Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorder

Florence Levy School of Psychiatry, University of New South Wales and Prince of Wales Hospital, Sydney, Australia Abstract: This review examines molecular genetic studies shown to be of importance in the etiology of attention-deficit/hyperactivity disorder (ADHD) and contrasts prefrontal versus sub...

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Main Author: Levy F
Format: Article
Language:English
Published: Dove Medical Press 2014-11-01
Series:Pharmacogenomics and Personalized Medicine
Online Access:http://www.dovepress.com/applications-of-pharmacogenetics-in-children-with-attention-deficithyp-peer-reviewed-article-PGPM
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author Levy F
author_facet Levy F
author_sort Levy F
collection DOAJ
description Florence Levy School of Psychiatry, University of New South Wales and Prince of Wales Hospital, Sydney, Australia Abstract: This review examines molecular genetic studies shown to be of importance in the etiology of attention-deficit/hyperactivity disorder (ADHD) and contrasts prefrontal versus subcortical mechanisms. Although these mechanisms are not completely dissociated, an understanding of prefrontal dopaminergic/noradrenergic versus subcortical D1/D2 receptor mechanisms is useful for studies of diagnosis versus potential adverse effects. Dopamine physiology, dopamine receptor studies, alpha-2 agonist studies, and dopamine transporter and potential new therapies are reviewed. Further understandings of molecular mechanisms involved in etiology versus treatment and adverse effects should help personalize the treatment of ADHD. Keywords: ADHD, dopamine transporter, dopamine receptors, alpha-2 agonists, COMT, stimulant side effects
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spelling doaj.art-e947b57a06d6422fab1cc33c47eaf6662022-12-22T00:51:45ZengDove Medical PressPharmacogenomics and Personalized Medicine1178-70662014-11-012014default34935619046Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorderLevy FFlorence Levy School of Psychiatry, University of New South Wales and Prince of Wales Hospital, Sydney, Australia Abstract: This review examines molecular genetic studies shown to be of importance in the etiology of attention-deficit/hyperactivity disorder (ADHD) and contrasts prefrontal versus subcortical mechanisms. Although these mechanisms are not completely dissociated, an understanding of prefrontal dopaminergic/noradrenergic versus subcortical D1/D2 receptor mechanisms is useful for studies of diagnosis versus potential adverse effects. Dopamine physiology, dopamine receptor studies, alpha-2 agonist studies, and dopamine transporter and potential new therapies are reviewed. Further understandings of molecular mechanisms involved in etiology versus treatment and adverse effects should help personalize the treatment of ADHD. Keywords: ADHD, dopamine transporter, dopamine receptors, alpha-2 agonists, COMT, stimulant side effectshttp://www.dovepress.com/applications-of-pharmacogenetics-in-children-with-attention-deficithyp-peer-reviewed-article-PGPM
spellingShingle Levy F
Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorder
Pharmacogenomics and Personalized Medicine
title Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorder
title_full Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorder
title_fullStr Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorder
title_full_unstemmed Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorder
title_short Applications of pharmacogenetics in children with attention-deficit/hyperactivity disorder
title_sort applications of pharmacogenetics in children with attention deficit hyperactivity disorder
url http://www.dovepress.com/applications-of-pharmacogenetics-in-children-with-attention-deficithyp-peer-reviewed-article-PGPM
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