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自闭症儿童的精神疾病家族史及兄弟姐妹的发育情况。

Family history of psychiatric conditions and development of siblings of children with autism.

作者信息

Bellia Giselle, Chang Joseph, Liew Zeyan, Vernetti Angelina, Macari Suzanne, Powell Kelly, Chawarska Katarzyna

机构信息

Yale Center for Perinatal, Pediatric and Environmental Epidemiology, Yale School of Public Health, New Haven, Connecticut, USA.

Department of Statistics and Data Science, Yale University, New Haven, Connecticut, USA.

出版信息

Autism Res. 2024 Aug;17(8):1665-1676. doi: 10.1002/aur.3175. Epub 2024 Jun 19.

Abstract

Younger siblings (SIBS) of children with autism exhibit a wide range of clinical and subclinical symptoms including social, cognitive, language, and adaptive functioning delays. Identifying factors linked with this phenotypic heterogeneity is essential for improving understanding of the underlying biology of the heterogenous outcomes and for early identification of the most vulnerable SIBS. Prevalence of neurodevelopmental (NDD) and neuropsychiatric disorders (NPD) is significantly elevated in families of children with autism. It remains unknown, however, if the family history associates with the developmental outcomes among the SIBS. We quantified history of the NDDs and NPDs commonly reported in families of children with autism using a parent interview and assessed autism symptoms, verbal, nonverbal, and adaptive skills in a sample of 229 SIBS. Multiple regression analyses were used to examine links between family history and phenotypic outcomes, whereas controlling for birth year, age, sex, demographics, and parental education. Results suggest that family history of schizophrenia, depression, anxiety, bipolar disorder, and intellectual disability associate robustly with dimensional measures of social affect, verbal and nonverbal IQ, and adaptive functioning in the SIBS. Considering family history of these disorders may improve efforts to predict long-term outcomes in younger siblings of children with autism and inform about familial factors contributing to high phenotypic heterogenetity in this cohort.

摘要

自闭症儿童的弟弟妹妹(手足)表现出广泛的临床和亚临床症状,包括社交、认知、语言和适应性功能发育迟缓。确定与这种表型异质性相关的因素,对于增进对异质性结果潜在生物学机制的理解以及早期识别最易受影响的手足至关重要。自闭症儿童家庭中神经发育障碍(NDD)和神经精神疾病(NPD)的患病率显著升高。然而,家族病史是否与手足的发育结果相关仍不清楚。我们通过家长访谈对自闭症儿童家庭中常见的NDD和NPD病史进行了量化,并在229名手足样本中评估了自闭症症状、语言、非语言和适应性技能。多元回归分析用于检验家族病史与表型结果之间的联系,同时控制出生年份、年龄、性别、人口统计学特征和父母教育程度。结果表明,精神分裂症、抑郁症、焦虑症、双相情感障碍和智力残疾的家族病史与手足的社会情感、语言和非语言智商以及适应性功能的维度测量密切相关。考虑这些疾病的家族病史可能有助于改善对自闭症儿童弟弟妹妹长期结果的预测,并了解导致该队列中高表型异质性的家族因素。

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