Rheumatology and Clinical Immunology, IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089, Rozzano, Milan, Italy.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Clin Rev Allergy Immunol. 2023 Dec;65(3):403-419. doi: 10.1007/s12016-023-08975-z. Epub 2023 Dec 29.
Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by an increased risk of cardiovascular events, due to the complex interplay between traditional and disease-related risk factors. Chronic inflammation and persistent disease activity are the key determinants of this risk, but despite great improvement in the disease management and prognosis, cardiovascular events are still the main cause of morbidity and mortality in RA cohorts. In the last decades, the advent of new biological and targeted-synthetic DMARDs was accompanied by an improvement in disease activity control, but the role of each class of drugs on CVD risk is still a matter a debate. Since their approval for RA treatment, tumor necrosis factor alpha (TNFα) inhibitors have been widely investigated to better understand their effects on cardiovascular outcomes. The hypothesis that the reduction of chronic inflammation with any treatment may reduce the cardiovascular risk has been recently confuted by the direct comparison of TNFα-inhibitors and JAK inhibitors in patients with RA and coexisting risk factors for cardiovascular disease. The aim of this literature review is to add to the available evidence to analyze the relationship between TNFα-inhibitors and CVD risk in patients with RA and also provide some clinical scenarios to better explain the treatment dilemmas. In particular, while data on major cardiovascular events and thromboembolism seem consistent with an inflammation-mediated benefit with TNFα-inhibitors, there remain concerns about the use of this class of bDMARDs in patients with chronic heart failure.
类风湿关节炎(RA)是一种慢性炎症性疾病,由于传统和与疾病相关的危险因素之间的复杂相互作用,其发生心血管事件的风险增加。慢性炎症和持续的疾病活动是这种风险的关键决定因素,但尽管在疾病管理和预后方面取得了很大进展,心血管事件仍然是 RA 患者发病和死亡的主要原因。在过去的几十年中,新型生物和靶向合成 DMARDs 的出现伴随着疾病活动控制的改善,但每种药物类别对 CVD 风险的作用仍然存在争议。自批准用于 RA 治疗以来,肿瘤坏死因子-α(TNFα)抑制剂已被广泛研究,以更好地了解它们对心血管结局的影响。最近,TNFα 抑制剂和 JAK 抑制剂在伴有心血管疾病危险因素的 RA 患者中的直接比较推翻了这样一种假设,即任何治疗方法降低慢性炎症都可能降低心血管风险。本文献综述的目的是在现有证据的基础上进一步分析 TNFα 抑制剂与 RA 患者 CVD 风险之间的关系,并提供一些临床情况来更好地解释治疗困境。特别是,虽然关于主要心血管事件和血栓栓塞的数据似乎与 TNFα 抑制剂的炎症介导益处一致,但仍有人担心在慢性心力衰竭患者中使用此类 bDMARDs。