Atomoxetine improved attention in children and adolescents with attention-deficit/hyperactivity disorder and dyslexia in a 16 week, acute, randomized, double-blind trial

dc.contributor.authorWietecha, Linda
dc.contributor.authorWilliams, David
dc.contributor.authorShaywitz, Sally
dc.contributor.authorShaywitz, Bennett
dc.contributor.authorHooper, Stephen R.
dc.contributor.authorWigal, Sharon B.
dc.contributor.authorDunn, David
dc.contributor.authorMcBurnett, Keith
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2015-09-15T15:18:41Z
dc.date.available2015-09-15T15:18:41Z
dc.date.issued2013-11
dc.description.abstractOBJECTIVE: The purpose of this study was to evaluate atomoxetine treatment effects in attention-deficit/hyperactivity disorder (ADHD-only), attention-deficit/hyperactivity disorder with comorbid dyslexia (ADHD+D), or dyslexia only on ADHD core symptoms and on sluggish cognitive tempo (SCT), working memory, life performance, and self-concept. METHODS: Children and adolescents (10-16 years of age) with ADHD+D (n=124), dyslexia-only (n=58), or ADHD-only (n=27) received atomoxetine (1.0-1.4 mg/kg/day) or placebo (ADHD-only subjects received atomoxetine) in a 16 week, acute, randomized, double-blind trial with a 16 week, open-label extension phase (atomoxetine treatment only). Changes from baseline were assessed to weeks 16 and 32 in ADHD Rating Scale-IV-Parent-Version:Investigator-Administered and Scored (ADHDRS-IV-Parent:Inv); ADHD Rating Scale-IV-Teacher-Version (ADHDRS-IV-Teacher-Version); Life Participation Scale-Child- or Parent-Rated Version (LPS); Kiddie-Sluggish Cognitive Tempo (K-SCT) Interview; Multidimensional Self Concept Scale (MSCS); and Working Memory Test Battery for Children (WMTB-C). RESULTS: At week 16, atomoxetine treatment resulted in significant (p<0.05) improvement from baseline in subjects with ADHD+D versus placebo on ADHDRS-IV-Parent:Inv Total (primary outcome) and subscales, ADHDRS-IV-Teacher-Version Inattentive subscale, K-SCT Interview Parent and Teacher subscales, and WMTB-C Central Executive component scores; in subjects with Dyslexia-only, atomoxetine versus placebo significantly improved K-SCT Youth subscale scores from baseline. At Week 32, atomoxetine-treated ADHD+D subjects significantly improved from baseline on all measures except MSCS Family subscale and WMTB-C Central Executive and Visuo-spatial Sketchpad component scores. The atomoxetine-treated dyslexia-only subjects significantly improved from baseline to week 32 on ADHDRS-IV-Parent:Inv Inattentive subscale, K-SCT Parent and Teacher subscales, and WMTB-C Phonological Loop and Central Executive component scores. The atomoxetine-treated ADHD-only subjects significantly improved from baseline to Week 32 on ADHDRS-Parent:Inv Total and subscales, ADHDRS-IV-Teacher-Version Hyperactive/Impulsive subscale, LPS Self-Control and Total, all K-SCT subscales, and MSCS Academic and Competence subscale scores. CONCLUSIONS: Atomoxetine treatment improved ADHD symptoms in subjects with ADHD+D and ADHD-only, but not in subjects with dyslexia-only without ADHD. This is the first study to report significant effects of any medication on SCT.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationWietecha, L., Williams, D., Shaywitz, S., Shaywitz, B., Hooper, S. R., Wigal, S. B., … McBurnett, K. (2013). Atomoxetine Improved Attention in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder and Dyslexia in a 16 Week, Acute, Randomized, Double-Blind Trial. Journal of Child and Adolescent Psychopharmacology, 23(9), 605–613. http://doi.org/10.1089/cap.2013.0054en_US
dc.identifier.urihttps://hdl.handle.net/1805/6912
dc.language.isoen_USen_US
dc.publisherMary Ann Lieberten_US
dc.relation.isversionof10.1089/cap.2013.0054en_US
dc.relation.journalJournal of Child and Adolescent Psychopharmacologyen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectAdolescenten_US
dc.subjectAdrenergic Uptake Inhibitors -- administration & dosageen_US
dc.subjectAdrenergic Uptake Inhibitors -- therapeutic useen_US
dc.subjectAttention Deficit Disorder with Hyperactivity -- drug therapyen_US
dc.subjectAttention Deficit Disorder with Hyperactivity -- physiopathologyen_US
dc.subjectChilden_US
dc.subjectCognition -- drug effectsen_US
dc.subjectDouble-Blind Methoden_US
dc.subjectDyslexia -- drug therapyen_US
dc.subjectDyslexia -- physiopathologyen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectMemory, Short-Term -- drug effectsen_US
dc.subjectPropylamines -- administration & dosageen_US
dc.subjectPropylamines -- therapeutic useen_US
dc.subjectPsychiatric Status Rating Scalesen_US
dc.subjectSelf Concepten_US
dc.subjectSeverity of Illness Indexen_US
dc.subjectTime Factorsen_US
dc.subjectTreatment Outcomeen_US
dc.titleAtomoxetine improved attention in children and adolescents with attention-deficit/hyperactivity disorder and dyslexia in a 16 week, acute, randomized, double-blind trialen_US
dc.typeArticleen_US
ul.alternative.fulltexthttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842866/en_US
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