3q29缺失综合征个体的自闭症谱系障碍症状表达

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY
Rebecca M Pollak, Jordan E Pincus, T Lindsey Burrell, Joseph F Cubells, Cheryl Klaiman, Melissa M Murphy, Celine A Saulnier, Elaine F Walker, Stormi Pulver White, Jennifer G Mulle
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引用次数: 1

摘要

背景:1.6 Mb 3q29缺失与神经发育和神经精神表型相关,包括自闭症谱系障碍(ASD)风险增加19倍。我们团队之前的工作通过父母报告问卷确定了这一人群中社会残疾的增加。然而,该人群ASD的临床特征尚未得到详细探讨。方法:对31例3q29缺失综合征(3q29del, 61.3%男性)患者进行两种金标准的ASD临床评估:自闭症诊断观察表第二版(ADOS-2)和自闭症诊断访谈(ADI-R)。从国家自闭症研究数据库中为每个受试者确定了四个匹配的比较物。比较具有3q29del和匹配比较物的受试者的ADOS-2和ADI-R的项目水平得分。结果:在ADOS-2中,3q29del和无ASD (3q29del-ASD)的受试者比典型发育(TD)的对照组有更大的社会残疾证据。在ADOS-2上,3q29del和ASD (3q29del + ASD)受试者与非综合征性ASD (nsASD)受试者在很大程度上无法区分。3q29del + ASD在ADI-R上的社交沟通表现明显优于nsASD (3q29 + ASD平均值= 11.36;nsASD平均值= 15.70;p = 0.01),这是由于非语言交流缺陷减少所致(3q29 + ASD平均值= 1.73;nsASD均值= 3.63;p = 0.03)。与非ASD相比,3q29del + ASD在第一个双字短语时的年龄明显晚于3q29del + ASD (3q29del + ASD平均= 43.89个月;nsASD平均= 37.86个月;p = 0.01)。然而,在3q29del + ASD中,言语延迟与非语言交际的改善无关。局限性:在NDAR中没有足够的TD比较物与ADI-R数据纳入本分析。此外,我们相对较小的样本量使得很难评估种族和民族的影响。结论:与ASD诊断无关,3q29del与显著的社交障碍相关。3q29del + ASD与非ASD具有相似的社会残疾水平,而3q29del-ASD与TD个体相比具有显著增加的社会残疾。然而,相对于非ASD, 3q29del + ASD患者的社交沟通得到了相当好的保存。在这一人群中,语言能力和社会残疾必须分开检查,以确保有平等的机会获得ASD和社会技能评估和服务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome.

Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome.

Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome.

Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome.

Background: The 1.6 Mb 3q29 deletion is associated with neurodevelopmental and neuropsychiatric phenotypes, including a 19-fold increased risk for autism spectrum disorder (ASD). Previous work by our team identified elevated social disability in this population via parent-report questionnaires. However, clinical features of ASD in this population have not been explored in detail.

Methods: Thirty-one individuals with 3q29 deletion syndrome (3q29del, 61.3% male) were evaluated using two gold-standard clinical ASD evaluations: the Autism Diagnostic Observation Schedule, Second Edition (ADOS-2), and the Autism Diagnostic Interview, Revised (ADI-R). Four matched comparators for each subject were ascertained from the National Database for Autism Research. Item-level scores on the ADOS-2 and ADI-R were compared between subjects with 3q29del and matched comparators.

Results: Subjects with 3q29del and no ASD (3q29del-ASD) had greater evidence of social disability compared to typically developing (TD) comparison subjects across the ADOS-2. Subjects with 3q29del and ASD (3q29del + ASD) were largely indistinguishable from non-syndromic ASD (nsASD) subjects on the ADOS-2. 3q29del + ASD performed significantly better on social communication on the ADI-R than nsASD (3q29 + ASD mean = 11.36; nsASD mean = 15.70; p = 0.01), and this was driven by reduced deficits in nonverbal communication (3q29 + ASD mean = 1.73; nsASD mean = 3.63; p = 0.03). 3q29del + ASD reported significantly later age at the first two-word phrase compared to nsASD (3q29del + ASD mean = 43.89 months; nsASD mean = 37.86 months; p = 0.01). However, speech delay was not related to improved nonverbal communication in 3q29del + ASD.

Limitations: There were not enough TD comparators with ADI-R data in NDAR to include in the present analysis. Additionally, our relatively small sample size made it difficult to assess race and ethnicity effects.

Conclusions: 3q29del is associated with significant social disability, irrespective of ASD diagnosis. 3q29del + ASD have similar levels of social disability to nsASD, while 3q29del-ASD have significantly increased social disability compared to TD individuals. However, social communication is reasonably well preserved in 3q29del + ASD relative to nsASD. It is critical that verbal ability and social disability be examined separately in this population to ensure equal access to ASD and social skills evaluations and services.

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来源期刊
Molecular Autism
Molecular Autism GENETICS & HEREDITY-NEUROSCIENCES
CiteScore
12.10
自引率
1.60%
发文量
44
审稿时长
17 weeks
期刊介绍: Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
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