Cardiovascular safety of anti-TNF-alpha therapies: Facts and unsettled issues

被引:45
作者
Cacciapaglia, Fabio [1 ,2 ]
Navarini, Luca
Menna, Pierantonio
Salvatorelli, Emanuela
Minotti, Giorgio
Afeltra, Antonella
机构
[1] N Melli Hosp, I-72027 San Pietro Vco, Brindisi, Italy
[2] Campus Biomed Univ, Integrated Res Ctr, Rome, Italy
关键词
TNF-alpha; Heart failure; Anti-TNF-alpha agents; Rheumatoid arthritis; Safety; TUMOR-NECROSIS-FACTOR; RHEUMATOID-ARTHRITIS; HEART-FAILURE; ISCHEMIA/REPERFUSION INJURY; CORONARY MICROEMBOLIZATION; EVENTS; RISK; CARDIOPROTECTION; REDUCTION;
D O I
10.1016/j.autrev.2011.04.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Tumor necrosis factor alpha (TNFa) plays a central role in the pathogenesis of both rheumatoid arthritis (RA) and heart failure (HF). Over the last years RA could benefit from TNFa inhibitors that mitigated disease activity, decreased structural damage, and prevented cardiovascular events. Contraindications to clinical use of TNFa inhibitors may include infections, autoimmune disorders, demyelinating disease, cancer, and heart failure. Overall, these pathological conditions do not appear to increase significantly during treatment with TNFa antagonists compared to placebo. Clinical trials probed these drugs in non RA HF patients produced disappointing results and formed the basis to contraindicate TNFa inhibitors in patients with moderate-severe HF. Although National Registries provide apparently encouraging data about HF safety of anti-TNFa therapies, they cannot adequately assess the actual risk, as these drugs are administered to patients with no cardiac dysfunction. These findings introduced a "rheumatological dilemma" in the clinical management of RA with anti-TNFa. Probably, in RA patients anti-TNFa agents would intercept TNFa and prevent its toxic effects on heart function, while in patients with advanced heart damage (NYHA class HF), anti-TNFa agents would interfere with the beneficial preconditioning effects of TNFa. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:631 / 635
页数:5
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