Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-C.S.I.C., Granada, Spain.
PLoS One. 2012;7(11):e49214. doi: 10.1371/journal.pone.0049214. Epub 2012 Nov 15.
Rheumatoid arthritis (RA) is a chronic inflammatory disease associated with increased cardiovascular (CV) mortality. Since CD40-CD154 binding has direct consequences on inflammation process initiation, we aimed to replicate previous findings related to disease susceptibility in Spanish RA population. Furthermore, as the major complication in RA disease patients is the development of CV events due to accelerated atherosclerosis, and elevated levels of CD40L/CD154 are present in patients with acute myocardial infarction, we assessed the potential association of CD40 and CD154/CD40L gene variants with CV risk in Spanish RA patients.
One thousand five hundred and seventy-five patients fulfilling the 1987 ACR classification criteria for RA and 1600 matched controls were genotyped for the CD40 rs1883832, rs4810485 and rs1535045 and CD154 rs3092952 and rs3092920 gene polymorphisms, using predesigned TaqMan single nucleotide polymorphism genotyping assays. Afterwards, we investigated the influence of CD40-CD154 gene variants in the development of CV events. Also, in a subgroup of 273 patients without history of CV events, we assessed the influence of these polymorphisms in the risk of subclinical atherosclerosis determined by carotid ultrasonography.
Nominally significant differences in the allele frequencies for the rs1883832 CD40 gene polymorphism between RA patients and controls were found (p=0.038). Although we did not observe a significant association of CD40-CD154 gene variants with the development of CV events, an ANCOVA model adjusted for sex, age at the time of the ultrasonography assessment, follow-up time, traditional CV risk factors and anti-cyclic citrullinated peptide antibodies disclosed a significant association (p=0.0047) between CD40 rs1535045 polymorphism and carotid intima media thickness, a surrogate marker of atherosclerosis.
Data from our pilot study indicate a potential association of rs1883832 CD40 gene polymorphism with susceptibility to RA. Also, the CD40 rs1535045 gene variant may influence development of subclinical atherosclerosis in RA patients.
类风湿关节炎(RA)是一种与心血管(CV)死亡率升高相关的慢性炎症性疾病。由于 CD40-CD154 结合对炎症过程的启动有直接影响,我们旨在复制西班牙 RA 人群中与疾病易感性相关的先前发现。此外,由于 RA 疾病患者的主要并发症是由于加速动脉粥样硬化而导致的 CV 事件的发展,并且在急性心肌梗死患者中存在升高的 CD40L/CD154 水平,我们评估了 CD40 和 CD154/CD40L 基因变异与西班牙 RA 患者 CV 风险的潜在关联。
1575 名符合 1987 年 ACR 分类标准的 RA 患者和 1600 名匹配对照者接受 CD40 rs1883832、rs4810485 和 rs1535045 以及 CD154 rs3092952 和 rs3092920 基因多态性的基因分型,使用预先设计的 TaqMan 单核苷酸多态性基因分型检测。之后,我们研究了 CD40-CD154 基因变异在 CV 事件发展中的影响。此外,在 273 名无 CV 事件史的亚组患者中,我们评估了这些多态性在颈动脉超声确定的亚临床动脉粥样硬化风险中的影响。
在 RA 患者和对照组之间,CD40 基因 rs1883832 多态性的等位基因频率存在显著差异(p=0.038)。尽管我们没有观察到 CD40-CD154 基因变异与 CV 事件的发生之间存在显著关联,但调整超声评估时的性别、年龄、随访时间、传统 CV 危险因素和抗环瓜氨酸肽抗体的协方差分析模型显示,CD40 rs1535045 多态性与动脉粥样硬化的替代标志物颈动脉内膜中层厚度之间存在显著关联(p=0.0047)。
我们的初步研究数据表明,CD40 rs1883832 基因多态性可能与 RA 的易感性相关。此外,CD40 rs1535045 基因变异可能影响 RA 患者的亚临床动脉粥样硬化的发展。