Potter Laura A, Scholze Danielle A, Biag Hazel Maridith B, Schneider Andrea, Chen Yanjun, Nguyen Danh V, Rajaratnam Akash, Rivera Susan M, Dwyer Patrick S, Tassone Flora, Al Olaby Reem R, Choudhary Nimrah S, Salcedo-Arellano Maria J, Hagerman Randi J
Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, UC Davis Health, Sacramento, CA, United States.
Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Front Psychiatry. 2019 Nov 6;10:810. doi: 10.3389/fpsyt.2019.00810. eCollection 2019.
Selective serotonin reuptake inhibitors like sertraline have been shown in observational studies and anecdotal reports to improve language development in young children with fragile X syndrome (FXS). A previous controlled trial of sertraline in young children with FXS found significant improvement in expressive language development as measured by the Mullen Scales of Early Learning (MSEL) among those with comorbid autism spectrum disorder (ASD) in analysis, prompting the authors to probe whether sertraline is also indicated in nonsyndromic ASD. The authors evaluated the efficacy of 6 months of treatment with low-dose sertraline in a randomized, double-blind, placebo-controlled trial in 58 children with ASD aged 24 to 72 months. 179 subjects were screened for eligibility, and 58 were randomized to sertraline (32) or placebo (26). Eight subjects from the sertraline arm and five from the placebo arm discontinued. Intent-to-treat analysis showed no significant difference from placebo on the primary outcomes (MSEL expressive language raw score and age equivalent combined score) or secondary outcomes. Sertraline was well tolerated, with no difference in side effects between sertraline and placebo groups. No serious adverse events possibly related to study treatment occurred. This randomized controlled trial of sertraline treatment showed no benefit with respect to primary or secondary outcome measures. For the 6-month period, treatment in young children with ASD appears safe, although the long-term side effects of low-dose sertraline in early childhood are unknown. www.ClinicalTrials.gov, identifier NCT02385799.
在观察性研究和轶事报告中显示,像舍曲林这样的选择性5-羟色胺再摄取抑制剂可改善脆性X综合征(FXS)幼儿的语言发育。先前一项针对FXS幼儿的舍曲林对照试验发现,在分析中,对于患有共病自闭症谱系障碍(ASD)的儿童,通过早期学习穆伦量表(MSEL)测量,其表达性语言发育有显著改善,这促使作者探究舍曲林在非综合征性ASD中是否也有疗效。作者在一项随机、双盲、安慰剂对照试验中,评估了低剂量舍曲林治疗6个月对58名年龄在24至72个月的ASD儿童的疗效。179名受试者接受了资格筛查,58名被随机分为舍曲林组(32名)或安慰剂组(26名)。舍曲林组有8名受试者、安慰剂组有5名受试者退出。意向性分析显示,在主要结局(MSEL表达性语言原始分数和年龄等效综合分数)或次要结局方面,与安慰剂相比无显著差异。舍曲林耐受性良好,舍曲林组和安慰剂组在副作用方面无差异。未发生可能与研究治疗相关的严重不良事件。这项舍曲林治疗的随机对照试验在主要或次要结局指标方面未显示出益处。在6个月期间,ASD幼儿的治疗似乎是安全的,尽管低剂量舍曲林在幼儿期的长期副作用尚不清楚。ClinicalTrials.gov网站,标识符NCT02385799。