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ERIC Number: EJ944789
Record Type: Journal
Publication Date: 2009-Dec
Pages: 10
Abstractor: As Provided
Reference Count: 0
ISSN: ISSN-0890-8567
A Candidate Gene Analysis of Methylphenidate Response in Attention-Deficit/Hyperactivity Disorder
McGough, James J.; McCracken, James T.; Loo, Sandra K.; Manganiello, Marc; Leung, Michael C.; Tietjens, Jeremy R.; Trinh, Thao; Baweja, Shilpa; Suddath, Robert; Smalley, Susan L.; Hellemann, Gerhard; Sugar, Catherine A.
Journal of the American Academy of Child & Adolescent Psychiatry, v48 n12 p1155-1164 Dec 2009
Objective: This study examines the potential role of candidate genes in moderating treatment effects of methylphenidate (MPH) in attention-deficit/hyperactivity disorder (ADHD). Method: Eighty-two subjects with ADHD aged 6 to 17 years participated in a prospective, double-blind, placebo-controlled, multiple-dose, crossover titration trial of immediate release MPH three times daily. The subjects were assessed on a variety of parent and clinician ratings and a laboratory math test. Data reduction based on principal components analysis identified statistically derived efficacy and side effect outcomes. Results: Attention-deficit/hyperactivity disorder symptom response was predicted by polymorphisms at the serotonin transporter ("SLC6A4") intron 2 VNTR (p = 0.01), with a suggested trend for catechol-O-methyltransferase ("COMT") (p = 0.04). Gene x dose interactions were noted on math test outcomes for the dopamine D4 receptor ("DRD4") promoter (p = 0.008), "DRD4" exon 3 "VNTR" (p = 0.006), and "SLC6A4" promoter insertion/deletion polymorphism ("5HTTLPR") (p = 0.02). Irritability was predicted by COMT (p = 0.02). Vegetative symptoms were predicted by "5HTTLPR" (p = 0.003). No significant effects were noted for the dopamine transporter ("SLC6A3") or synaptosomal-associated protein 25 ("SNAP25"). Conclusions: This article confirms and expands previous studies suggesting that genes moderate ADHD treatment response. The ADHD outcomes are not unitary but reflect both behavioral and learning domains that are likely influenced by different genes. Future research should emphasize candidate gene and genome-wide association studies in larger samples, symptom reduction as well as side effects outcomes, and responses over full therapeutic dose ranges to assess differences in both gene and gene x dose interactive effects. (Contains 4 tables and 2 figures.)
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Publication Type: Journal Articles; Reports - Research
Education Level: N/A
Audience: N/A
Language: English
Sponsor: N/A
Authoring Institution: N/A