having genetically defined ASD or not based on updated genotype-phenotype correlation. Of the 523 patients included, 79 (15.1%) had results explaining their ASD diagnosis. WES (whole exome sequencing) outperformed CMA (chromosomal microarray) on diagnostic yield (23.0% versus 8.3%). Compared to those with non-diagnostic test(s), children with genetically defined ASD were associated with higher rates for microcephaly, hypotonia, dysmorphic features, and developmental delay/regression. The prevalence of epilepsy was significantly higher in children with genetically defined ASD than those without a genetic diagnosis (35.4% versus 16.4%, p < 0.001, power = 0.97). Furthermore, children with genetically defined ASD had a younger age of epilepsy onset (median 2.2 versus 5.0 years, p = 0.002, power = 0.90) and a higher rate of drug-resistant epilepsy although not reaching statistical significance (35.7% versus 21.9%, p = 0.20). Our study has provided further evidence to support WES as first-tier test for children with ASD and that an early genetic diagnosis has the potential to inform further surveillance and management for ASD comorbid conditions including epilepsy.

Keywords: Autism; Epilepsy; Genetic; Neurodevelopmental disorder; Pediatric.

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References

    1. American Psychiatric Association. (2020). Diagnostic and statistical manual of mental disorders (5th ed.). American Psychiatric Association.
    1. Arteche-Lopez, A., Gomez Rodriguez, M. J., Sanchez Calvin, M. T., Quesada-Espinosa, J. F., Lezana Rosales, J. M., Palma Milla, C., Gomez-Manjon, I., Hidalgo Mayoral, I., Perez de la Fuente, R., Diaz de Bustamante, A., Darnaude, M. T., Gil-Fournier, B., Ramiro Leon, S., Ramos Gomez, P., Sierra Tomillo, O., Juarez Rufian, A., Arranz Cano, M. I., Villares Alonso, R., Morales-Perez, P., … Alvarez-Mora, M. I. (2021). Towards a change in the diagnostic algorithm of autism spectrum disorders: Evidence supporting whole exome sequencing as a first-tier test. Genes (basel). https://doi.org/10.3390/genes12040560 - DOI - PubMed
    1. Christensen, D. L., Braun, K. V. N., Baio, J., Bilder, D., Charles, J., Constantino, J. N., Daniels, J., Durkin, M. S., Fitzgerald, R. T., Kurzius-Spencer, M., Lee, L. C., Pettygrove, S., Robinson, C., Schulz, E., Wells, C., Wingate, M. S., Zahorodny, W., & Yeargin-Allsopp, M. (2018). Prevalence and characteristics of autism spectrum disorder among children aged 8 years—Autism and developmental disabilities monitoring network, 11 sites, United States, 2012. MMWR Surveillance Summaries, 65(13), 1–23. https://doi.org/10.15585/mmwr.ss6513a1 - DOI - PMC
    1. Chu-Shore, C. J., Major, P., Camposano, S., Muzykewicz, D., & Thiele, E. A. (2010). The natural history of epilepsy in tuberous sclerosis complex. Epilepsia, 51(7), 1236–1241. https://doi.org/10.1111/j.1528-1167.2009.02474.x - DOI - PubMed
    1. D’Mello, A. M., Frosch, I. R., Li, C. E., Cardinaux, A. L., & Gabrieli, J. D. E. (2022). Exclusion of females in autism research: Empirical evidence for a “leaky” recruitment-to-research pipeline. Autism Research, 15(10), 1929–1940. https://doi.org/10.1002/aur.2795 - DOI - PubMed - PMC

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