首页> 美国卫生研究院文献>Mediators of Inflammation >Lack of Association between ABO PPAP2B ADAMST7 PIK3CG and EDNRA and Carotid Intima-Media Thickness Carotid Plaques and Cardiovascular Disease in Patients with Rheumatoid Arthritis
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Lack of Association between ABO PPAP2B ADAMST7 PIK3CG and EDNRA and Carotid Intima-Media Thickness Carotid Plaques and Cardiovascular Disease in Patients with Rheumatoid Arthritis

机译:类风湿关节炎患者中ABOPPAP2BADAMST7PIK3CG和EDNRA与颈动脉内膜中层厚度颈动脉斑块和心血管疾病之间缺乏关联

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摘要

Introduction. Rheumatoid arthritis (RA) is a polygenic disease associated with accelerated atherosclerosis and increased cardiovascular (CV) mortality. Recent studies have identified the ABO rs579459, PPAP2B rs17114036, and ADAMTS7 rs3825807 polymorphisms as genetic variants associated with coronary artery disease and the PIK3CG rs17398575 and EDNRA rs1878406 polymorphisms as the most significant signals related to the presence of carotid plaque in nonrheumatic Caucasian individuals. Accordingly, we evaluated the potential relationship between these 5 polymorphisms and subclinical atherosclerosis (assessed by carotid intima-media thickness (cIMT) and presence/absence of carotid plaques) and CV disease in RA. Material and Methods. 2140 Spanish RA patients were genotyped for the 5 polymorphisms by TaqMan assays. Subclinical atherosclerosis was evaluated in 620 of these patients by carotid ultrasonography technology. Results. No statistically significant differences were found when each polymorphism was assessed according to cIMT values and presence/absence of carotid plaques in RA, after adjusting the results for potential confounders. Moreover, no significant differences were obtained when RA patients were stratified according to the presence/absence of CV disease after adjusting for potential confounders. Conclusion. Our results do not confirm association between ABO rs579459, PPAP2B rs17114036, ADAMTS7 rs3825807, PIK3CG rs17398575, and EDNRA rs1878406 and subclinical atherosclerosis and CV disease in RA.
机译:介绍。类风湿关节炎(RA)是与动脉粥样硬化加速和心血管(CV)死亡率增加相关的多基因疾病。最近的研究已经确定ABO rs579459,PPAP2B rs17114036和ADAMTS7 rs3825807多态性是与冠心病相关的遗传变异,而PIK3CG rs17398575和EDNRA rs1878406多态性是与非风湿性白种人个体中颈动脉斑块相关的最重要信号。因此,我们评估了这5种多态性与亚临床动脉粥样硬化(通过颈动脉内膜中层厚度(cIMT)和颈动脉斑块的存在与否)和CV疾病之间的潜在关系。材料与方法。通过TaqMan分析对2140名西班牙RA患者的5种多态性进行了基因分型。通过颈动脉超声技术评估了这些患者中的620例亚临床动脉粥样硬化。结果。调整潜在混杂因素的结果后,根据cIMT值和RA中颈动脉斑块的存在与否评估每种多态性时,没有发现统计学上的显着差异。而且,在对RA患者进行了潜在混杂因素调整后,根据CV疾病的存在/不存在对RA患者进行分层时,没有发现显着差异。结论。我们的结果未证实RA中ABO rs579459,PPAP2B rs17114036,ADAMTS7 rs3825807,PIK3CG rs17398575和EDNRA rs1878406与RA的亚临床动脉粥样硬化和CV疾病之间存在关联。

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