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The effects of tumour necrosis factor inhibitors methotrexate non-steroidal anti-inflammatory drugs and corticosteroids on cardiovascular events in rheumatoid arthritis psoriasis and psoriatic arthritis: a systematic review and meta-analysis

机译:肿瘤坏死因子抑制剂甲氨蝶呤非甾体类抗炎药和皮质类固醇对类风湿性关节炎牛皮癣和牛皮癣性关节炎的心血管事件的影响:系统评价和荟萃分析

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摘要

The objective of this systematic literature review was to determine the association between cardiovascular events (CVEs) and antirheumatic drugs in rheumatoid arthritis (RA) and psoriatic arthritis (PsA)/psoriasis (Pso).Systematic searches were performed of MEDLINE, EMBASE and Cochrane databases (1960 to December 2012) and proceedings from major relevant congresses (2010–2012) for controlled studies and randomised trials reporting confirmed CVEs in patients with RA or PsA/Pso treated with antirheumatic drugs. Random-effects meta-analyses were performed on extracted data.Out of 2630 references screened, 34 studies were included: 28 in RA and 6 in PsA/Pso. In RA, a reduced risk of all CVEs was reported with tumour necrosis factor inhibitors (relative risk (RR), 0.70; 95% CI 0.54 to 0.90; p=0.005) and methotrexate (RR, 0.72; 95% CI 0.57 to 0.91; p=0.007). Non-steroidal anti-inflammatory drugs (NSAIDs) increased the risk of all CVEs (RR, 1.18; 95% CI 1.01 to 1.38; p=0.04), which may have been specifically related to the effects of rofecoxib. Corticosteroids increased the risk of all CVEs (RR, 1.47; 95% CI 1.34 to 1.60; p<0.001). In PsA/Pso, systemic therapy decreased the risk of all CVEs (RR, 0.75; 95% CI 0.63 to 0.91; p=0.003).In RA, tumour necrosis factor inhibitors and methotrexate are associated with a decreased risk of all CVEs while corticosteroids and NSAIDs are associated with an increased risk. Targeting inflammation with tumour necrosis factor inhibitors or methotrexate may have positive cardiovascular effects in RA. In PsA/Pso, limited evidence suggests that systemic therapies are associated with a decrease in all CVE risk.
机译:该系统文献综述的目的是确定类风湿关节炎(RA)和银屑病关节炎(PsA)/牛皮癣(Pso)中心血管事件(CVE)与抗风湿药之间的相关性。对MEDLINE,EMBASE和Cochrane数据库进行了系统搜索(1960年至2012年12月)以及主要相关国会会议(2010-2012年)进行的对照研究和随机试验报告,证实接受抗风湿药治疗的RA或PsA / Pso患者中的CVE。对提取的数据进行随机效应荟萃分析。在筛选的2630篇参考文献中,包括34项研究:RA中28项,PsA / Pso中6项。在RA中,据报道,肿瘤坏死因子抑制剂(相对风险(RR),0.70; 95%CI 0.54至0.90; p = 0.005)和甲氨蝶呤(RR,0.72; 95%CI 0.57至0.91;相对危险度(RR)0.70; 95%CI 0.57至0.91)降低了所有CVE的风险。 p = 0.007)。非甾体类抗炎药(NSAIDs)增加了所有CVE的风险(RR,1.18; 95%CI 1.01至1.38; p = 0.04),这可能与罗非昔布的作用有关。皮质类固醇会增加所有CVE的风险(RR,1.47; 95%CI 1.34至1.60; p <0.001)。在PsA / Pso中,全身性治疗降低了所有CVE的风险(RR,0.75; 95%CI 0.63至0.91; p = 0.003)。在RA中,肿瘤坏死因子抑制剂和甲氨蝶呤与所有皮质类固醇的CVE风险均降低有关NSAIDs与增加的风险相关。用肿瘤坏死因子抑制剂或甲氨蝶呤靶向炎症可能在RA中具有积极的心血管作用。在PsA / Pso中,有限的证据表明全身治疗与所有CVE风险的降低有关。

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