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白细胞介素-1β的基因变异性作为创伤后应激障碍发生的潜在因素。

Genetic variability of interleukin-1 beta as prospective factor from developing post-traumatic stress disorder.

作者信息

Hovhannisyan Lilit, Stepanyan Ani, Arakelyan Arsen

机构信息

Institute of Molecular Biology, Armenian National Academy of Sciences, Hasratyan 7 street, 0014, Yerevan, Armenia.

出版信息

Immunogenetics. 2017 Oct;69(10):703-708. doi: 10.1007/s00251-017-1016-4. Epub 2017 Jul 5.

Abstract

Individual susceptibility to post-traumatic stress disorder (PTSD) is conditioned by genetic factors, and association between this disorder and polymorphisms of several genes have been shown. The aim of this study was to explore a potential association between single nucleotide polymorphisms (SNP) of the IL-1β gene (IL1B) and PTSD. In genomic DNA samples of PTSD-affected and healthy subjects, the rs16944, rs1143634, rs2853550, rs1143643, and rs1143633 SNPs of IL1B gene have been genotyped. The results obtained demonstrated that IL1B rs1143633C and rs16944A minor allele frequency were significantly lower in patients than in controls. Our results confirm that IL1B rs1143633 and rs16944 SNPs are negatively associated with PTSD which allows us to consider them as protective variants for PTSD. IL1B rs1143633C and rs16944A minor allele frequencies and carriage rates are significantly lower in the PTSD patients as compared to the controls. These results may provide a base to conclude that above-mentioned alleles can be protective against PTSD, and IL1B gene can be involved in the pathogenesis of this disorder.

摘要

个体对创伤后应激障碍(PTSD)的易感性受遗传因素影响,且该障碍与多个基因的多态性之间已显示存在关联。本研究的目的是探讨白细胞介素-1β基因(IL-1β,IL1B)的单核苷酸多态性(SNP)与创伤后应激障碍之间的潜在关联。在创伤后应激障碍患者和健康受试者的基因组DNA样本中,对IL1B基因的rs16944、rs1143634、rs2853550、rs1143643和rs1143633单核苷酸多态性进行了基因分型。所得结果表明,患者中IL1B rs1143633C和rs16944A的次要等位基因频率显著低于对照组。我们的结果证实,IL1B rs1143633和rs16944单核苷酸多态性与创伤后应激障碍呈负相关,这使我们能够将它们视为创伤后应激障碍的保护性变异。与对照组相比,创伤后应激障碍患者中IL1B rs1143633C和rs16944A的次要等位基因频率和携带率显著更低。这些结果可能为得出上述等位基因可预防创伤后应激障碍以及IL1B基因可能参与该障碍的发病机制这一结论提供依据。

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