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重度抑郁症与血清素2A受体基因-1438A/G多态性之间的关联。

Association between major depressive disorder and the -1438A/G polymorphism of the serotonin 2A receptor gene.

作者信息

Choi Myoung-Jin, Lee Heon-Jeong, Lee Hye-Jin, Ham Byung-Joo, Cha Ji-Hyun, Ryu Seung-Ho, Lee Min-Soo

机构信息

Department of Psychiatry, Korea University College of Medicine, Seoul, Korea.

出版信息

Neuropsychobiology. 2004;49(1):38-41. doi: 10.1159/000075337.

Abstract

This study investigated the possible effect of the -1438A/G single-nucleotide polymorphism in the promoter region of the serotonin 2A receptor (5-HTR2A) gene on major depressive disorder (MDD) in a Korean population. This polymorphism was analyzed in 189 patients with MDD and in 148 unrelated healthy controls using a case-control design, which revealed a significant difference in the genotype distributions (chi(2) = 10.78, d.f. = 2, p = 0.005). The frequency of the -1438G allele was also much higher in MDD patients than in normal controls (chi(2) = 7.20, p = 0.007; OR = 1.52, 95% CI 1.12-2.06). We also found significantly more carriers of the G allele (GG+AG genotypes) in MDD patients than in normal controls (chi(2) = 10.18, p = 0.001; OR = 2.46, 95% CI 1.40-4.32). Our results support the hypothesis that the -1438A/G polymorphism of the promoter region of the 5-HTR2A gene is associated with MDD patients in a Korean population.

摘要

本研究调查了韩国人群中血清素2A受体(5-HTR2A)基因启动子区域-1438A/G单核苷酸多态性对重度抑郁症(MDD)的可能影响。采用病例对照设计,对189例MDD患者和148名无亲缘关系的健康对照者进行了该多态性分析,结果显示基因型分布存在显著差异(χ² = 10.78,自由度 = 2,p = 0.005)。MDD患者中-1438G等位基因的频率也远高于正常对照者(χ² = 7.20,p = 0.007;OR = 1.52,95% CI 1.12 - 2.06)。我们还发现,MDD患者中G等位基因携带者(GG + AG基因型)明显多于正常对照者(χ² = 10.18,p = 0.001;OR = 2.46,95% CI 1.40 - 4.32)。我们的结果支持这样的假设,即5-HTR2A基因启动子区域的-1438A/G多态性与韩国人群中的MDD患者相关。

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