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巨噬细胞移动抑制因子基因启动子低氧反应元件单核苷酸多态性与日本人群自杀完成者的关联研究。

Association study of a single nucleotide polymorphism in the hypoxia response element of the macrophage migration inhibitory factor gene promoter with suicide completers in the Japanese population.

作者信息

Shirai Toshiyuki, Okazaki Satoshi, Tanifuji Takaki, Otsuka Ikuo, Miyachi Masao, Okada Shohei, Shindo Ryota, Horai Tadasu, Mouri Kentaro, Takahashi Motonori, Kondo Takeshi, Ueno Yasuhiro, Hishimoto Akitoyo

机构信息

Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.

Division of Legal Medicine, Department of Community Medicine and Social Health Science, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

Neuropsychopharmacol Rep. 2024 Mar;44(1):262-266. doi: 10.1002/npr2.12410. Epub 2024 Jan 24.

Abstract

BACKGROUND

More than 800 000 people die by suicide annually. The heritability of suicide is 30%-50%. We focused on the hypoxia response element (HRE), which promotes the expression of macrophage migration inhibitory factor (MIF) via the hypoxia-inducible factor (HIF) pathway, important in neurogenesis and neuroprotection. We examined a genetic polymorphism of rs17004038, a single-nucleotide polymorphism (SNP), in suicide completers and controls.

METHODS

The study population included 1336 suicide completers and 814 unrelated healthy controls. All participants were Japanese. We obtained peripheral blood, extracted DNA, and genotyped the patients for SNP rs17004038 (C > A).

RESULTS

No significant differences were observed between the two groups in either the allele or genotype analyses. Subgroup analyses by sex, age (<40 or ≥40), and suicide method (violent or nonviolent suicide) were performed with similar results.

CONCLUSION

No association was observed between SNP rs17004038 and suicide completion. Although it is challenging to collect a large number of samples from suicide completers, further MIF-related genetic studies, including those of rs17004038, are necessary with larger sample sizes.

摘要

背景

每年有超过80万人死于自杀。自杀的遗传率为30%-50%。我们聚焦于缺氧反应元件(HRE),其通过缺氧诱导因子(HIF)途径促进巨噬细胞移动抑制因子(MIF)的表达,这在神经发生和神经保护中很重要。我们研究了自杀死亡者和对照组中rs17004038的基因多态性,这是一种单核苷酸多态性(SNP)。

方法

研究人群包括1336例自杀死亡者和814名无亲缘关系的健康对照者。所有参与者均为日本人。我们采集外周血,提取DNA,并对患者进行SNP rs17004038(C>A)基因分型。

结果

在等位基因或基因型分析中,两组之间均未观察到显著差异。按性别、年龄(<40岁或≥40岁)和自杀方式(暴力或非暴力自杀)进行亚组分析,结果相似。

结论

未观察到SNP rs17004038与自杀死亡之间存在关联。尽管从自杀死亡者中收集大量样本具有挑战性,但有必要对包括rs17004038在内的与MIF相关的基因进行更大样本量的进一步研究。

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