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维生素 D 受体基因多态性与巴西南部的麻风病有关。

Vitamin D Receptor Gene Polymorphisms Are Associated With Leprosy in Southern Brazil.

机构信息

Laboratory of Immunogenetics, Department of Basic Health Sciences, Maringá State University (UEM), Maringá, Brazil.

Department of Medicine, Faculty of Medical Sciences, Campinas State University (UNICAMP), São Paulo, Brazil.

出版信息

Front Immunol. 2019 Oct 4;10:2157. doi: 10.3389/fimmu.2019.02157. eCollection 2019.

Abstract

Vitamin D, together with its nuclear receptor (VDR), plays an important role in modulating the immune response, decreasing the inflammatory process. Some polymorphisms of the gene, such as I (G>A rs1544410)I (G>T rs7975232), and I (T>C rs731236) could affect its stability and mRNA transcription activity, while I T>C (rs2228570) gives a truncated protein with three fewer amino acids and more efficiency in binding vitamin D. This study evaluated these four polymorphisms in the immunopathogenesis of leprosy in 404 patients and 432 control individuals without chronic or infectious disease in southern Brazil. When analyzing differences in the allele and genotype frequency of polymorphisms between patients (leprosy , multibacillary, and paucibacillary clinical forms) and controls, we found no statistically significant association. Regarding haplotype analysis, the bAt haplotype was associated with protection from leprosy ( = 0.004, OR = 0.34, CI = 0.16-0.71) and from the multibacillary clinical form ( = 0.005, OR = 0.30, CI = 0.13-0.70). In individuals aged 40 or more years, this haplotype has also showed protection against leprosy and multibacillary (OR = 0.26, CI = 0.09-0.76; OR = 0.26, CI = 0.07-0.78, respectively), while the BAt haplotype was a risk factor for leprosy in the same age group (OR = 1.34, CI = 1.04-1.73). In conclusion, despite having found no associations between the gene polymorphisms with the development of leprosy, the haplotypes formed by the I, I, and I polymorphisms were associated with leprosy and the multibacillary clinical form.

摘要

维生素 D 与其核受体(VDR)一起,在调节免疫反应、减少炎症过程方面发挥着重要作用。基因的一些多态性,如 I(G>A rs1544410)I(G>T rs7975232)和 I(T>C rs731236),可能会影响其稳定性和 mRNA 转录活性,而 I T>C(rs2228570)则会产生一个截断蛋白,少三个氨基酸,与维生素 D 的结合效率更高。本研究在巴西南部评估了这四个多态性在麻风病的免疫发病机制中的作用,共纳入 404 例患者和 432 例无慢性或传染性疾病的对照个体。在分析患者(麻风病、多菌型和少菌型临床形式)和对照组之间多态性等位基因和基因型频率的差异时,我们未发现统计学显著关联。至于单体型分析,bAt 单体型与麻风病(=0.004,OR=0.34,CI=0.16-0.71)和多菌型临床形式(=0.005,OR=0.30,CI=0.13-0.70)的保护有关。在 40 岁或以上的个体中,该单体型也对麻风病和多菌型具有保护作用(OR=0.26,CI=0.09-0.76;OR=0.26,CI=0.07-0.78),而 BAt 单体型则是该年龄组麻风病的危险因素(OR=1.34,CI=1.04-1.73)。综上所述,尽管我们未发现基因多态性与麻风病发展之间存在关联,但由 I、I 和 I 多态性形成的单体型与麻风病和多菌型临床形式有关。

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