Kaufmann Walter E, Kidd Sharon A, Andrews Howard F, Budimirovic Dejan B, Esler Amy, Haas-Givler Barbara, Stackhouse Tracy, Riley Catharine, Peacock Georgina, Sherman Stephanie L, Brown W Ted, Berry-Kravis Elizabeth
Department of Neurology, Boston Children's Hospital, Boston, Massachusetts;
Greenwood Genetic Center, Greenwood, South Carolina.
Pediatrics. 2017 Jun;139(Suppl 3):S194-S206. doi: 10.1542/peds.2016-1159F.
Individuals with fragile X syndrome (FXS) are frequently codiagnosed with autism spectrum disorder (ASD). Most of our current knowledge about ASD in FXS comes from family surveys and small studies. The objective of this study was to examine the impact of the ASD diagnosis in a large clinic-based FXS population to better inform the care of people with FXS.
The study employed a data set populated by data from individuals with FXS seen at specialty clinics across the country. The data were collected by clinicians at the patient visit and by parent report for nonclinical and behavioral outcomes from September 7, 2012 through August 31, 2014. Data analyses were performed by using χ tests for association, tests, and multiple logistic regression to examine the association between clinical and other factors with ASD status.
Half of the males and nearly 20% of females met criteria for current ASD. Relative to the FXS-only group, the FXS with ASD (FXS+ASD) group had a higher prevalence of seizures (20.7% vs 7.6%, < .001), persistence of sleep problems later in childhood, increased behavior problems, especially aggressive/disruptive behavior, and higher use of α-agonists and antipsychotics. Behavioral services, including applied behavior analysis, appeared to be underused in children with FXS+ASD (only 26% and 16% in prekindergarten and school-age periods, respectively) relative to other populations with idiopathic ASD.
These findings confirm among individuals with FXS an association of an ASD diagnosis with important cooccurring conditions and identify gaps between expected and observed treatments among individuals with FXS+ASD.
脆性X综合征(FXS)患者常被共诊断为自闭症谱系障碍(ASD)。目前我们对FXS合并ASD的了解大多来自家庭调查和小型研究。本研究的目的是在一个大型的基于门诊的FXS人群中,检验ASD诊断的影响,以便更好地为FXS患者的护理提供信息。
本研究采用了一个数据集,该数据集由全国各地专科诊所中FXS患者的数据组成。数据于2012年9月7日至2014年8月31日期间,由临床医生在患者就诊时收集,并通过家长报告获取非临床和行为结果。数据分析采用χ²检验进行关联性分析、t检验以及多元逻辑回归,以检验临床因素和其他因素与ASD状态之间的关联。
一半的男性和近20%的女性符合当前ASD的标准。相对于仅患有FXS的组,患有FXS合并ASD(FXS+ASD)的组癫痫患病率更高(20.7%对7.6%,P<0.001),儿童期后期睡眠问题持续存在,行为问题增加,尤其是攻击性行为/破坏性行为,并且α-激动剂和抗精神病药物的使用频率更高。相对于其他特发性ASD人群,包括应用行为分析在内的行为服务在FXS+ASD儿童中似乎使用不足(学龄前和学龄期分别仅为26%和16%)。
这些发现证实了在FXS患者中,ASD诊断与重要共病情况之间的关联,并确定了FXS+ASD患者预期治疗与实际观察到的治疗之间的差距。