Transcription Factor Activating Protein-2β (TFAP-2β) genotype and symptoms of attention deficit hyperactivity disorder in relation to symptoms of depression in two independent samples

被引:5
作者
Nilsson, Kent W. [1 ]
Sonnby, Karin [1 ]
Nordquist, Niklas [2 ]
Comasco, Erika [2 ]
Leppert, Jerzy [1 ]
Oreland, Lars [2 ]
Sjoberg, Rickard L. [3 ]
机构
[1] Uppsala Univ, Vastmanland Cty Hosp, Clin Res Ctr, S-72189 Vasteras, Sweden
[2] Uppsala Univ, Dept Neurosci, S-75124 Uppsala, Sweden
[3] Univ Hosp Umea, Dept Neurosurg, S-90185 Umea, Sweden
基金
瑞典研究理事会;
关键词
ADHD; Adolescents; Comorbidity; Depression; Gene-environment interaction; Transcription factor AP-2 beta; SEROTONIN TRANSPORTER GENE; MAO-A GENE; TRANSCRIPTION FACTOR; MAJOR DEPRESSION; FAMILY FUNCTION; ADULT ADHD; ADOLESCENT; GENDER; SEX; ASSOCIATION;
D O I
10.1007/s00787-013-0450-6
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
The Transcription Factor Activating Protein-2 beta (TFAP-2 beta) gene has been shown to influence monoaminergic neurotransmission, and several genes important for monoaminergic function have binding sites for TFAP-2 beta. Familial studies of attention deficit hyperactivity disorder (ADHD) suggest a hereditary-determined subtype of ADHD with comorbid depression. We examined a functional variation of the TFAP-2 beta gene in the context of co-occurring symptoms of ADHD and depression in two independent population-based samples of adolescents (Group A, n = 175 and Group B, n = 1,506) from Sweden. Results indicated 6.1 to 7.8 % of adolescents screened positively for ADHD and depression symptoms. Symptoms of depression were more common among girls who screened positively for ADHD and did not carry the nine-repeat allele of the TFAP-2 beta intron 1 Variable Number Tandem Repeat (VNTR) polymorphism. The presence of the nine-repeat variant of the TFAP-2 beta intron 1 VNTR appears to protect girls with ADHD symptoms from the co-expression of symptoms of depression.
引用
收藏
页码:207 / 217
页数:11
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