Hung Yao-Min, Lin Lichi, Chen Chyong-Mei, Chiou Jeng-Yuan, Wang Yu-Hsun, Wang Paul Yung-Pou, Wei James Cheng-Chung
Department of Emergency Medicine, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Institute of Public Health, School of Medicine, National Yang Ming University, Taipei, Taiwan.
PLoS One. 2017 Jun 28;12(6):e0179081. doi: 10.1371/journal.pone.0179081. eCollection 2017.
To determine whether anti-rheumatic drug usage is associated with risk of coronary artery diseases (CAD) in incident Rheumatoid Arthritis (RA) patients.
Data were obtained from the Taiwan National Health Insurance Research Database. The study cohort comprised 6260 patients who were newly diagnosed with RA between 2001-2010. The study endpoint was occurrence of CAD according to the ICD-9-CM codes. We used the WHO Defined Daily Dose (DDD) as a tool to assess the drugs exposure. The Cox proportional hazards regression model was used to estimate the hazard ratio (HR) of disease after controlling for demographic and other co-morbidities. When the proportionality assumption is violated, a spline curve of the Scaled Schoenfeld residuals is fitted to demonstrate the estimated effect on CAD over time for drug usage.
Among RA patients, use of celecoxib, and etoricoxib was associated with significantly decreased incidence of CAD. The adjusted HR(95% CI) of CAD for low-dose celecoxib (DDD≦1) and high-dose user were 0.47(0.34, 0.65) and 0.37(0.24, 0.58) during the 4 year follow-up time; however, it became 0.98(0.70, 1.37) and1.29(0.85, 1.95). Adjusted HR(95% CI) of CAD for etoricoxib users remained 0.47(0.26, 0.84).
This study revealed association of decreased CAD risk in RA patients taking 2 different kinds of COX-2i in comparison with nonusers. The effect might be changed over time, after about 4 years.
确定抗风湿药物的使用是否与初发类风湿关节炎(RA)患者的冠状动脉疾病(CAD)风险相关。
数据来自台湾国民健康保险研究数据库。研究队列包括2001年至2010年间新诊断为RA的6260名患者。研究终点是根据国际疾病分类第九版临床修订本(ICD-9-CM)编码确定的CAD发生情况。我们使用世界卫生组织规定的每日剂量(DDD)作为评估药物暴露的工具。采用Cox比例风险回归模型,在控制人口统计学和其他合并症后估计疾病的风险比(HR)。当比例假设被违反时,拟合标准化Schoenfeld残差的样条曲线,以显示药物使用随时间对CAD的估计影响。
在RA患者中,使用塞来昔布和依托考昔与CAD发病率显著降低相关。在4年随访期间,低剂量塞来昔布(DDD≤1)使用者和高剂量使用者CAD的校正HR(95%CI)分别为0.47(0.34,0.65)和0.37(0.24,0.58);然而,后来分别变为0.98(0.70,1.37)和1.29(0.85,1.95)。依托考昔使用者CAD的校正HR(95%CI)仍为0.47(0.26,0.84)。
本研究显示,与未使用者相比,服用两种不同COX-2抑制剂的RA患者CAD风险降低有关。大约4年后,这种影响可能会随时间变化。