1. Genome-wide association study of response to cognitive-behavioural therapy in children with anxiety disorders
- Author
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Coleman, Jonathan R I, Lester, Kathryn J, Keers, Robert, Roberts, Susanna, Curtis, Charles, Arendt, Kristian, Bögels, Susan, Cooper, Peter, Creswell, Cathy, Dalgleish, Tim, Hartman, Catharina A, Heiervang, Einar R, Hötzel, Katrin, Hudson, Jennifer L, In-Albon, Tina, Lavallee, Kristen, Lyneham, Heidi J, Marin, Carla E, Meiser-Stedman, Richard, Morris, Talia, Nauta, Maaike H, Rapee, Ronald M, Schneider, Silvia, Schneider, Sophie C, Silverman, Wendy K, Thastum, Mikael, Thirlwall, Kerstin, Waite, Polly, Wergeland, Gro Janne, Breen, Gerome, Eley, Thalia C, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Clinical Psychology and Experimental Psychopathology, and Developmental Psychopathology (RICDE, FMG)
- Subjects
Male ,Adolescent ,Cognitive Behavioral Therapy ,Genotype ,VARIANTS ,DEPRESSION ,GENE ,Anxiety Disorders ,Polymorphism, Single Nucleotide ,PANIC DISORDER ,Treatment Outcome ,Child, Preschool ,REPLICATION ,Papers ,LINKAGE ,ANTIDEPRESSANT RESPONSE ,Humans ,Female ,PREDICTORS ,Child ,METAANALYSIS ,POPULATION ,Genome-Wide Association Study - Abstract
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
- Published
- 2015
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