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干扰素调节因子5基因变异体rs2004640和rs4728142与类风湿关节炎患者的颈动脉内膜中层厚度相关,但与心血管事件无关。

Interferon regulatory factor 5 gene variants rs2004640 and rs4728142 are associated with carotid intima media thickness but not with cardiovascular events in rheumatoid arthritis.

作者信息

Agca Rabia, van Sijl Alper M, Vosslamber Saskia, Voskuyl Alexandre E, Verweij Cor L, Nurmohamed Michael T

机构信息

Amsterdam Rheumatology and Immunology Center, Department of Rheumatology, location Reade and location VU University Medical Center, Amsterdam, The Netherlands.

Department of Pathology, Amsterdam University Medical Centers, location VU University Medical Center, Amsterdam, The Netherlands.

出版信息

Clin Exp Rheumatol. 2022 Jan;40(1):64-68. doi: 10.55563/clinexprheumatol/pf511x. Epub 2021 Mar 2.

Abstract

OBJECTIVES

Rheumatoid arthritis (RA) is associated with cardiovascular (CV) morbidity and mortality. Interferon regulatory factor 5 (IRF5) gene polymorphisms rs2004640 and rs4728142 have been associated with autoimmune diseases, but also with atherosclerosis. Differences in IRF5 gene expression can lead to the production of different interferons and might play a role in the atherogenic process in RA.

METHODS

We investigated the effects of IRF5 gene variants rs2004640 and rs4728142 on clinical parameters related to atherosclerosis, such as cIMT (in subgroup n=101), and new CV events (in whole cohort n=353).

RESULTS

For rs2004640, cIMT values at baseline were highest within the group of patients carrying the GG-genotype, followed by GT- and TT- genotypes, which was statistically significant. Over time patients with the TT-genotype had the highest increase in cIMT. For rs4728142 cIMT values were also the highest for patients with the GG-genotype at baseline, but the difference between the groups was not statistically significant. Over time the highest increase in cIMT was in the patients with the AA-genotype. Both rs2004640 and rs4728142 were not associated with new CV events during follow-up.

CONCLUSIONS

IRF5 alleles are associated with changes in cIMT, but not with new CV events in RA. Although these findings implicate a role of the IRF5 transcription pathway in atherosclerosis, IRF5 single nucleotide polymorphisms do not appear to increase the risk of future CV events.

摘要

目的

类风湿关节炎(RA)与心血管(CV)疾病的发病率和死亡率相关。干扰素调节因子5(IRF5)基因多态性rs2004640和rs4728142不仅与自身免疫性疾病有关,还与动脉粥样硬化有关。IRF5基因表达的差异可导致产生不同的干扰素,并可能在RA的动脉粥样硬化形成过程中发挥作用。

方法

我们研究了IRF5基因变异rs2004640和rs4728142对与动脉粥样硬化相关的临床参数的影响,如颈动脉内膜中层厚度(cIMT,亚组n = 101),以及新发CV事件(整个队列n = 353)。

结果

对于rs2004640,携带GG基因型的患者组基线时的cIMT值最高,其次是GT和TT基因型,差异具有统计学意义。随着时间的推移,TT基因型患者的cIMT增加最多。对于rs4728142,基线时GG基因型患者的cIMT值也最高,但组间差异无统计学意义。随着时间的推移,AA基因型患者的cIMT增加最多。rs2004640和rs4728142均与随访期间的新发CV事件无关。

结论

IRF5等位基因与cIMT的变化有关,但与RA患者的新发CV事件无关。尽管这些发现表明IRF5转录途径在动脉粥样硬化中起作用,但IRF5单核苷酸多态性似乎不会增加未来CV事件的风险。

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