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可能涉及 NET1 的遗传变异在注意缺陷多动障碍共患对立违抗性障碍的发病机制中的作用。

The possible involvement of genetic variants of NET1 in the etiology of attention-deficit/hyperactivity disorder comorbid with oppositional defiant disorder.

机构信息

Peking University Sixth Hospital, Institute of Mental Health, Beijing, China; Key Laboratory of Mental Health, Ministry of Health (Peking University), Beijing, China.

出版信息

J Child Psychol Psychiatry. 2015 Jan;56(1):58-66. doi: 10.1111/jcpp.12278. Epub 2014 Jun 19.

Abstract

BACKGROUND

Attention-deficit/hyperactivity disorder (ADHD) and oppositional defiant disorder (ODD) often coexist and shared some genetic influences. Evidence from the existing literature indicated that comorbid with ODD may increase the heterogeneity of ADHD genetics. Our present study sought to investigate the role of norepinephrine transporter gene (NET1) for ADHD comorbid with ODD.

METHODS

Six single nucleotide polymorphisms (SNPs) of NET1 were genotyped for a total of 1,815 ADHD cases, including 587 subjects (32.3%) with ODD. Chi-square tests were conducted for pseudo case-control study comparing allelic and genotypic distributions between ADHD with and without ODD. Among them, there were 1,249 probands together with their parents composing trios for family-based association studies using transmission disequilibrium tests (TDTs). In addition, 1,337 ADHD probands have detailed information of ODD symptoms and were included for quantitative analyses with genotypes using analyses of covariance (ANCOVA). To consider the overlap and correlation of other comorbidities with ODD and eliminate their potential confounding effect, we further repeated above analyses for 'pure ADHD+ODD' versus 'ADHD-only' after excluding other comorbidities except for ODD.

RESULTS

The pseudo case-control study showed different allelic and genotypic distributions of SNP rs3785143 between ADHD with ODD and those without ODD. Family-based association tests indicated overtransmission of the T allele of rs3785143 in ADHD with ODD trios, but no biased transmission in those without ODD. ANCOVA showed association between genotypes of rs3785143 with ODD symptoms in ADHD probands, especially with 'Argumentative/Defiant Behavior (ADB)' dimension after controlling gender, age, clinical subtypes and intelligence. Above association still existed after removing the samples with other comorbidities.

CONCLUSION

NET1 was associated with comorbidity of ODD and ODD symptoms in ADHD probands. Our findings emphasize the importance of considering the comorbidity of ODD in ADHD genetic studies, especially ADHD with ADB. However, further replication in independent sample or different populations is still needed.

摘要

背景

注意力缺陷多动障碍(ADHD)和对立违抗性障碍(ODD)经常共存,并有一些共同的遗传影响。现有文献证据表明,与 ODD 共病可能会增加 ADHD 遗传的异质性。本研究旨在探讨去甲肾上腺素转运体基因(NET1)在 ADHD 合并 ODD 中的作用。

方法

对 1815 例 ADHD 病例(包括 587 例(32.3%)伴 ODD)进行 NET1 的 6 个单核苷酸多态性(SNP)基因分型。采用卡方检验比较 ADHD 伴或不伴 ODD 的等位基因和基因型分布。其中,1249 名先证者及其父母组成三体型,用于采用传递不平衡检验(TDT)的家系关联研究。此外,1337 名 ADHD 先证者有详细的 ODD 症状信息,并用基因型进行方差分析(ANCOVA)进行定量分析。为了考虑与 ODD 共病的其他疾病的重叠和相关性,并消除其潜在的混杂效应,我们在排除除 ODD 以外的其他共病后,对“单纯 ADHD+ODD”与“单纯 ADHD”进行了上述分析。

结果

假性病例对照研究显示,ADHD 伴 ODD 与不伴 ODD 的 SNP rs3785143 存在不同的等位基因和基因型分布。家系关联检验显示,在 ADHD 伴 ODD 三体型中,rs3785143 的 T 等位基因传递过度,但在不伴 ODD 的三体型中无偏传递。ANCOVA 显示,在 ADHD 先证者中,rs3785143 的基因型与 ODD 症状之间存在关联,尤其是在控制性别、年龄、临床亚型和智力后与“争辩/挑衅行为(ADB)”维度存在关联。在去除伴有其他共病的样本后,上述关联仍然存在。

结论

NET1 与 ADHD 先证者 ODD 共病和 ODD 症状相关。我们的研究结果强调了在 ADHD 遗传研究中考虑 ODD 共病的重要性,尤其是 ADHD 伴 ADB。然而,仍需要在独立样本或不同人群中进行进一步验证。

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