...
首页> 外文期刊>International Journal of Energy, Information and Communications >Genome-wide association study of response to cognitive–behavioural therapy in children with anxiety disorders
【24h】

Genome-wide association study of response to cognitive–behavioural therapy in children with anxiety disorders

机译:全基因组关联研究对焦虑症患儿认知行为治疗的反应

获取原文
           

摘要

Background Anxiety disorders are common, and cognitive–behavioural therapy (CBT) is a first-line treatment. Candidate gene studies have suggested a genetic basis to treatment response, but findings have been inconsistent. Aims To perform the first genome-wide association study (GWAS) of psychological treatment response in children with anxiety disorders ( n = 980). Method Presence and severity of anxiety was assessed using semi-structured interview at baseline, on completion of treatment (post-treatment), and 3 to 12 months after treatment completion (follow-up). DNA was genotyped using the Illumina Human Core Exome-12v1.0 array. Linear mixed models were used to test associations between genetic variants and response (change in symptom severity) immediately post-treatment and at 6-month follow-up. Results No variants passed a genome-wide significance threshold ( P = 5 × 10?8) in either analysis. Four variants met criteria for suggestive significance ( P 5 × 10?6) in association with response post-treatment, and three variants in the 6-month follow-up analysis. Conclusions This is the first genome-wide therapygenetic study. It suggests no common variants of very high effect underlie response to CBT. Future investigations should maximise power to detect single-variant and polygenic effects by using larger, more homogeneous cohorts.
机译:背景焦虑症很常见,认知行为疗法(CBT)是一线治疗。候选基因研究表明了治疗反应的遗传基础,但发现并不一致。目的对焦虑症患儿(n = 980)进行心理治疗反应的第一个全基因组关联研究(GWAS)。方法在基线,治疗完成时(治疗后)和治疗完成后3至12个月(随访),使用半结构式访谈评估焦虑的存在和严重程度。使用Illumina Human Core Exome-12v1.0阵列对DNA进行基因分型。线性混合模型用于在治疗后和6个月的随访中测试遗传变异与反应(症状严重性变化)之间的关联。结果在任一分析中,没有变异体通过全基因组显着性阈值(P = 5×10?8)。四个变体与治疗后反应相关,符合提示显着性标准(P <5×10?6),六个月的随访分析中三个变体。结论这是第一个全基因组治疗遗传学研究。这表明对CBT的响应没有任何非常有效的常见变异。未来的研究应该通过使用更大,更同质的队列来最大程度地检测单变量和多基因效应。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号