Taylor Peter C, Balsa Alejandro, Mongey Anne-Barbara, Filková Mária, Chebbah Myriam, Le Clanche Solenn, Verhagen Linda A W, Witte Torsten, Opris-Belinski Daniela, Marotte Hubert, Avouac Jérôme
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Windmill Road, Oxford, OX3 7LD, UK.
Rheumatology Unit, University Hospital La Paz, Institute for Health Research-IdiPAZ, Universidad Autonoma de Madrid, 28046, Madrid, Spain.
Rheumatol Ther. 2024 Dec;11(6):1425-1435. doi: 10.1007/s40744-024-00721-x. Epub 2024 Oct 14.
This commentary explores the potential cardiovascular (CV) benefits of combining methotrexate (MTX) and Janus kinase inhibitors (JAKis) in the treatment of rheumatoid arthritis (RA). While European guidelines recommend MTX as first-line treatment, concerns about the CV risks associated with JAKis have emerged. This article reviews the existing literature to assess the role of concomitant MTX in reducing CV risk when used with JAKis. Clinical trials confirm the efficacy of JAKis in combination with MTX in terms of treatment outcomes in RA. However, the number of major adverse cardiovascular events (MACEs) reported is too low to draw conclusions on adverse CV outcomes. Indirect evidence does, however, suggest potential protective effects of MTX on CV outcomes, as several mechanisms may contribute to MTX's cardioprotective effects, including reduced inflammation, adenosine monophosphate-activated protein kinase (AMPK) activation, increased cholesterol efflux, and adenosine accumulation. These mechanisms and the available data may support the case for CV benefits of concomitant MTX when JAKis are used in the treatment of patients with RA, although further research is needed. In particular, the lipid paradox associated with RA highlights the complex relationship between RA treatments (MTX, JAKis, tumor necrosis factor (TNF) inhibitors, and interleukin (IL)-6 receptor inhibitors), inflammation, different lipid profiles, and CV risk. In the absence of contraindications and when MTX is tolerated, this commentary suggests the concomitant use of MTX and JAKis as a preferred option for optimizing CV protection in patients with RA.
本评论探讨了甲氨蝶呤(MTX)与Janus激酶抑制剂(JAKis)联合用于治疗类风湿关节炎(RA)时潜在的心血管(CV)益处。虽然欧洲指南推荐MTX作为一线治疗药物,但人们已开始关注与JAKis相关的CV风险。本文回顾了现有文献,以评估在与JAKis联用时,联用MTX在降低CV风险方面的作用。临床试验证实了JAKis与MTX联合使用在RA治疗效果方面的有效性。然而,报告的主要不良心血管事件(MACEs)数量过少,无法就不良CV结局得出结论。不过,间接证据确实表明MTX对CV结局可能具有保护作用,因为有几种机制可能有助于MTX的心脏保护作用,包括炎症减轻、腺苷单磷酸激活蛋白激酶(AMPK)激活、胆固醇外流增加和腺苷蓄积。这些机制和现有数据可能支持在使用JAKis治疗RA患者时联用MTX具有CV益处的观点,尽管还需要进一步研究。特别是,与RA相关的脂质悖论凸显了RA治疗(MTX、JAKis、肿瘤坏死因子(TNF)抑制剂和白细胞介素(IL)-6受体抑制剂)、炎症、不同脂质谱和CV风险之间的复杂关系。在没有禁忌证且MTX可耐受的情况下,本评论建议联用MTX和JAKis作为优化RA患者CV保护的首选方案。