M. N. Drehmer, Gabriel Vaisam Castro, I. Pereira, Iliada Rainha de Souza Sara Emelie Lofgren
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引用次数: 0
摘要
目的:一些证据表明雌激素通路在几种自身免疫相关反应和疾病中起关键作用。本研究的目的是研究ESR1基因变异与RA易感性的关系,并将分析扩展到巴西患者样本中RA的特定临床表现。方法:采用Taqman SNP探针对449例患者(健康对照268例,RA患者181例)进行ESR1基因rs2234693多态性分型。患者组由153名女性和28名男性组成。采用SPSS软件进行logistic回归分析。结果:rs2234693变异与男性和女性RA相关(rs2234693- cc基因型OR = 2.21, p = 0.0032)。rs2234693-CC基因型还与心脏病(OR = 2.40, p = 0.025)、高血压(OR = 2.50, p = 0.019)和骨质疏松症(OR = 1.94, p = 0.031)的存在以及抗ccp抗体(rs2234693-C等位基因OR= 1.91, p = 0.024)的存在相关。结论:ESR1与RA相关,也与抗ccp抗体的存在以及与RA相关的特殊临床表现(心脏病、高血压和骨质疏松症)有关。我们的研究首次提供了ESR1变异与RA之间关联的证据。
Estrogen receptor alpha gene (ESR1)variant is associated with rheumatoidarthritis susceptibility and to particularclinical manifestations of the disease
Objective: Several lines of evidence suggest a pivotal role of the estrogen pathway in several autoimmune-related responses and disease. The aim of this study was to investigate the association of a variant in ESR1 gene with RA susceptibility and expand the analysis to specific clinical manifestations of RA in a sample of Brazilian patients. Methods: 449 individuals (268 healthy controls and 181 RA patients) were genotyped for the polymorphism rs2234693 in the ESR1 gene with Taqman SNP probes. The patient’s group was composed by 153 female and 28 men. Association analysis were performed by logistic regression using SPSS software. Results: The rs2234693 variant is associated with RA in males and females (rs2234693-CC genotype OR = 2.21, p = 0.0032). The rs2234693-CC genotype was also associated with the presence of cardiopathy (OR = 2.40, p = 0.025), high blood pressure (OR = 2.50, p = 0.019) and osteoporosis (OR = 1.94, p = 0.031), and also with the presence of anti-CCP antibodies (rs2234693-C allele OR= 1.91, p = 0.024). Conclusion: ESR1 is associated with RA, as well as with the presence of anti-CCP antibodies and particularRA-associated clinical manifestations (cardiopathy, high blood pressure and osteoporosis). Our study presents the first evidence of association between ESR1 variant and RA.