Lester Kathryn J, Coleman Jonathan R I, Roberts Susanna, Keers Robert, Breen Gerome, Bögels Susan, Creswell Cathy, Hudson Jennifer L, McKinnon Anna, Nauta Maaike, Rapee Ronald M, Schneider Silvia, Silverman Wendy K, Thastum Mikael, Waite Polly, Wergeland Gro Janne H, Eley Thalia C
School of Psychology, University of Sussex, Brighton, UK.
King's College London, MRC Social, Genetic and Developmental Psychiatry (SGDP) Centre, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Am J Med Genet B Neuropsychiatr Genet. 2017 Mar;174(2):144-155. doi: 10.1002/ajmg.b.32467. Epub 2016 Jun 27.
Extinction learning is an important mechanism in the successful psychological treatment of anxiety. Individual differences in response and relapse following Cognitive Behavior Therapy may in part be explained by variability in the ease with which fears are extinguished or the vulnerability of these fears to re-emerge. Given the role of the endocannabinoid system in fear extinction, this study investigates whether genetic variation in the endocannabinoid system explains individual differences in response to CBT. Children (N = 1,309) with a primary anxiety disorder diagnosis were recruited. We investigated the relationship between variation in the CNR1, CNR2, and FAAH genes and change in primary anxiety disorder severity between pre- and post-treatment and during the follow-up period in the full sample and a subset with fear-based anxiety disorder diagnoses. Change in symptom severity during active treatment was nominally associated (P < 0.05) with two SNPs. During the follow-up period, five SNPs were nominally associated with a poorer treatment response (rs806365 [CNR1]; rs2501431 [CNR2]; rs2070956 [CNR2]; rs7769940 [CNR1]; rs2209172 [FAAH]) and one with a more favorable response (rs6928813 [CNR1]). Within the fear-based subset, the effect of rs806365 survived multiple testing corrections (P < 0.0016). We found very limited evidence for an association between variants in endocannabinoid system genes and treatment response once multiple testing corrections were applied. Larger, more homogenous cohorts are needed to allow the identification of variants of small but statistically significant effect and to estimate effect sizes for these variants with greater precision in order to determine their potential clinical utility. © 2016 The Authors. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Published by Wiley Periodicals, Inc.
消退学习是焦虑症成功心理治疗的重要机制。认知行为疗法后反应和复发的个体差异,部分可能由恐惧消退的难易程度或这些恐惧重新出现的易感性差异来解释。鉴于内源性大麻素系统在恐惧消退中的作用,本研究调查内源性大麻素系统的基因变异是否能解释个体对认知行为疗法反应的差异。招募了被诊断患有原发性焦虑症的儿童(N = 1309)。我们在全样本以及患有基于恐惧的焦虑症诊断的子集中,研究了CNR1、CNR2和FAAH基因变异与治疗前和治疗后以及随访期间原发性焦虑症严重程度变化之间的关系。积极治疗期间症状严重程度的变化与两个单核苷酸多态性(SNP)名义上相关(P < 0.05)。在随访期间,五个SNP名义上与较差的治疗反应相关(rs806365 [CNR1];rs2501431 [CNR2];rs2070956 [CNR2];rs7769940 [CNR1];rs2209172 [FAAH]),一个与更有利的反应相关(rs6928813 [CNR1])。在基于恐惧的子集中,rs806365的效应在多重检验校正后仍然显著(P < 0.0016)。一旦应用多重检验校正,我们发现内源性大麻素系统基因变异与治疗反应之间关联的证据非常有限。需要更大、更同质的队列,以便识别具有小但统计学显著效应的变异,并更精确地估计这些变异的效应大小,从而确定它们的潜在临床效用。© 2016作者。《美国医学遗传学杂志B辑:神经精神遗传学》由威利期刊公司出版