Department of Psychiatry, The Hospital for Sick Children, Toronto, ON, Canada.
Department of Psychiatry, The University of Toronto, Toronto, ON, Canada.
Eur J Hum Genet. 2022 Nov;30(11):1297-1300. doi: 10.1038/s41431-022-01181-z. Epub 2022 Sep 6.
In children undergoing genetic testing for physical health concerns, we examined how often the results also revealed information about their risk for neurodevelopmental disorders. The study sample consisted of 3056 genetic tests (1686 chromosomal microarrays--CMAs, and 1378 next-generation sequencing--NGS panels) ordered at a tertiary pediatric hospital because of a physical/congenital health problem. Tests ordered to investigate developmental concerns were excluded. Pathogenic, or likely pathogenic variants were manually reviewed for diagnostic likelihood, and for evidence of an association with a neurodevelopmental disorder (e.g., autism or intellectual disability). A total of 169 CMAs (10%) and 232 NGS panels (17%) had likely diagnostic results. More than half (52%) of all diagnostic results had established evidence of a neurodevelopmental disorder association. In summary, there is a high prevalence of neurodevelopmental implications from genetic tests ordered for physical/congenital indications. This broad clinical utility suggests a growing need for genetics-first developmental care pathways.
在为身体健康问题接受基因检测的儿童中,我们研究了检测结果揭示其神经发育障碍风险信息的频率。研究样本包括在一家三级儿科医院因身体/先天健康问题而进行的 3056 项基因检测(1686 项染色体微阵列-CMA 和 1378 项下一代测序-NGS 面板)。排除了为研究发育问题而进行的检测。对致病性或可能致病性变体进行手动审查,以评估其诊断可能性,以及与神经发育障碍(例如自闭症或智力残疾)的关联证据。共有 169 项 CMA(10%)和 232 项 NGS 面板(17%)具有可能的诊断结果。所有诊断结果中有一半以上(52%)有明确的神经发育障碍关联证据。总之,为身体/先天指征而进行的基因检测存在较高的神经发育影响的普遍性。这种广泛的临床应用表明,需要建立以遗传学为基础的发展护理途径。