Bhosale Uma A, Quraishi Nilofar, Yegnanarayan Radha, Devasthale Dileep
Department of Pharmacology, Smt. Kashibai Navale Medical College and General Hospital, Narhe, Pune, Maharashtra, India.
Department of Orthopedics, Smt. Kashibai Navale Medical College and General Hospital, Narhe, Pune, Maharashtra, India.
Niger Med J. 2014 Sep;55(5):417-22. doi: 10.4103/0300-1652.140386.
Cyclooxygenase-2 inhibitors (COX-2-Is) have recently been concerned in the occurrence of adverse cardiovascular (CV) events. Rofecoxib and valdecoxib has been withdrawn from the market, but celecoxib, etoricoxib and parecoxib continues to be used. Other nonsteroidal anti-inflammatory drugs (NSAIDs) may also increase the risk of CV events. However, clinical trial databases for COX-2-Is had created lots of controversies regarding cardiovascular safety of selective and nonselective cyclooxygenase inhibitors (COX-Is). This study was, conducted to assess and compare the CV risk of COX-Is in arthritic patients over a period of time.
In this prospective cohort study adult arthritics of either sex those were freshly diagnosed or taking COX-Is for < 3 months; were included. Patients were grouped into nonselective and selective COX-2-I groups with reference to treatment they received. The CV risk factors like blood pressure (BP), blood sugar level (BSL), lipid profile, body mass index (BMI) were assessed and compared; demography of CV risk factors was also studied. Data obtained was analysed using Student's 't'-test of OpenEpi statistical software.
Study clearly revealed that all NSAIDs exhibit variable CV risk; however, selective COX-2-Is found to exhibit more CV risk. BMI, BP and lipid profile; the potential CV risk factors, showed significant impairment in selective COX-2-Is group; P < 0.01, P < 0.001 and P < 0.05, respectively, compared to baseline and P < 0.05 vs. nonselective COX-Is for BMI.
This study portrays the potential CV risk of selective COX-2-Is; confirms and re-evaluate the results of earlier studies in this regard.
环氧化酶-2抑制剂(COX-2-Is)最近受到了心血管不良事件发生情况的关注。罗非昔布和伐地昔布已退出市场,但塞来昔布、依托考昔和帕瑞昔布仍在使用。其他非甾体抗炎药(NSAIDs)也可能增加心血管事件的风险。然而,COX-2-Is的临床试验数据库在选择性和非选择性环氧化酶抑制剂(COX-Is)的心血管安全性方面引发了诸多争议。本研究旨在评估和比较一段时间内关节炎患者中COX-Is的心血管风险。
在这项前瞻性队列研究中,纳入了新诊断或服用COX-Is不足3个月的成年关节炎患者,不分性别。根据患者接受的治疗,将其分为非选择性和选择性COX-2-I组。评估并比较了血压(BP)、血糖水平(BSL)、血脂谱、体重指数(BMI)等心血管危险因素;还研究了心血管危险因素的人口统计学特征。使用OpenEpi统计软件的学生t检验对获得的数据进行分析。
研究清楚地表明,所有NSAIDs都表现出不同的心血管风险;然而,发现选择性COX-2-Is表现出更高的心血管风险。BMI、BP和血脂谱这些潜在的心血管危险因素在选择性COX-2-I组中显示出显著损害;与基线相比,P分别<0.01、<0.001和<0.05,与非选择性COX-Is相比,BMI的P<0.05。
本研究描绘了选择性COX-2-Is的潜在心血管风险;证实并重新评估了这方面早期研究的结果。