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MIR1279基因上游的一种多态性与系统性红斑狼疮患者心包炎的发生相关,并有助于确定这一并发症的遗传风险特征。

A polymorphism upstream MIR1279 gene is associated with pericarditis development in Systemic Lupus Erythematosus and contributes to definition of a genetic risk profile for this complication.

作者信息

Ciccacci C, Perricone C, Politi C, Rufini S, Ceccarelli F, Cipriano E, Alessandri C, Latini A, Valesini G, Novelli G, Conti F, Borgiani P

机构信息

1 Department of Biomedicine and Prevention, Genetics Section, School of Medicine, University of Rome Tor Vergata, Italy.

2 Lupus Clinic, Reumatologia, Dipartimento di Clinica e Terapia Medica, Sapienza Università di Roma, Italy.

出版信息

Lupus. 2017 Jul;26(8):841-848. doi: 10.1177/0961203316679528. Epub 2016 Nov 23.

Abstract

Recently, a study has shown that a polymorphism in the region of MIR1279 modulates the expression of the TRAF3IP2 gene. Since polymorphisms in the TRAF3IP2 gene have been described in association with systemic lupus erithematosus (SLE) susceptibility and with the development of pericarditis, our aim is to verify if the MIR1279 gene variability could also be involved. The rs1463335 SNP, located upstream MIR1279 gene, was analyzed by allelic discrimination assay in 315 Italian SLE patients and 201 healthy controls. Moreover, the MIR1279 gene was full sequenced in 50 patients. A case/control association study and a genotype/phenotype correlation analysis were performed. We also constructed a pericarditis genetic risk profile for patients with SLE. The full sequencing of the MIR1279 gene in patients with SLE did not reveal any novel or known variation. The variant allele of the rs1463335 SNP was significantly associated with susceptibility to pericarditis ( P = 0.017 and OR = 1.67). A risk profile model for pericarditis considering the risk alleles of MIR1279 and three other genes (STAT4, PTPN2 and TRAF3IP2) showed that patients with 4 or 5 risk alleles have a higher risk of developing pericarditis ( OR = 4.09 with P = 0.001 and OR = 6.04 with P = 0.04 respectively). In conclusion, we describe for the first time the contribution of a MIR1279 SNP in pericarditis development in patients with SLE and a genetic risk profile model that could be useful to identify patients more susceptible to developing pericarditis in SLE. This approach could help to improve the prediction and the management of this complication.

摘要

最近,一项研究表明,MIR1279区域的多态性可调节TRAF3IP2基因的表达。由于已报道TRAF3IP2基因的多态性与系统性红斑狼疮(SLE)易感性以及心包炎的发生有关,我们的目的是验证MIR1279基因变异是否也与之相关。通过等位基因鉴别分析,对315名意大利SLE患者和201名健康对照者分析了位于MIR1279基因上游的rs1463335单核苷酸多态性(SNP)。此外,对50名患者的MIR1279基因进行了全序列测定。进行了病例/对照关联研究和基因型/表型相关性分析。我们还为SLE患者构建了心包炎遗传风险图谱。SLE患者MIR1279基因的全序列测定未发现任何新的或已知的变异。rs1463335 SNP的变异等位基因与心包炎易感性显著相关(P = 0.017,比值比[OR]=1.67)。一个考虑MIR1279和其他三个基因(STAT4、PTPN2和TRAF3IP2)风险等位基因的心包炎风险图谱模型显示,具有4个或5个风险等位基因的患者发生心包炎的风险更高(OR分别为4.09,P = 0.001;OR为6.04,P = 0.04)。总之,我们首次描述了MIR1279 SNP在SLE患者心包炎发生中的作用以及一个遗传风险图谱模型,该模型可能有助于识别SLE中更易发生心包炎的患者。这种方法有助于改善对该并发症的预测和管理。

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