儿童注意力缺陷/多动障碍的常见肥胖风险等位基因。

Özgür Albayrak, Carolin Pütter, Anna-Lena Volckmar, Sven Cichon, Per Hoffmann, Markus M Nöthen, Karl-Heinz Jöckel, Stefan Schreiber, H-Erich Wichmann, Stephen V Faraone, Benjamin M Neale, Beate Herpertz-Dahlmann, Gerd Lehmkuhl, Judith Sinzig, Tobias J Renner, Marcel Romanos, Andreas Warnke, Klaus-Peter Lesch, Andreas Reif, Benno G Schimmelmann, André Scherag, Johannes Hebebrand, Anke Hinney
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引用次数: 79

摘要

患有注意力缺陷/多动障碍(ADHD)的儿童比没有多动症的儿童有更高的肥胖率。肥胖风险等位基因可能与多动症相关的等位基因重叠。我们研究了体重指数(BMI)增加的风险等位基因是否与多动症和相关的数量特征(注意力不集中和多动/冲动)相关。我们在一项ADHD全基因组关联研究(GWAS)中筛选了32个单核苷酸多态性(snp)肥胖风险等位基因,该研究基于495名患者和1300名基于人群的对照,并在一项ADHD荟萃分析中对这些snp进行了计算机分析,该荟萃分析包括2064个三人组、896个独立病例和2455名对照。在德国样本中,NUDT3基因中的rs206936 (nudix;核苷二磷酸连接片段x型基序3)与ADHD风险相关(OR: 1.39;P = 3.4 × 10(-4);Pcorr = 0.01)。在meta分析数据中,我们发现rs6497416位于GPRC5B基因(G蛋白偶联受体,C家族,5组,成员B;P = 7.2 × 10(-4);Pcorr = 0.02)为ADHD的风险等位基因。GPRC5B属于代谢性谷氨酸受体家族,该家族与ADHD的病因有关。在德国样本中,葡萄糖胺-6-磷酸脱氨酶2基因(GNPDA2)中的rs206936 (NUDT3)和rs10938397与注意力不集中相关,而丝裂原活化蛋白激酶5基因(MAP2K5)和细胞粘附分子2基因(CADM2)中的标记与多动症相关。在meta分析数据中,MAP2K5与注意力不集中相关,GPRC5B与多动/冲动性和注意力不集中相关,CADM2与多动/冲动性相关。我们的研究结果为进一步研究ADHD和肥胖的共同遗传背景提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder.

Children with attention-deficit/hyperactivity disorder (ADHD) have a higher rate of obesity than children without ADHD. Obesity risk alleles may overlap with those relevant for ADHD. We examined whether risk alleles for an increased body mass index (BMI) are associated with ADHD and related quantitative traits (inattention and hyperactivity/impulsivity). We screened 32 obesity risk alleles of single nucleotide polymorphisms (SNPs) in a genome-wide association study (GWAS) for ADHD based on 495 patients and 1,300 population-based controls and performed in silico analyses of the SNPs in an ADHD meta-analysis comprising 2,064 trios, 896 independent cases, and 2,455 controls. In the German sample rs206936 in the NUDT3 gene (nudix; nucleoside diphosphate linked moiety X-type motif 3) was associated with ADHD risk (OR: 1.39; P = 3.4 × 10(-4) ; Pcorr  = 0.01). In the meta-analysis data we found rs6497416 in the intronic region of the GPRC5B gene (G protein-coupled receptor, family C, group 5, member B; P = 7.2 × 10(-4) ; Pcorr  = 0.02) as a risk allele for ADHD. GPRC5B belongs to the metabotropic glutamate receptor family, which has been implicated in the etiology of ADHD. In the German sample rs206936 (NUDT3) and rs10938397 in the glucosamine-6-phosphate deaminase 2 gene (GNPDA2) were associated with inattention, whereas markers in the mitogen-activated protein kinase 5 gene (MAP2K5) and in the cell adhesion molecule 2 gene (CADM2) were associated with hyperactivity. In the meta-analysis data, MAP2K5 was associated with inattention, GPRC5B with hyperactivity/impulsivity and inattention and CADM2 with hyperactivity/impulsivity. Our results justify further research on the elucidation of the common genetic background of ADHD and obesity.

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