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Received 2 July 2014; Accepted 26 July 2014Top of pageAbstractAnxiety disorders that are the most commonly occurring psychiatric disorders in childhood, are associated with a range of social and educational impairments and often continue into adulthood. Recent research suggests that some genetic variants may be associated with a more beneficial response to psychological therapy. Epigenetic mechanisms such as DNA methylation work at the interface between genetic and environmental influences. Furthermore, epigenetic alterations at the serotonin transporter (SERT) promoter region have been associated with environmental influences such as stressful life experiences. In this study, we measured DNA methylation upstream of SERT in 116 children with an anxiety disorder, before and after receiving CBT. Change during treatment in percentage DNA methylation was significantly different in treatment responders vs nonresponders. This effect was driven by one CpG site in particular, at which responders increased in methylation, whereas nonresponders showed a decrease in DNA methylation. This is the first study to demonstrate differences in SERT methylation change in association with response to a purely psychological therapy. These findings confirm that biological changes occur alongside changes in symptomatology following a psychological therapy such as CBT.Top of pageIntroductionAnxiety disorders have negative implications for many aspects of everyday functioning.1,2 They often arise during childhood and are not only associated with adult anxiety disorders but also with other forms of adult psychopathology such as depression.3,4 Cognitive behaviour therapy (CBT) is an effective treatment option for child and adolescent anxiety disorders with a remission rate of 56 following treatment, rising to around 65 at follow up.5,6 Research exploring predictors of response to CBT in childhood anxiety disorders is somewhat mixed, but provides modest support for factors such as pretreatment symptom severity, comorbidity and parental psychopathology.7, 8, 9, 10 These factors are consistent with a possible genetic basis to CBT response.Multiple genetic markers have been investigated for association with anxiety disorders and depression. Due to the success of anxiolytic and antidepressant drugs that target the serotonin transporter system11,12 and the critical role of the serotonin transporter in the termination of serotonergic neurotransmission, polymorphic variants of the serotonin transporter gene (SERT) have been widely studied. These findings reflect an interaction between genetic (5HTTLPR) and environmental (CBT) influences on outcome.Epigenetic mechanisms such as DNA methylation are thought to work at the interface between genes and the environment as they are sensitive to changes in environmental stimuli. The SERT promoter region has been shown to be particularly variable in DNA methylation across time,26 and differential DNA methylation patterns at this region have been associated with a range of negative life experiences. A study of SERT DNA methylation in adoptees found altered methylation patterns in those who experienced a range of negative life events and stressful situations such as child abuse and loss.27, 28, 29 In the case of unresolved loss or trauma, changes in DNA methylation associated with outcome were dependent on 5HTTLPR genotype. Monozygotic twins offer the opportunity to study the effects of environmental influences on SERT methylation while controlling for genetics. For example, in a study of monozygotic twins discordant for bullying victimization, increased SERT methylation patterns were identified in the bullied twins compared with their co twins with no history of bullying.30The investigation of DNA methylation and outcome following psychological therapy is a new area of research. One previous study of participants with borderline personality disorders (n suggested an association between poorer response to intensive dialectical behaviour therapy and increases in DNA methylation of the brain derived neurotrophic factor gene.31 Another study of veterans with posttraumatic stress disorder (n found that higher pretreatment glucocorticoid related NR3C1 methylation predicted treatment outcome, whereas FKBP5 gene methylation decreased across treatment time in association with recovery.32 However, some participants were also medicated in both studies.In this study, we compared SERT DNA methylation change from pre to post treatment in 116 children receiving CBT for an anxiety disorder. Specifically, we compared mean changes in methylation during the treatment period for those who had and had not remitted from their primary anxiety disorder by the end of treatment and by the follow up time point (6 months after the end of treatment). To our knowledge, this is the first study of response to a purely psychological therapy and changes in DNA methylation to focus on the SERT promoter region. Given the role played by DNA methylation in mediating the effect of the environment on emotional and behavioural outcomes, and previous findings that 5HTTLPR genotype is associated with treatment response, we hypothesized that treatment outcome would be associated with SERT DNA methylation changes during treatment.Top of pageMaterials and MethodsParticipantsSample Participants (n represent a subsample of a larger longitudinal study exploring genetic predictors of therapy response. Subjects were recruited at clinical sites in Sydney, Australia (n and Reading, UK (n and provided buccal swab DNA samples at assessment sessions pre and post treatment, within 2 weeks of the first and last treatment session, respectively. Participants ranged in age from 6 to 13 years (mean age years); 51.7 were male. All children completed a full course of manual based CBT for a primary diagnosis of an anxiety disorder. Details of the specific treatment protocols at each site have been reported elsewhere.25 All trials and collection of samples were approved by Human Ethics and Biosafety Committees at both clinical sites. Parents provided informed consent, children provided assent. The storage and analysis of DNA for this study were approved by the Psychiatry, Nursing and Midwifery Research Ethics Sub Committee at King College London, London, UK. Anxiety disorder diagnoses corresponded to a clinical severity rating of 4 or greater. Clinical diagnoses were made at assessment sessions pre and post treatment, and also at a follow up time point (6 months after the conclusion of treatment). Details of sample characteristics and primary anxiety disorder diagnoses made can be found in Table 1.Bisulphite PCR The SERT region targeted in this study is situated upstream of the promoter. To aid amplification, the sequence was split into two smaller, overlapping amplicons of 200 and 296 that covered the whole region (NCBI build 37, chromosome 17; (1) 28562753 (2) 28563022 see Supplementary Information, Figure 1a). Bisulphite PCR primers for each amplicon were designed using the Sequenom EpiDesigner software. PCR amplification was conducted using 45 cycles at an annealing temperature of 56 with Qiagen Hot Star Taq DNA Polymerase (Qiagen, UK) and Sequenom MassCLEAVE tagged primers (Primer sequences in Supplementary Information Table 1, amplicon sequences in Supplementary Information Figure 1b).Quality control Artificially fully methylated and unmethylated samples were included as assay controls. Following stringent quality control, quantitative methylation data from six CpG sites was obtained.Analyses We considered two measures of treatment response. First was primary anxiety response, defined as the absence of the primary anxiety diagnosis. Second was a broad anxiety response, defined as the absence of all anxiety diagnoses. Clinical outcome was assessed at posttreatment and at follow up (6 months after treatment). Average DNA methylation was calculated where data were available for at least five probes at both time points. Change in DNA methylation during treatment (from pre to posttreatment) was calculated for all CpG sites, and also as an average across the region. All analyses were performed in SPSS (version 20.0, IBM Corp, Armonk, NY, USA).To correct for multiple testing, a revised significance threshold was calculated using Matrix Spectral Decomposition.36 This method uses correlation between methylation levels at the CpG sites to give an effective number of independent variables to correct for. For primary and all anxiety diagnoses, remission rates were 48.3 and 29.3 at posttreatment, and 70.7 and 51.7 at follow up (Table 2). However, there were significant differences between responders and nonresponders. Treatment response groups (responders vs nonresponders for both primary anxiety outcome and all anxiety outcome, and improvers vs those who did not during the follow up period for primary anxiety outcome) did not differ on any demographic variables tested (Supplementary Table 3).Top of pageDiscussionOur findings suggest that treatment responders and nonresponders have differential patterns of methylation change across a course of CBT. Responders showed an increase in percentage DNA methylation during treatment at one CpG site in the SERT promoter region, whereas nonresponders decreased in percentage DNA methylation. 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