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中国儿童和青少年注意缺陷多动障碍 COMT 基因 Val158Met 多态性与儿茶酚胺能神经递质血清浓度。

Val158Met polymorphisms of COMT gene and serum concentrations of catecholaminergic neurotransmitters of ADHD in Chinese children and adolescents.

机构信息

Department of Child Health, Maternal and Child Health Hospital of Hubei Province, Wuhan, China.

Department of Maternal and Child Health, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.

出版信息

Medicine (Baltimore). 2021 Dec 10;100(49):e27867. doi: 10.1097/MD.0000000000027867.

Abstract

This study analyzed the Val158Met polymorphisms of the catechol-O-methyltransferase (COMT) gene and serum concentrations of catecholaminergic neurotransmitters in attention deficit hyperactivity disorder (ADHD) children and adolescents.All the subjects (180 paired ADHD and non-ADHD children and adolescents) were genotyped for the Val158Met polymorphisms of the COMT gene, and determined by the difference of dopamine and noradrenalin from a 1:1 paired case-control study.The frequencies of methionine (A)/A, valine (G)/A, and G/G were 51.67%, 41.11%, and 7.22% in the case group, and 62.22%, 31.11%, and 6.67% in the control group. There was a significant difference in the distribution of all genotypes of the COMT gene between the 2 groups (odds ratio = 1.85, 95% confidence interval: 1.62-2.08; χ2 = 7.80, P < .05). The serum concentrations of dopamine and noradrenalin were 1.42 ± 0.34 ng/mL and 177.70 ± 37.92 pg/mL in the case group, and 1.94 ± 0.42 ng/mL and 206.20 ± 42.45 pg/mL in the control group. There were the significant differences in the levels of dopamine and noradrenalin between the 2 groups (dopamine: t = 4.30, P < .01; noradrenalin: t = 2.24, P < .05).Our study suggested that the Val158Met polymorphisms of the COMT gene and serum concentrations of catecholaminergic neurotransmitters were associated with ADHD children and adolescents.

摘要

这项研究分析了儿茶酚-O-甲基转移酶(COMT)基因的 Val158Met 多态性和注意缺陷多动障碍(ADHD)儿童和青少年的儿茶酚胺能神经递质的血清浓度。所有受试者(180 对 ADHD 和非 ADHD 儿童和青少年)均进行 COMT 基因 Val158Met 多态性基因分型,并通过 1:1 配对病例对照研究中多巴胺和去甲肾上腺素的差异来确定。病例组中 Met/A、Val/G 和 G/G 的频率分别为 51.67%、41.11%和 7.22%,对照组分别为 62.22%、31.11%和 6.67%。两组间 COMT 基因所有基因型的分布存在显著差异(比值比 = 1.85,95%置信区间:1.62-2.08;χ2 = 7.80,P < .05)。病例组中多巴胺和去甲肾上腺素的血清浓度分别为 1.42±0.34ng/mL 和 177.70±37.92pg/mL,对照组分别为 1.94±0.42ng/mL 和 206.20±42.45pg/mL。两组间多巴胺和去甲肾上腺素水平存在显著差异(多巴胺:t = 4.30,P < .01;去甲肾上腺素:t = 2.24,P < .05)。我们的研究表明,COMT 基因的 Val158Met 多态性和儿茶酚胺能神经递质的血清浓度与 ADHD 儿童和青少年有关。

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Attention-Deficit/Hyperactivity Disorder.注意力缺陷多动障碍
Adv Pediatr. 2016 Aug;63(1):255-80. doi: 10.1016/j.yapd.2016.04.017.

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