Swansea University Medical School, Data Science, Swansea University, Swansea, United Kingdom.
Swansea University Medical School, Data Science, Swansea University, Swansea, United Kingdom.
Semin Arthritis Rheum. 2018 Dec;48(3):367-373. doi: 10.1016/j.semarthrit.2018.03.005. Epub 2018 Mar 17.
Increased cardiovascular risk in rheumatoid arthritis (RA) is well established. Examining traditional cardiovascular risk factors alone underestimates cardiovascular risk in RA. Systematic inflammation, measured by erythrocyte sedimentation rate or C-reactive protein is also a major risk factor. However, the contribution of traditional cardiovascular risk factors (such as obesity and hyperlipidaemia) compared to inflammation is uncertain in psoriatic arthritis (PsA) and RA. We examine the incidence of major adverse cardiac events (MACE) among patients with RA, PsA psoriasis, and controls adjusting for risk factors, inflammation and disease modifying anti-rheumatic drug treatment, to better define cardiovascular risk.
Using the Secure Anonymised Information Linkage databank, comprising routinely collected Welsh health data from 1999 to 2013, the incidence and first occurrence of a MACE in individuals with RA (n = 8650), PsA (n = 2128) and psoriasis (n = 24,630) compared to controls (n = 11,87,706) was investigated.
Traditional cardiovascular risk factors are higher in RA, PsA and psoriasis than controls. After adjusting for these factors, additional cardiovascular risk was only significantly increased in female RA patients (HR = 1.3; 95% CI: 1.0-1.7; p = 0.05) and psoriasis (HR = 1.2; 95% CI: 1.0-1.4; p = 0.02) but not statistically significant for PsA (HR = 1.5; 95% CI: 0.9-2.5; p = 0.13). ESR and CRP were increased in patients with RA but not in patients with psoriasis.
Additional increased cardiovascular risk was observed in female RA and psoriasis but not PsA. Systematic inflammation is higher in RA but not psoriasis, indicating that there are varying mediators of cardiovascular risk across these conditions.
类风湿关节炎(RA)患者的心血管风险增加已得到充分证实。仅检查传统心血管危险因素会低估 RA 患者的心血管风险。红细胞沉降率或 C 反应蛋白等系统性炎症也是一个主要危险因素。然而,在银屑病关节炎(PsA)和 RA 中,传统心血管危险因素(如肥胖和高脂血症)与炎症相比,对心血管风险的贡献尚不确定。我们通过使用 Secure Anonymised Information Linkage 数据库(包含来自 1999 年至 2013 年的威尔士常规健康数据),来检查 RA(n = 8650)、PsA(n = 2128)和银屑病(n = 24630)患者与对照组(n = 1187706)相比,主要不良心脏事件(MACE)的发生率和首次发生情况,以更好地定义心血管风险。
使用 Secure Anonymised Information Linkage 数据库(包含来自 1999 年至 2013 年的威尔士常规健康数据),来检查 RA(n = 8650)、PsA(n = 2128)和银屑病(n = 24630)患者与对照组(n = 1187706)相比,主要不良心脏事件(MACE)的发生率和首次发生情况,以更好地定义心血管风险。
RA、PsA 和银屑病患者的传统心血管危险因素高于对照组。在调整这些因素后,仅女性 RA 患者(HR = 1.3;95%CI:1.0-1.7;p = 0.05)和银屑病患者(HR = 1.2;95%CI:1.0-1.4;p = 0.02)的心血管风险显著增加,但 PsA 患者的心血管风险增加无统计学意义(HR = 1.5;95%CI:0.9-2.5;p = 0.13)。RA 患者的 ESR 和 CRP 升高,但银屑病患者的 ESR 和 CRP 未升高。
女性 RA 和银屑病患者的心血管风险增加,但 PsA 患者则无此现象。RA 患者的系统性炎症较高,但银屑病患者的系统性炎症则较低,这表明这些疾病的心血管风险存在不同的介导因素。