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NRAMP1/SLC11A1基因变体D543N(1730G/A)在墨西哥梅斯蒂索人群类风湿关节炎遗传易感性中的作用

The Role of NRAMP1/SLC11A1 Gene Variant D543N (1730G/A) in the Genetic Susceptibility to Develop Rheumatoid Arthritis in the Mexican Mestizo population.

作者信息

Niño-Moreno Perla, Turrubiartes-Martínez Edgar, Oceguera-Maldonado Brenda, Baltazar-Benítez Nubia, Negrete-González Cindy, Oliva-Ramírez Brenda, Baranda Lourdes, González-Amaro Roberto

机构信息

Laboratory of Genetics and Molecular Diagnostics, Faculty of Chemical Sciences, Universidad Autónoma de San Luis Potosí, San Luis Potosí, S.L.P., Mexico.

Research Center for Health Sciences and Biomedicine, Universidad Autónoma de San Luis Potosí, San Luis Potosí, S.L.P., Mexico.

出版信息

Rev Invest Clin. 2017 Jan-Feb;69(1):5-10. doi: 10.24875/ric.17002152.

Abstract

BACKGROUND

Rheumatoid arthritis is a chronic inflammatory disease whose cause has not been fully elucidated. However, genetic factors seem to have an important role in its pathogenesis.

OBJECTIVE

We analyzed the possible association between rheumatoid arthritis and variants of the SLC11A1 gene, which encodes for NRAMP1, a protein involved in the activation of phagocytes and synthesis of proinflammatory cytokines.

METHODS

In a case-control study in a Mexican Mestizo population, blood samples from 188 patients with rheumatoid arthritis and 133 healthy individuals were obtained to determine the frequency of SLC11A1 gene variants INT4 (469+14G/C or rs3731865), D543N (1730G/A or rs17235409) and 3'UTR (1729+55del4 or rs17235416) by polymerase chain reaction and restriction fragment length polymorphism.

RESULTS

We found similar frequencies of INT4 and 3'UTR polymorphisms in patients and controls (p = 0.18 and 0.89, respectively). In contrast, a significantly lower frequency of the D543N polymorphism was observed in patients with rheumatoid arthritis compared to controls (p corrected = 0.016; OR: 0.48; 95% CI: 0.28-0.80).

CONCLUSION

Our data suggest that the D543N variant of SLC11A1 gene has a protective effect in the development of rheumatoid arthritis, an interesting finding that has not been previously reported in any population.

摘要

背景

类风湿性关节炎是一种慢性炎症性疾病,其病因尚未完全阐明。然而,遗传因素似乎在其发病机制中起重要作用。

目的

我们分析了类风湿性关节炎与SLC11A1基因变异之间的可能关联,该基因编码NRAMP1,一种参与吞噬细胞激活和促炎细胞因子合成的蛋白质。

方法

在一项针对墨西哥梅斯蒂索人群的病例对照研究中,采集了188例类风湿性关节炎患者和133名健康个体的血样,通过聚合酶链反应和限制性片段长度多态性来确定SLC11A1基因变异INT4(469 + 14G/C或rs3731865)、D543N(1730G/A或rs17235409)和3'UTR(1729 + 55del4或rs17235416)的频率。

结果

我们发现患者和对照组中INT4和3'UTR多态性的频率相似(分别为p = 0.18和0.89)。相比之下,与对照组相比,类风湿性关节炎患者中D543N多态性的频率显著更低(校正p = 0.016;OR:0.48;95% CI:0.28 - 0.80)。

结论

我们的数据表明,SLC11A1基因的D543N变异在类风湿性关节炎的发生发展中具有保护作用,这一有趣的发现此前在任何人群中均未报道过。

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