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本文引用的文献

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Infectious causes of death in patients with rheumatoid arthritis: an autopsy study.类风湿关节炎患者的感染性死亡原因:一项尸检研究。
Scand J Rheumatol. 2006 Jul-Aug;35(4):273-6. doi: 10.1080/03009740600556258.
2
Anti-TNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies: systematic review and meta-analysis of rare harmful effects in randomized controlled trials.类风湿关节炎中抗 TNF 抗体治疗与严重感染及恶性肿瘤风险:随机对照试验中罕见有害效应的系统评价和荟萃分析
JAMA. 2006 May 17;295(19):2275-85. doi: 10.1001/jama.295.19.2275.
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Relationship between C-reactive protein and subclinical atherosclerosis: the Dallas Heart Study.C反应蛋白与亚临床动脉粥样硬化的关系:达拉斯心脏研究
Circulation. 2006 Jan 3;113(1):38-43. doi: 10.1161/CIRCULATIONAHA.105.575241. Epub 2005 Dec 27.
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Rheumatoid arthritis registries in Sweden.瑞典的类风湿性关节炎登记处。
Clin Exp Rheumatol. 2005 Sep-Oct;23(5 Suppl 39):S195-200.
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Effectiveness of recommendations to prevent reactivation of latent tuberculosis infection in patients treated with tumor necrosis factor antagonists.肿瘤坏死因子拮抗剂治疗患者中预防潜伏性结核感染再激活的建议的有效性
Arthritis Rheum. 2005 Jun;52(6):1766-72. doi: 10.1002/art.21043.
6
Cardiovascular admissions and mortality in an inception cohort of patients with rheumatoid arthritis with onset in the 1980s and 1990s.20世纪80年代和90年代发病的类风湿关节炎初发队列患者的心血管疾病入院率和死亡率。
Ann Rheum Dis. 2005 Nov;64(11):1595-601. doi: 10.1136/ard.2004.034777. Epub 2005 Apr 20.
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Risks of solid cancers in patients with rheumatoid arthritis and after treatment with tumour necrosis factor antagonists.类风湿关节炎患者及使用肿瘤坏死因子拮抗剂治疗后的实体癌风险。
Ann Rheum Dis. 2005 Oct;64(10):1421-6. doi: 10.1136/ard.2004.033993. Epub 2005 Apr 13.
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Cardiovascular death in rheumatoid arthritis: a population-based study.类风湿关节炎患者的心血管死亡:一项基于人群的研究。
Arthritis Rheum. 2005 Mar;52(3):722-32. doi: 10.1002/art.20878.
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Declines in mortality from acute myocardial infarction in successive incidence and birth cohorts of patients with rheumatoid arthritis.类风湿关节炎患者连续发病队列和出生队列中急性心肌梗死死亡率的下降情况。
Circulation. 2004 Sep 28;110(13):1774-9. doi: 10.1161/01.CIR.0000142864.83780.81. Epub 2004 Sep 20.
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Rheumatoid arthritis and accelerated atherogenesis.
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使用肿瘤坏死因子拮抗剂治疗类风湿关节炎时,全因死亡率和特定病因死亡率并不高于预期。

All-cause and cause-specific mortality in rheumatoid arthritis are not greater than expected when treated with tumour necrosis factor antagonists.

作者信息

Carmona Loreto, Descalzo Miguel Angel, Perez-Pampin Eva, Ruiz-Montesinos Dolores, Erra Alba, Cobo Tatiana, Gómez-Reino Juan J

机构信息

Research Unit, Spanish Foundation of Rheumatology, Madrid, Spain.

出版信息

Ann Rheum Dis. 2007 Jul;66(7):880-5. doi: 10.1136/ard.2006.067660. Epub 2007 Feb 26.

DOI:10.1136/ard.2006.067660
PMID:17324968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1955107/
Abstract

BACKGROUND

Mortality is increased in rheumatoid arthritis (RA), mainly because of cardiovascular (CV) events, cancer and infections. Recent data suggest that treatment with tumour necrosis factor (TNF) antagonists may affect this trend.

