巨噬细胞移动抑制因子
单核苷酸多态性
SNP公司
基因型
人口
等位基因
遗传学
神经发生
生物
遗传关联
基因
医学
细胞因子
环境卫生
作者
Toshiyuki Shirai,Kenji Okazaki,Takaki Tanifuji,Ikuo Otsuka,Masao Miyachi,Shohei Okada,Ryota Shindo,Tadasu Horai,Kentaro Mouri,Motonori Takahashi,Takeshi Kondo,Yasuhiro Ueno,Akitoyo Hishimoto
摘要
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.
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