Department of Psychiatry, Carolina Institute for Developmental Disabilities, University of North Carolina School of Medicine, 101 Renee Lynne Court, Carrboro, NC, 27510, USA.
Department of Pediatrics, Marcus Autism Center, Emory University School of Medicine, Atlanta, USA.
Neuropsychopharmacology. 2018 Jul;43(8):1772-1778. doi: 10.1038/s41386-018-0039-3. Epub 2018 Feb 27.
In a prior report, we showed that extended-release guanfacine (GEXR) is safe and effective for children with autism spectrum disorder (ASD) accompanied by ADHD symptoms. Here, we examine the impact of GEXR on oppositional behavior, anxiety, repetitive behavior, and sleep disturbance. Sixty-two subjects with ASD (53 boys, 9 girls; ages 5-14 years) were randomly assigned to GEXR (n = 30) or placebo (n = 32) for 8 weeks. Outcomes include the Home Situation Questionnaire-Modified for ASD (HSQ-ASD), Anxiety scale of the Child and Adolescent Symptom Inventory (CASI), Children's Yale-Brown Obsessive-Compulsive Scale-Modified for ASD (CYBOCS-ASD), and Children's Sleep Habits Questionnaire (CSHQ). A repeated measures linear mixed model was used to determine the effects of treatment group and time on HSQ scores. For other measures, change from baseline was evaluated with Analysis of Covariance (ANCOVA).After 8 weeks of treatment, parent ratings of oppositional behavior on the HSQ declined by 44% (per item mean from 3.4 to 1.9) in the GEXR group compared to 12% (from 3.3 to 2.9) for placebo (p = 0.004). Repetitive behavior on the CYBOCS-ASD showed a significantly greater decline in GEXR-treated participants compared to placebo (24% vs. <1%, p = 0.01). No group differences were observed on CASI Anxiety or CSHQ (p = 0.64 and 0.75, respectively). GEXR was effective in reducing oppositional behavior and, more modestly, repetitive behavior. GEXR was not superior to placebo for anxiety, though baseline anxiety ratings were low. GEXR did not significantly improve sleep habits. Future studies could focus on repetitive behavior or anxiety, symptoms with limited treatment options.
在之前的报告中,我们表明,延长释放胍法辛(GEXR)对伴有 ADHD 症状的自闭症谱系障碍(ASD)儿童是安全有效的。在这里,我们研究了 GEXR 对对立行为、焦虑、重复行为和睡眠障碍的影响。62 名 ASD 儿童(53 名男孩,9 名女孩;年龄 5-14 岁)被随机分配到 GEXR(n=30)或安慰剂(n=32)治疗 8 周。结果包括自闭症家庭情况问卷(HSQ-ASD)、儿童和青少年症状清单焦虑量表(CASI)、儿童耶鲁布朗强迫症量表-自闭症修订版(CYBOCS-ASD)和儿童睡眠习惯问卷(CSHQ)。采用重复测量线性混合模型来确定治疗组和时间对 HSQ 评分的影响。对于其他指标,采用协方差分析(ANCOVA)评估从基线的变化。经过 8 周的治疗,GEXR 组的父母对 HSQ 中对立行为的评分下降了 44%(每项平均从 3.4 降至 1.9),而安慰剂组下降了 12%(从 3.3 降至 2.9)(p=0.004)。CYBOCS-ASD 上的重复行为在 GEXR 治疗组中显示出比安慰剂组更大的下降(24%比<1%,p=0.01)。在 CASI 焦虑或 CSHQ 上,两组间没有差异(分别为 p=0.64 和 0.75)。GEXR 可有效减少对立行为,更适度地减少重复行为。GEXR 对焦虑的疗效并不优于安慰剂,尽管基线焦虑评分较低。GEXR 对睡眠习惯没有显著改善。未来的研究可以集中在重复行为或焦虑上,这些症状的治疗选择有限。