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美国发育障碍儿童家长的基因归因相关因素。

Correlates of genetic attributions among parents of children in the USA with developmental disabilities.

作者信息

Kiely Bridget, Vettam Sujit, Adesman Andrew

机构信息

Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, Steven and Alexandra Cohen Children's Medical Center of New York, New Hyde Park, NY, USA,

出版信息

Appl Clin Genet. 2019 Apr 12;12:55-61. doi: 10.2147/TACG.S164757. eCollection 2019.

Abstract

INTRODUCTION

As technologies for identifying causal genetic variants in children with autism spectrum disorders (ASD) and other developmental conditions continue to advance, there is a need to understand the factors that influence parental beliefs about the causes of their child's disabilities. This study assessed the correlates of etiologic attributions among US parents of children with ASD, intellectual disability (ID), and/or developmental delay (DD).

METHODS

Data were obtained from the Centers for Disease Control and Prevention's nationally representative Survey of Pathways to Diagnosis and Services. Respondents were classified according to whether their child had ASD without ID or DD (ASD-only), ASD with ID and/or DD (ASD+ID/DD), or ID and/or DD without ASD (ID/DD-only). Respondents rated the extent to which they believed that genetics/heredity and environmental exposures (prenatal and/or postnatal) had contributed to their child's condition. Logistic regression analyses and chi-square tests were used to assess the relationship between parental beliefs and child characteristics.

RESULTS

The parents of children with comorbid ASD and ID/DD were found to be significantly less likely than those in the other condition groups to attribute their child's condition to genetics. Within the ASD+ID/DD group, parental endorsement of genetics was lower among those who reported a history of language regression (=0.006).

CONCLUSION

Further research is needed to evaluate the impact of parental genetic attributions on medical decision-making.

摘要

引言

随着用于识别自闭症谱系障碍(ASD)及其他发育障碍儿童因果基因变异的技术不断进步,有必要了解影响父母对孩子残疾原因看法的因素。本研究评估了美国患有ASD、智力残疾(ID)和/或发育迟缓(DD)儿童的父母病因归因的相关因素。

方法

数据来自疾病控制与预防中心具有全国代表性的诊断与服务途径调查。受访者根据其孩子是否患有无ID或DD的ASD(仅ASD)、患有ID和/或DD的ASD(ASD+ID/DD)或无ASD的ID和/或DD(仅ID/DD)进行分类。受访者对他们认为基因/遗传和环境暴露(产前和/或产后)对孩子病情影响程度进行评分。采用逻辑回归分析和卡方检验来评估父母看法与孩子特征之间的关系。

结果

发现患有ASD合并ID/DD的儿童的父母比其他病情组的父母将孩子的病情归因于基因的可能性显著降低。在ASD+ID/DD组中,报告有语言倒退史的父母对基因的认同度较低(P=0.006)。

结论

需要进一步研究来评估父母基因归因对医疗决策的影响。

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