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与尼古丁依赖相关的 CHRNA5-CHRNA3-CHRNB4 簇中的风险基因变异与认知表现相关。

Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance.

机构信息

Cologne Center for Genomics, University of Cologne, Cologne, Germany.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1448-58. doi: 10.1002/ajmg.b.31126. Epub 2010 Sep 30.


DOI:10.1002/ajmg.b.31126
PMID:20886544
Abstract

Recent studies strongly support an association of the nicotinic acetylcholine receptor gene cluster CHRNA5-CHRNA3-CHRNB4 with nicotine dependence (ND). However, the precise genotype-phenotype relationship is still unknown. Clinical and epidemiological data on smoking behavior raise the possibility that the relevant gene variants may indirectly contribute to the development of ND by affecting cognitive performance in some smokers who consume nicotine for reasons of "cognition enhancement." Here, we tested seven single nucleotide polymorphisms (SNPs) rs684513, rs637137, rs16969968, rs578776, rs1051730, rs3743078, rs3813567 from the CHRNA5-CHRNA3-CHRNB4 gene cluster for association with ND, measures of cognitive performance and gene expression. As expected, we found all SNPs being associated with ND in three independent cohorts (KORA, NCOOP, ESTHER) comprising 5,561 individuals. In an overlapping sample of 2,186 subjects we found three SNPs (rs16969968, rs1051730, rs3743078) being associated with cognitive domains from the Wechsler-Adult-Intelligence Scale (WAIS-R)-most notably in the performance subtest "object assembly" and the verbal subtest "similarities." In a refined analysis of a subsample of 485 subjects, two of these three SNPs (rs16969968, rs1051730) were associated with n-back task performance/Continuous Performance Test. Furthermore, two CHRNA5 risk alleles (rs684513, rs637137) were associated with CHRNA5 mRNA expression levels in whole blood in a subgroup of 190 subjects. We here report for the first time an association of CHRNA5-CHRNA3-CHRNB4 gene variants with cognition possibly mediating in part risk for developing ND. The observed phenotype-genotype associations may depend on altered levels of gene expression. © 2010 Wiley-Liss, Inc.

摘要

最近的研究强烈支持烟碱型乙酰胆碱受体基因簇 CHRNA5-CHRNA3-CHRNB4 与尼古丁依赖(ND)之间存在关联。然而,确切的基因型-表型关系尚不清楚。有关吸烟行为的临床和流行病学数据提出了这样一种可能性,即相关的基因变异可能通过影响某些因“认知增强”而摄入尼古丁的吸烟者的认知表现,间接促成 ND 的发展。在这里,我们测试了 CHRNA5-CHRNA3-CHRNB4 基因簇中的七个单核苷酸多态性(SNP)rs684513、rs637137、rs16969968、rs578776、rs1051730、rs3743078、rs3813567 与 ND、认知表现和基因表达的关联。正如预期的那样,我们在包含 5561 个人的三个独立队列(KORA、NCOOP、ESTHER)中发现所有 SNP 都与 ND 相关。在 2186 名重叠样本中,我们发现三个 SNP(rs16969968、rs1051730、rs3743078)与 Wechsler 成人智力量表(WAIS-R)的认知领域相关,尤其是在表现测验“物体组装”和言语测验“相似性”中。在 485 名受试者的亚样本的精细分析中,这三个 SNP 中的两个(rs16969968、rs1051730)与 n-back 任务表现/连续性能测试相关。此外,在 190 名受试者的亚组中,两个 CHRNA5 风险等位基因(rs684513、rs637137)与全血中的 CHRNA5 mRNA 表达水平相关。我们在这里首次报告了 CHRNA5-CHRNA3-CHRNB4 基因变异与认知的关联,这可能部分介导了发展 ND 的风险。观察到的表型-基因型关联可能取决于基因表达水平的改变。©2010 Wiley-Liss,Inc.

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[10]
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[2]
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Transl Psychiatry. 2024-11-6

[3]
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PLoS One. 2022

[4]
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Front Neurol. 2022-7-7

[5]
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Evol Bioinform Online. 2022-4-24

[6]
Linking the CHRNA5 SNP to drug abuse liability: From circuitry to cellular mechanisms.

Neuropharmacology. 2021-3-15

[7]
Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population.

EBioMedicine. 2020-7

[8]
Promoter IV-BDNF deficiency disturbs cholinergic gene expression of CHRNA5, CHRM2, and CHRM5: effects of drug and environmental treatments.

J Neurochem. 2017-10

[9]
A genetic variant within previously associated with inattention in boys with attention deficit hyperactivity disorder is associated with enhanced cognition in healthy adult males.

Brain Behav. 2017-2-9

[10]
Cannabinoid receptor 1 (CNR1) gene variant moderates neural index of cognitive disruption during nicotine withdrawal.

Genes Brain Behav. 2016-9

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