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美洛昔康与心肌梗死风险:一项基于人群的巢式病例对照研究。

Meloxicam and risk of myocardial infarction: a population-based nested case-control study.

机构信息

Division of Rheumatology, Brown University School of Medicine, Brown University Warren Alpert School of Medicine, 375 Wampanoag Trail, Office 289, E. Providence, RI, 02915, USA.

Section of Rheumatology, Boston University Medical Centre, Boston, MA, USA.

出版信息

Rheumatol Int. 2017 Dec;37(12):2071-2078. doi: 10.1007/s00296-017-3835-x. Epub 2017 Oct 13.

Abstract

Certain non-steroidal anti-inflammatory drugs (NSAIDs) have been associated with an increased risk of myocardial infarction (MI), a risk linked to cyclo-oxygenase-2 inhibition. There are limited studies assessing the risk of MI associated with meloxicam, an increasingly popular drug with COX-2 inhibiting properties. A nested matched case-control study using The Health Improvement Network, a UK population-based database was conducted. NSAID users between 35 and 89 years of age with at least 1 year enrollment in the cohort were included. Incident MI cases were matched on age, sex, practice and event date with up to 4 controls. NSAID exposure was categorized as remote (between 60 days and 1 year), recent (between 1 and 60 days) or current relative to the event date. Current users were further classified as naproxen (negative control), diclofenac (positive control), meloxicam or other NSAID users. Multivariable conditional logistic regression was conducted to determine the risk of MI for each NSAID use categories compared with that of remote users. 9291 MI cases were matched with 30,676 controls. The cases had a higher prevalence of traditional cardiac risk factors, chronic kidney disease and inflammatory arthritis and cardioprotective drug utilization. The adjusted odds ratio of MI for current user compared to remote users were: meloxicam 1.38 (1.17-1.63), naproxen 1.12 (0.96-1.30) and diclofenac 1.37 (1.25-1.50). In this large population-based study, meloxicam increased the risk of MI by 38%. This study warrants cautious use of this increasingly popular drug.

摘要

某些非甾体抗炎药(NSAIDs)与心肌梗死(MI)风险增加有关,这种风险与环氧化酶-2 抑制有关。目前评估美洛昔康(一种具有 COX-2 抑制作用的日益流行的药物)与 MI 相关风险的研究有限。本研究采用英国基于人群的健康改进网络(The Health Improvement Network)开展了一项巢式匹配病例对照研究。纳入年龄在 35 至 89 岁之间、在队列中至少登记 1 年的 NSAID 使用者。MI 病例根据年龄、性别、实践和事件日期与最多 4 名对照进行匹配。根据与事件日期的时间关系,将 NSAID 暴露分为远程(60 天至 1 年)、近期(1 至 60 天)或当前。当前使用者进一步分为萘普生(阴性对照)、双氯芬酸(阳性对照)、美洛昔康或其他 NSAID 使用者。多变量条件逻辑回归用于确定与远程使用者相比,每种 NSAID 使用类别发生 MI 的风险。9291 例 MI 病例与 30676 例对照相匹配。病例组具有更高的传统心脏危险因素、慢性肾脏病和炎症性关节炎以及心脏保护药物使用的患病率。与远程使用者相比,当前使用者发生 MI 的调整后比值比为:美洛昔康 1.38(1.17-1.63)、萘普生 1.12(0.96-1.30)和双氯芬酸 1.37(1.25-1.50)。在这项大型基于人群的研究中,美洛昔康使 MI 的风险增加了 38%。本研究提示在临床实践中应谨慎使用这种日益流行的药物。

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