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类风湿关节炎患者中,9p21.3基因组区域的单核苷酸多态性与心血管疾病风险无关。

Single-nucleotide polymorphisms at the 9p21.3 genomic region not associated with the risk of cardiovascular disease in patients with rheumatoid arthritis.

作者信息

García-Bermúdez M, López-Mejías R, Genre F, Castañeda S, González-Juanatey C, Llorca J, Corrales A, Miranda-Filloy J A, Pina T, Gómez-Vaquero C, Rodríguez-Rodríguez L, Fernández-Gutiérrez B, Pascual-Salcedo D, Balsa A, López-Longo F J, Carreira P, Blanco R, González-Álvaro I, Martín J, González-Gay M A

机构信息

Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, 18016, Granada, Spain.

出版信息

Tissue Antigens. 2013 Dec;82(6):405-9. doi: 10.1111/tan.12227. Epub 2013 Oct 15.

Abstract

Rheumatoid arthritis (RA) is a chronic polygenic inflammatory disease associated with accelerated atherosclerosis and high risk of cardiovascular disease (CVD). In this study, we evaluated the potential association of 9p21.3 single-nucleotide polymorphisms (SNPs) - previously linked to coronary artery disease - and CVD risk in 2001 Spanish RA patients genotyped for 9p21.3 SNPs using TaqMan™ assays. Carotid intima media thickness (cIMT) and presence of carotid plaques were also analyzed. Cox regression model did not disclose significant differences between patients who experienced CVD and those who did not. Neither association was found between cIMT or carotid plaques and SNPs allele distribution. In conclusion, results do not support a role of rs10116277 or rs1537375 SNPs in CVD risk in Spanish RA patients.

摘要

类风湿性关节炎(RA)是一种慢性多基因炎症性疾病,与动脉粥样硬化加速和心血管疾病(CVD)高风险相关。在本研究中,我们使用TaqMan™分析对2001名西班牙RA患者进行了9p21.3单核苷酸多态性(SNP)基因分型,这些SNP先前与冠状动脉疾病相关,我们评估了其与CVD风险的潜在关联。还分析了颈动脉内膜中层厚度(cIMT)和颈动脉斑块的存在情况。Cox回归模型未揭示发生CVD的患者与未发生CVD的患者之间存在显著差异。在cIMT或颈动脉斑块与SNP等位基因分布之间也未发现关联。总之,结果不支持rs10116277或rs1537375 SNP在西班牙RA患者CVD风险中起作用。

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