Garfunkel Danielle, Anagnostou Evdokia A, Aman Michael G, Handen Benjamin L, Sanders Kevin B, Macklin Eric A, Chan James, Veenstra-VanderWeele Jeremy
1Department of Psychiatry, Columbia University Medical Center, New York, New York.
2Bloorview Research Institute, Holland Bloorview Kids Rehabilitation Hospital, Toronto, Canada.
J Child Adolesc Psychopharmacol. 2019 Aug;29(6):448-455. doi: 10.1089/cap.2018.0171. Epub 2019 Jun 12.
We recently found that metformin attenuated weight gain due to mixed dopamine and serotonin receptor antagonists, commonly termed atypical antipsychotics, in children and adolescents with autism spectrum disorder (ASD). Previous studies have found that genetic variation predicts response to metformin in diabetes. In this study, we aimed to assess whether response to metformin for weight gain in this population is associated with variants in five genes previously implicated in metformin response in diabetes. Youth with ASD who experienced significant weight gain while taking mixed receptor antagonist medications were randomly assigned to metformin or placebo for 16 weeks, followed by open-label metformin treatment for 16 weeks. In the 53 participants with available DNA samples, we used a linear, mixed model analysis to assess response in the first 16 weeks of metformin treatment, whether in the randomized or open-label period, based upon genotypes at polymorphisms in five genes previously associated with metformin response in diabetes: , , , , and . In the primary analysis, both and showed significant effects of genotype on change in body mass index -scores, the primary outcome measure, during the first 16 weeks of treatment with metformin. No other polymorphism showed a significant difference. As has been shown for metformin treatment in diabetes, genetic variation may predict response to metformin for weight gain in youth with ASD treated with mixed receptor antagonists. Further work is needed to replicate these findings and evaluate whether they can be used prospectively to improve outcomes.
我们最近发现,在患有自闭症谱系障碍(ASD)的儿童和青少年中,二甲双胍可减轻因混合多巴胺和5-羟色胺受体拮抗剂(通常称为非典型抗精神病药物)导致的体重增加。先前的研究发现,基因变异可预测糖尿病患者对二甲双胍的反应。在本研究中,我们旨在评估该人群中二甲双胍对体重增加的反应是否与先前涉及糖尿病患者二甲双胍反应的五个基因的变异有关。在服用混合受体拮抗剂药物时体重显著增加的ASD青少年被随机分配接受二甲双胍或安慰剂治疗16周,随后接受为期16周的二甲双胍开放标签治疗。在53名有可用DNA样本的参与者中,我们使用线性混合模型分析,根据先前与糖尿病患者二甲双胍反应相关的五个基因多态性的基因型,评估二甲双胍治疗前16周(无论是随机期还是开放标签期)的反应。在初步分析中,在二甲双胍治疗的前16周,rs12208357和rs7903146均显示基因型对体重指数变化评分(主要结局指标)有显著影响。没有其他多态性显示出显著差异。正如在糖尿病患者二甲双胍治疗中所显示的那样,基因变异可能预测接受混合受体拮抗剂治疗的ASD青少年对二甲双胍体重增加的反应。需要进一步开展工作来重复这些发现,并评估它们是否可用于前瞻性地改善治疗结果。