首页> 外文期刊>Mediators of inflammation >Lack of Association betweenABO,PPAP2B,ADAMST7,PIK3CG, andEDNRAand Carotid Intima-Media Thickness, Carotid Plaques, and Cardiovascular Disease in Patients with Rheumatoid Arthritis
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Lack of Association betweenABO,PPAP2B,ADAMST7,PIK3CG, andEDNRAand Carotid Intima-Media Thickness, Carotid Plaques, and Cardiovascular Disease in Patients with Rheumatoid Arthritis

机译:类风湿关节炎患者缺乏ABO,PPAP2B,ADAMST7,PIK3CG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的联系

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Introduction. Rheumatoid arthritis (RA) is a polygenic disease associated with accelerated atherosclerosis and increased cardiovascular (CV) mortality. Recent studies have identified theABOrs579459,PPAP2Brs17114036, andADAMTS7rs3825807 polymorphisms as genetic variants associated with coronary artery disease and thePIK3CGrs17398575 andEDNRArs1878406 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 betweenABOrs579459,PPAP2Brs17114036,ADAMTS7rs3825807,PIK3CGrs17398575, andEDNRArs1878406 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。最近的研究已确定ABOrs579459,PPAP2Brs17114036和ADAMTS7rs3825807多态性为与冠心病相关的遗传变异,而PIK3CGrs17398575和EDNRArs1878406多态性为与非风湿性白种人个体中颈动脉斑块存在相关的最重要信号。因此,我们评估了RA中这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。通过颈动脉超声检查技术对其中620例患者进行了亚临床动脉粥样硬化评估。在针对潜在混杂因素调整结果后,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,未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。我们的结果未证实RA中ABOrs579459,PPAP2Brs17114036,ADAMTS7rs3825807,PIK3CGrs17398575和EDNRArs1878406与亚临床动脉粥样硬化和CV疾病之间的关联。

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