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巨噬细胞移动抑制因子基因多态性(SNP-173 G>C 和 STR-794 CATT5-8)与斑块状银屑病发病风险相关:一项病例对照研究。

Macrophage migration inhibitory factor gene polymorphisms (SNP -173 G>C and STR-794 CATT5-8) confer risk of plaque psoriasis: A case-control study.

机构信息

Instituto de Investigación en Ciencias Biomédicas, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.

Dermika Centro Dermatológico y Láser. Vallarta Nte, Guadalajara, Jalisco, Mexico.

出版信息

J Clin Lab Anal. 2021 Nov;35(11):e23999. doi: 10.1002/jcla.23999. Epub 2021 Sep 17.

DOI:10.1002/jcla.23999
PMID:34533238
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8605153/
Abstract

BACKGROUND

Macrophage inhibitory factor (MIF) is a pro-inflammatory cytokine secreted by several cells, including those in the immune system and the skin. The MIF gene contains the SNP -173 G> C and STR -794 CATT polymorphisms in the promoter region capable of affecting its activity. Our objective was to investigate the MIF polymorphisms as a risk factor for plaque psoriasis (PP) in the Mexican population.

METHODS

We genotyped both MIF polymorphism (rs5844572 and rs755622) in 224 PP patients with a clinical and histopathological diagnosis and 232 control subjects (CS) by the PCR-RFLP method. MIF serum levels were determined by an ELISA kit.

RESULTS

We found significant differences in the genotypic and allelic frequencies for the MIF -173 G>C polymorphism; carriers of the GC genotype (OR 1.51, 95% CI 1.026-2.228, p = 0.03) and the C allele (OR 1.34, 95% CI 1.005-1.807, p = 0.04) had higher odds to present with PP. Moreover, the 6C haplotype was associated with PP risk (OR 2.10, 95% CI 1.22-3.69, p < 0.01). Also, the -173 CC genotype was associated with high MIF serum levels (p < 0.05).

CONCLUSIONS

The -173 GC genotype and the 6C haplotype of the MIF polymorphisms are associated with susceptibility to PP in the Mexican population.

摘要

背景

巨噬细胞抑制因子(MIF)是一种由多种细胞分泌的促炎细胞因子,包括免疫系统和皮肤中的细胞。MIF 基因在启动子区域包含 SNP-173 G>C 和 STR-794 CATT 多态性,这些多态性能够影响其活性。我们的目的是研究 MIF 多态性作为墨西哥人群斑块状银屑病(PP)的风险因素。

方法

我们通过 PCR-RFLP 方法对 224 例具有临床和组织病理学诊断的 PP 患者和 232 例对照(CS)进行了 MIF 多态性(rs5844572 和 rs755622)的基因分型。通过 ELISA 试剂盒测定 MIF 血清水平。

结果

我们发现 MIF-173 G>C 多态性的基因型和等位基因频率存在显著差异;GC 基因型(OR 1.51,95%CI 1.026-2.228,p=0.03)和 C 等位基因(OR 1.34,95%CI 1.005-1.807,p=0.04)携带者发生 PP 的可能性更高。此外,6C 单倍型与 PP 风险相关(OR 2.10,95%CI 1.22-3.69,p<0.01)。此外,-173 CC 基因型与高 MIF 血清水平相关(p<0.05)。

结论

MIF 多态性的-173 GC 基因型和 6C 单倍型与墨西哥人群中 PP 的易感性相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/b9b330a4eff1/JCLA-35-e23999-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/a46f5fc87149/JCLA-35-e23999-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/15733d7e66d5/JCLA-35-e23999-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/38abbd133eed/JCLA-35-e23999-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/b9b330a4eff1/JCLA-35-e23999-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/a46f5fc87149/JCLA-35-e23999-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/15733d7e66d5/JCLA-35-e23999-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/38abbd133eed/JCLA-35-e23999-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e7b/8605153/b9b330a4eff1/JCLA-35-e23999-g002.jpg

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