Dopamine transporter gene and response to methylphenidate in attention-deficit/hyperactivity disorder

被引:97
作者
Roman, T
Szobot, C
Martins, D
Biederman, J
Rohde, LA
Hutz, MH
机构
[1] Univ Fed Rio Grande do Sul, Serv Psiquiatria Infancia & Adolescencia, Hosp Clin Porto Alegre, ADHD Outpatient Clin,Child & Adolescent Psychiat, BR-90035003 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Dept Genet, BR-90035003 Porto Alegre, RS, Brazil
[3] Harvard Univ, Sch Med, Pediat Psychopharmacol Unit, Massachusetts Gen Hosp, Boston, MA 02115 USA
来源
PHARMACOGENETICS | 2002年 / 12卷 / 06期
关键词
ADHD; methylphenidate; dopamine transporter gene;
D O I
10.1097/00008571-200208000-00011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study aims to evaluate whether a previously reported association between homozygosity for the 10-repeat allele of the dopamine transporter gene (10/10) and poor response to methylphenidate (MPH) would be replicated in a sample of Brazilian attention deficit/hyperactivity disorder (ADHD) boys. In a blind naturalistic study, 50 male ADHD youths were treated with MPH. Efficacy of the medication was measured by means of the 10-item Conners Abbreviated Rating Scale (ABRS), and the Children's Global Assessment Scale (CGAS). While 75% (15/20) of the youths without 10/10 genotype demonstrated an improvement higher than 50% in the ABRS scores with MPH, only 47% (14/30) of the subjects with 10/10 genotype achieved the same level of improvement with medication (one-tailed P=0.04). In addition, the group without this genotype had significantly higher increase in the CGAS scores than the other group (one-tailed P < 0.01). Our findings support an association between homozygosity for the 10-repeat allele at dopamine transporter gene locus and poor response to MPH.
引用
收藏
页码:497 / 499
页数:3
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