OBJECTIVE

To assess whether treatment with TNF antagonists is associated with reduction in CV events, cancer and infection rates, and in mortality in patients with RA treated and not treated with TNF antagonists.

METHODS

BIOBADASER is a registry for active long-term follow-up of safety of biological treatments in patients with RA. It includes 4459 patients with RA treated with TNF antagonists. EMECAR is an external RA cohort (n = 789) established to define the characteristics of the disease in Spain and to assess comorbidity. The incidence density (ischaemic heart disease) of CV events, cancer and infections was estimated and compared. The standardised mortality ratio was compared with the rate in the general population. A propensity score was used to match cohorts by the probability of being treated.

RESULTS

Rates of CV and cancer events are significantly higher in EMECAR than in BIOBADASER (RR 5-7 for different CV events, and RR 2.9 for cancer), whereas the rate of serious infections is significantly higher in BIOBADASER (RR 1.6). Mortality ratio of BIOBADASER by EMECAR is 0.32 (0.20-0.53) for all causes of death, 0.58 (0.24-1.41) for CV events, 0.52 (0.21-1.29) for infection and 0.36 (0.10-1.30) for cancer-related deaths.

CONCLUSION

Morbidity, other than infection, and mortality are not higher than expected in patients with RA treated with TNF antagonists.

摘要

背景

类风湿关节炎(RA)患者的死亡率增加,主要原因是心血管(CV)事件、癌症和感染。近期数据表明,使用肿瘤坏死因子(TNF)拮抗剂进行治疗可能会影响这一趋势。

目的

评估使用TNF拮抗剂治疗是否与RA患者(无论是否接受TNF拮抗剂治疗)的CV事件、癌症和感染率降低以及死亡率降低相关。

方法

BIOBADASER是一个对RA患者生物治疗安全性进行长期主动随访的登记系统。它纳入了4459例接受TNF拮抗剂治疗的RA患者。EMECAR是一个外部RA队列(n = 789),其建立目的是确定西班牙该疾病的特征并评估合并症。对CV事件、癌症和感染的发病密度(缺血性心脏病)进行了估计和比较。将标准化死亡率与普通人群的死亡率进行了比较。使用倾向评分通过治疗概率对队列进行匹配。

结果

EMECAR中CV和癌症事件的发生率显著高于BIOBADASER(不同CV事件的相对风险为5 - 7,癌症的相对风险为2.9),而BIOBADASER中严重感染的发生率显著更高(相对风险为1.6)。BIOBADASER相对于EMECAR的全因死亡率为0.32(0.20 - 0.53),CV事件为0.58(0.24 - 1.41),感染为0.52(0.21 - 1.29),癌症相关死亡为方法:BIOBADASER是一个对RA患者生物治疗安全性进行长期主动随访的登记系统。它纳入了4459例接受TNF拮抗剂治疗的RA患者。EMECAR是一个外部RA队列(n = 789),其建立目的是确定西班牙该疾病的特征并评估合并症。对CV事件、癌症和感染的发病密度(缺血性心脏病)进行了估计和比较。将标准化死亡率与普通人群的死亡率进行了比较。使用倾向评分通过治疗概率对队列进行匹配。

结果

EMECAR中CV和癌症事件的发生率显著高于BIOBADASER(不同CV事件的相对风险为5 - 7,癌症的相对风险为2.9),而BIOBADASER中严重感染的发生率显著更高(相对风险为1.6)。BIOBADASER相对于EMECAR的全因死亡率为0.32(0.20 - 0.53),CV事件为0.58(0.24 - 1.41),感染为0.52(0.21 - 1.29),癌症相关死亡为0.36(0.10 - 1.30)。

结论

除感染外,接受TNF拮抗剂治疗的RA患者的发病率和死亡率并不高于预期。 0.36(0.10 - 1.30)。

结论

除感染外,接受TNF拮抗剂治疗的RA患者的发病率和死亡率并不高于预期。