EGR3多态性是中国人群精神分裂症风险的潜在易感因素

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Genetic testing and molecular biomarkers Pub Date : 2024-04-01 DOI:10.1089/gtmb.2023.0562
Wen Bi, Jingjing Li, Mengqiu Xiong, Lubanga Nasifu, Mingjuan Tan, Ping Tai, Qing Jin, Lingyun Zhang, Chengbin Zhu, Bangshun He
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引用次数: 0

摘要

研究目的本研究旨在评估中国人群中单核苷酸多态性(SNPs)(EGR3 rs1996147;EGR4 rs3813226、rs6747506;ERBB3 rs2292238;ERBB4 rs707284、rs7560730)与精神分裂症(SZ)风险之间的关联。材料与方法:我们进行了一项病例对照研究,其中包括 248 名 SZ 患者和 236 名年龄和性别匹配的健康对照者。采用 Mass-array 平台检测所有 SNPs 的基因型。结果显示结果显示,EGR3 rs1996147 AA基因型与SZ风险的边缘降低有关(AA vs. GG:调整OR = 0.43,95% CI:0.18-1.02,p = 0.06)。然而,其他 SNP 与总体 SZ 风险之间没有发现明显的相关性。亚组分析也未显示所有 SNPs 与 SZ 风险之间存在任何显著关联。结论综上所述,本研究发现 EGR3 rs1996147 AA 基因型与 SZ 的边缘风险有关。
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EGR3 Polymorphism Is a Potential Susceptibility Factor of Schizophrenia Risk in a Chinese Population.
Objective: The purpose of this study was to evaluate the association between the single nucleotide polymorphisms (SNPs) (EGR3 rs1996147; EGR4 rs3813226, rs6747506; ERBB3 rs2292238; and ERBB4 rs707284, rs7560730) and the risk of schizophrenia (SZ) in a Chinese population. Materials and Methods: We conducted a case-control study, including 248 patients with SZ and 236 healthy controls matched for age and sex. The Mass-array platform was used to detect all the genotypes of the SNPs. Results: The results revealed that the EGR3 rs1996147 AA genotype was associated with borderline decreased SZ risk (AA vs. GG: adjusted OR = 0.43, 95% CI: 0.18-1.02, p = 0.06). However, no significant correlation was found between the other SNPs and overall SZ risk. Subgroup analysis also failed to show any significant association between all SNPs and the risk of SZ. Conclusion: In summary, this study revealed that the EGR3 rs1996147 AA genotype was associated with a borderline risk for SZ.
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来源期刊
CiteScore
2.50
自引率
7.10%
发文量
63
审稿时长
1 months
期刊介绍: Genetic Testing and Molecular Biomarkers is the leading peer-reviewed journal covering all aspects of human genetic testing including molecular biomarkers. The Journal provides a forum for the development of new technology; the application of testing to decision making in an increasingly varied set of clinical situations; ethical, legal, social, and economic aspects of genetic testing; and issues concerning effective genetic counseling. This is the definitive resource for researchers, clinicians, and scientists who develop, perform, and interpret genetic tests and their results. Genetic Testing and Molecular Biomarkers coverage includes: -Diagnosis across the life span- Risk assessment- Carrier detection in individuals, couples, and populations- Novel methods and new instrumentation for genetic testing- Results of molecular, biochemical, and cytogenetic testing- Genetic counseling
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