自闭症
队列
基因检测
遗传综合征
医学
队列研究
心理学
精神科
遗传学
临床心理学
儿科
生物
内科学
作者
Jessica R. Wright,Irina Astrovskaya,Sarah D. Barns,Alexandra Goler,Xueya Zhou,Chang Shu,LeeAnne Green Snyder,Bing Han,Alexandria Aarrestad,Leonard Abbeduto,Gabriella Aberbach,Shelley Aberle,Adediwura Adegbite,Debbie Adeniji,Maria Aguilar,Kaitlyn Ahlers,Charles Albright,Michael Alessandri,Zach Algaze,Jasem Alkazi
标识
DOI:10.1016/j.gim.2024.101202
摘要
PURPOSE: The aim of this study is to identify likely pathogenic (LP) and pathogenic (P) genetic results for autism that can be returned to participants in SPARK (SPARKforAutism.org): a large recontactable cohort of people with autism in the United States. We also describe the process to return these clinically confirmed genetic findings. METHODS: We present results from microarray genotyping and exome sequencing of 21,532 individuals with autism and 17,785 of their parents. We returned LP and P (American College of Medical Genetics criteria) copy-number variants, chromosomal aneuploidies, and variants in genes with strong evidence of association with autism and intellectual disability. RESULTS: We identified 1903 returnable LP/P variants in 1861 individuals with autism (8.6%). 89.5% of these variants were not known to participants. The diagnostic genetic result was returned to 589 participants (53% of those contacted). Features associated with a higher probability of having a returnable result include cognitive and medically complex features, being female, being White (versus non-White) and being diagnosed more than 20 years ago. We also find results among autistics across the spectrum, as well as in transmitting parents with neuropsychiatric features but no autism diagnosis. CONCLUSION: SPARK offers an opportunity to assess returnable results among autistic people who have not been ascertained clinically. SPARK also provides practical experience returning genetic results for a behavioral condition at a large scale.
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