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作 者:李君[1] 王玉凤[1] 周儒伦[1] 张浩波[1] 汪冰[1] 杨莉[1]
出 处:《北京大学学报(医学版)》2006年第5期492-495,共4页Journal of Peking University:Health Sciences
基 金:卫生部临床学科重点项目(2004-468);北京市科技计划项目(Y0204003040831);科技部攻关项目(2004BA720A20)基金资助~~
摘 要:目的:探讨共患和不共患破坏性行为障碍(DBD)的儿童注意缺陷多动障碍(ADHD)与5-HT1D受体基因(HTR1D)1350T>C和1236A>G两种多态之间的关联。方法:检测90个共患DBD的ADHD核心家系和182个不共患DBD的ADHD核心家系的1350T>C和1236A>G两种多态,并分别进行传递不平衡(TDT)检验和单体型分析。结果:在共患DBD的家系中,1350T等位基因(χ2=3.67,P=0.055)和G/T单体型(χ2=3.84,P=0.050)优先传递,1350C等位基因(χ2=3.67,P=0.055)和G/C单体型(χ2=5.22,P=0.022)传递减少。在不共患DBD的家系中未发现任何等位基因和单体型的传递不平衡现象。结论:ADHD共患DBD与否在HTR1D受体基因多态水平存在遗传差别,遗传在共患DBD的ADHD中具有更重要的作用。Objective: To investigate the relationship between two HTR1 D gene polymorphisms, that is 1350T 〉 C and 1236A 〉 G polymorphisms, and attention deficit hyperactivity disorder (ADHD) comorbid or not comorbid disruptive behavior disorder (DBD). Methods: Blood samples were taken from 90 trios with probands of ADHD comrbid DBD and 182 trios with probands of ADHD not comorbid DBD. DNA was extracted. 1350T 〉 C and 1236A 〉 G were genotyped by restriction fragment length polymorphism analysis. Transmit/disequilibrium test and haplotype analysis were used to test the association of the two polymorphisms of HTR1 D gene and ADHD comorbid or not comorbid disruptive behavior disorder (DBD) separately. Results : 1350T allele (χ^2 = 3.67, P = 0. 055 ) and G/T haplotype ( χ^2 = 3.84, P = 0. 050 ) were overtransmitted, while 1350C allele (χ^2 = 3.67, P = 0. 055 ) and G/C haplotype (χ^2 = 5.22, P = 0. 022) were undertransmitted to probands of ADHD with DBD. No biased transmission of any allele and haplotype was found in families with probands of ADHD without DBD. Conclusion: ADHD comorbid or not comorbid DBD are different at the level of HTR1D gene polymrohisms of 1350T 〉 C and 1236A 〉 G. The current results indicate that ADHD with DBD has more heritable backgrounds when compared with ADHD without DBD.
关 键 词:注意缺陷和分裂性行为障碍 受体 血清素 基因 连锁不平衡 单元型
分 类 号:R742.89[医药卫生—神经病学与精神病学]
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