韩国酒精依赖患者的FYN酪氨酸激酶基因多态性

IF 1.3 Q3 PSYCHIATRY
Alpha psychiatry Pub Date : 2025-02-28 eCollection Date: 2025-02-01 DOI:10.31083/AP38752
Sung Young Huh, Sung-Gon Kim, Ji-Hoon Kim, Hyeon-Kyeong Kim, Yeon-Sue Kim
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引用次数: 0

摘要

背景:酒精使用障碍(AUD)是一种经济成本较高的常见病。与酒精相关的谷氨酸细胞信号通路已被报道为AUD的主要病理之一。先前的研究表明FYN可能与AUD有关,FYN通过磷酸化控制NMDA谷氨酸受体的功能。方法:本研究纳入酒精依赖组354例,对照组139例。酒精依赖组是从5所大学医院和1所精神病院招募的,对照组是从到国内大学医院进行常规体检的人中招募的。FYN基因单核苷酸多态性(single nucleotide polymorphism, SNP)是根据SNP数据库和FYN基因的既往研究筛选出的。采用聚合酶链反应-限制性片段长度多态性技术对10个snp进行基因分型。结果:男性AUD患者rs1058134的GG基因型和G等位基因频率显著低于对照组(p = 0.003)。女性AUD患者rs12191154的AA基因型和A等位基因频率显著低于对照组(p < 0.001, p = 0.003)。女性AUD患者rs9387025的AA基因型和A等位基因频率显著高于对照组(p = 0.003)。结论:这些发现提示FYN基因可能是AUD的候选基因。这可能有助于规划进一步的研究,以确定每个SNP的功能以及FYN基因与AUD之间的确切关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FYN Tyrosine Kinase Gene Polymorphisms in Alcohol-Dependent Korean Patients.

Background: Alcohol use disorder (AUD) is a common disease with a high economic cost. The glutamate cell signaling pathway associated with alcohol has been reported to be one of the main pathologies of AUD. Previous studies have suggested that FYN, which is known to control NMDA glutamate receptor function through phosphorylation, might be associated with AUD.

Method: The present study included 354 subjects in the alcohol-dependent group and 139 subjects in the control group. The alcohol-dependent group was recruited from five university hospitals and a psychiatric hospital, and the control group was recruited from people who visited the university hospital for routine medical checkups in Korea. FYN gene single nucleotide polymorphism (SNPs) were selected based on SNP databases and previous studies of the FYN gene. Ten SNPs were genotyped using polymerase chain reaction-restriction fragment length polymorphism techniques.

Results: GG genotypes and G allele frequencies of rs1058134 in male AUD patients were significantly lower than in controls (p = 0.003). AA genotypes and A allele frequencies of rs12191154 in female AUD patients were significantly lower than in controls (p < 0.001, p = 0.003). In female AUD patients, AA genotypes and A allele frequencies of rs9387025 were significantly higher than in controls (p = 0.003).

Conclusion: These findings suggest that the FYN gene may be a candidate gene for AUD. This may help for the planning of further studies to determine the function of each SNP and the exact relationship between the FYN gene and AUD.

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