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自闭症谱系障碍和注意缺陷多动障碍的家族共聚集:基于登记的队列研究。

The familial co-aggregation of ASD and ADHD: a register-based cohort study.

机构信息

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.

出版信息

Mol Psychiatry. 2018 Feb;23(2):257-262. doi: 10.1038/mp.2017.17. Epub 2017 Feb 28.

Abstract

Autism spectrum disorders (ASD) and attention-deficit/hyperactivity disorder (ADHD) frequently co-occur. The presence of a genetic link between ASD and ADHD symptoms is supported by twin studies, but the genetic overlap between clinically ascertained ASD and ADHD remains largely unclear. We therefore investigated how ASD and ADHD co-aggregate in individuals and in families to test for the presence of a shared genetic liability and examined potential differences between low- and high-functioning ASD in the link with ADHD. We studied 1 899 654 individuals born in Sweden between 1987 and 2006. Logistic regression was used to estimate the association between clinically ascertained ASD and ADHD in individuals and in families. Stratified estimates were obtained for ASD with (low-functioning) and without (high-functioning) intellectual disability. Individuals with ASD were at higher risk of having ADHD compared with individuals who did not have ASD (odds ratio (OR)=22.33, 95% confidence interval (CI): 21.77-22.92). The association was stronger for high-functioning than for low-functioning ASD. Relatives of individuals with ASD were at higher risk of ADHD compared with relatives of individuals without ASD. The association was stronger in monozygotic twins (OR=17.77, 95% CI: 9.80-32.22) than in dizygotic twins (OR=4.33, 95% CI: 3.21-5.85) and full siblings (OR=4.59, 95% CI: 4.39-4.80). Individuals with ASD and their relatives are at increased risk of ADHD. The pattern of association across different types of relatives supports the existence of genetic overlap between clinically ascertained ASD and ADHD, suggesting that genomic studies might have underestimated this overlap.

摘要

自闭症谱系障碍(ASD)和注意缺陷/多动障碍(ADHD)经常同时发生。双胞胎研究支持 ASD 和 ADHD 症状之间存在遗传联系,但临床上确定的 ASD 和 ADHD 之间的遗传重叠在很大程度上仍不清楚。因此,我们研究了 ASD 和 ADHD 在个体和家庭中的共同聚集程度,以检验是否存在共同的遗传易感性,并检查低功能和高功能 ASD 与 ADHD 之间的联系是否存在差异。我们研究了 1899654 名 1987 年至 2006 年期间出生于瑞典的个体。使用逻辑回归来估计临床上确定的 ASD 和 ADHD 在个体和家庭中的关联。对于具有(低功能)和不具有(高功能)智力障碍的 ASD 进行分层估计。与没有 ASD 的个体相比,患有 ASD 的个体患 ADHD 的风险更高(优势比(OR)=22.33,95%置信区间(CI):21.77-22.92)。高功能 ASD 比低功能 ASD 的关联更强。患有 ASD 的个体的亲属患 ADHD 的风险高于没有 ASD 的个体的亲属。同卵双胞胎(OR=17.77,95%CI:9.80-32.22)的关联强于异卵双胞胎(OR=4.33,95%CI:3.21-5.85)和全同胞(OR=4.59,95%CI:4.39-4.80)。患有 ASD 的个体及其亲属患 ADHD 的风险增加。不同类型亲属之间的关联模式支持临床上确定的 ASD 和 ADHD 之间存在遗传重叠,这表明基因组研究可能低估了这种重叠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72f1/5794881/cf366daa4737/mp201717f1.jpg

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