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微管相关蛋白1B(MAP1B)基因和一氧化氮合酶1(NOS1)基因与患有注意力缺陷多动障碍的青少年的工作记忆有关。

MAP1B and NOS1 genes are associated with working memory in youths with attention-deficit/hyperactivity disorder.

作者信息

Salatino-Oliveira Angélica, Wagner Flávia, Akutagava-Martins Glaucia C, Bruxel Estela M, Genro Júlia P, Zeni Cristian, Kieling Christian, Polanczyk Guilherme V, Rohde Luis A, Hutz Mara H

机构信息

Department of Genetics, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Division of Child and Adolescent Psychiatry, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2016 Jun;266(4):359-66. doi: 10.1007/s00406-015-0626-9. Epub 2015 Aug 2.

Abstract

Diverse efforts have been done to improve the etiologic understanding of mental disorders, such as attention-deficit/hyperactivity disorder (ADHD). It becomes clear that research in mental disorders needs to move beyond descriptive syndromes. Several studies support recent theoretical models implicating working memory (WM) deficits in ADHD complex neuropsychology. The aim of this study was to examine the association between rs2199161 and rs478597 polymorphisms at MAP1B and NOS1 genes with verbal working memory in children and adolescents with ADHD. A total of 253 unrelated ADHD children/adolescents were included. The sample was diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders-4th edition criteria. Digit Span from the Wechsler Intelligence Scale for Children-Third Edition was used to assess verbal WM. The raw scores from both forward and backward conditions of Digit Span were summed and converted into scaled scores according to age. The means of scaled Digit Span were compared according to genotypes by ANOVA. Significant differences in Digit Span scores between MAP1B genotype groups (rs2199161: F = 5.676; p = 0.018) and NOS1 (rs478597: F = 6.833; p = 0.009) genes were detected. For both polymorphisms, the CC genotype carriers showed a worse performance in WM task. Our findings suggest possible roles of NOS1 and MAP1B genes in WM performance in ADHD patients, replicating previous results with NOS1 gene in this cognitive domain in ADHD children.

摘要

人们已经做出了各种努力来增进对精神障碍(如注意力缺陷多动障碍,ADHD)病因的理解。很明显,精神障碍的研究需要超越描述性综合征。多项研究支持了近期的理论模型,这些模型认为工作记忆(WM)缺陷与ADHD复杂的神经心理学有关。本研究的目的是检验MAP1B和NOS1基因的rs2199161和rs478597多态性与ADHD儿童和青少年言语工作记忆之间的关联。总共纳入了253名无亲属关系的ADHD儿童/青少年。样本根据《精神障碍诊断与统计手册》第4版标准进行诊断。使用韦氏儿童智力量表第三版中的数字广度来评估言语工作记忆。将数字广度正向和反向条件下的原始分数相加,并根据年龄转换为量表分数。通过方差分析根据基因型比较数字广度量表分数的均值。在MAP1B基因型组(rs2199161:F = 5.676;p = 0.018)和NOS1(rs478597:F = 6.833;p = 0.009)基因之间检测到数字广度分数存在显著差异。对于这两种多态性,CC基因型携带者在工作记忆任务中的表现较差。我们的研究结果表明NOS1和MAP1B基因在ADHD患者的工作记忆表现中可能发挥作用,这与之前在ADHD儿童这一认知领域中关于NOS1基因的研究结果一致。

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