Xie Sherlly, Karlsson Håkan, Dalman Christina, Widman Linnea, Rai Dheeraj, Gardner Renee M, Magnusson Cecilia, Sandin Sven, Tabb Loni P, Newschaffer Craig J, Lee Brian K
Department of Epidemiology and Biostatistics, Drexel University School of Public Health, Philadelphia, Pennsylvania, USA.
Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Autism Res. 2020 Dec;13(12):2242-2250. doi: 10.1002/aur.2417. Epub 2020 Oct 26.
Autism spectrum disorder (ASD) is highly heritable, yet how its familial risk and heritability may vary by cognitive ability is not well understood. In this population-based cohort study, we examined the familial risk and heritability of ASD with and without co-occurring intellectual disability (ID). We estimated odds ratios and heritability of ASD with ID (ASD+ID) and ASD without ID (ASD-ID) using register-based diagnosis data of 567,436 index persons born in 1984-2009 in Stockholm County, Sweden, and their parents, siblings, cousins, aunts, and uncles. The familial risk profile exhibited differences between ASD-ID and ASD+ID, most notably for index persons with affected parents. For example, for an index person who had at least one parent with ASD, the child's odds of ASD-ID and ASD+ID (95% confidence interval (CI)) increased by 16.2 (14.2-18.6) and 7.4 (5.5-10.0) folds, respectively. The more closely related a family member with ASD was, the greater the observed risk was of ASD in the index person, especially for ASD-ID. The broad-sense heritability (95% CI) for ASD - ID and ASD+ID were 64.6% (46.0-100.0%) and 33.4% (14.4-58.4%), respectively. Familial risk and heritability of ASD may vary by intellectual ability, which implies that risk factors between these ASD phenotypes may differ. Our findings from the heritability analysis and familial risk analysis suggest that ASD-ID may have a greater genetic basis than ASD+ID, although this should be verified in future studies. LAY SUMMARY: Autism spectrum disorder (ASD) is highly heritable, yet how its familial risk and heritability may vary by cognitive ability is not well-understood. In a population-based cohort study on families of 567,436 index persons using Swedish registers data, we found that the familial risk profile differed between ASD with and without intellectual disability. Our findings from the heritability analysis and familial risk analysis suggest that ASD-ID may have a greater genetic basis than ASD+ID, although this should be verified in future studies.
自闭症谱系障碍(ASD)具有高度遗传性,但其家族风险和遗传力如何因认知能力而异,目前尚不清楚。在这项基于人群的队列研究中,我们研究了伴有和不伴有智力残疾(ID)的ASD的家族风险和遗传力。我们使用瑞典斯德哥尔摩县1984年至2009年出生的567,436名索引人群及其父母、兄弟姐妹、堂兄弟姐妹、姑姑和叔叔的基于登记的诊断数据,估计了伴有ID的ASD(ASD+ID)和不伴有ID的ASD(ASD-ID)的比值比和遗传力。家族风险概况在ASD-ID和ASD+ID之间表现出差异,对于有患病父母的索引人群尤为明显。例如,对于至少有一位患有ASD的父母的索引人群,其患ASD-ID和ASD+ID(95%置信区间(CI))的几率分别增加了16.2(14.2-18.6)倍和7.4(5.5-10.0)倍。患有ASD的家庭成员关系越密切,索引人群患ASD的风险就越高,尤其是对于ASD-ID。ASD-ID和ASD+ID的广义遗传力(95%CI)分别为64.6%(46.0-100.0%)和33.4%(14.4-58.4%)。ASD的家族风险和遗传力可能因智力能力而异,这意味着这些ASD表型之间的风险因素可能不同。我们从遗传力分析和家族风险分析中得出的结果表明,ASD-ID可能比ASD+ID具有更大的遗传基础,尽管这一点应在未来的研究中得到验证。简要概述:自闭症谱系障碍(ASD)具有高度遗传性,但其家族风险和遗传力如何因认知能力而异,目前尚不清楚。在一项基于人群的队列研究中,我们使用瑞典登记数据对567,