Efficacy and safety of ibuprofen and naproxen in the treatment of oligoarticular juvenile idiopathic arthritis: bi-national cohort study.

IF 2.9 4区 医学 Q3 IMMUNOLOGY Immunopharmacology and Immunotoxicology Pub Date : 2025-01-09 DOI:10.1080/08923973.2024.2421523
Orly Ohana, Itay Marmor, Rina Ferguson, Yoel Levinsky, Shiri Rubin, Kevin Baszis, Rotem Tal, Liora Harel, Orit Peled, Gil Amarilyo
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Abstract

Objectives: Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children. Nonsteroidal anti-inflammatory drugs (NSAIDs) and intra-articular corticosteroid injections are first-line therapy for oligoarticular JIA. NSAIDs Adverse events (AEs) include gastrointestinal ulcers/bleeding and impaired renal function. The most prescribed NSAIDs for oligoarticular JIA are ibuprofen and naproxen. However, direct comparison between these drugs is lacking. We aimed to compare the efficacy and safety of ibuprofen versus naproxen for oligoarticular JIA.

Methods: This is a bi-national retrospective study of oligoarticular JIA patients treated with either ibuprofen or naproxen as first-line therapy. Efficacy was defined as patients that achieved complete response (no evidence for arthritis). Safety was assessed by the occurrence of adverse events during follow-up.

Results: Of 164 patients, 103 were treated in the Israeli group and 61 in the US group. The study population had a mean age of 4.49 ± 3.55 years, with F:M ratio of ∼2.5:1. No significant difference was found in drug efficacy [Complete response was observed in 15% of the ibuprofen group vs. 17.3% in naproxen group (p = 0.7)]. Treatment duration > 28 days was associated with significantly higher odds for complete response (p = 0.021). For safety, 12 AEs were associated with naproxen, whereas no AEs were associated with ibuprofen (p = 0.004). Treatment was discontinued in all AEs cases.

Conclusions: Ibuprofen and naproxen showed similar albeit low efficacy which emphasizes their role as bridging therapy until IACI is achieved. However, ibuprofen showed better safety profile naproxen and therefore should be considered as first-line therapy.

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布洛芬和萘普生治疗青少年少关节特发性关节炎的疗效和安全性:两国队列研究。
目的:青少年特发性关节炎(JIA)是儿童最常见的风湿性疾病。非甾体抗炎药(NSAIDs)和关节内皮质类固醇注射是治疗寡关节性JIA的一线治疗方法。不良事件(ae)包括胃肠道溃疡/出血和肾功能受损。对于寡关节JIA,最常用的非甾体抗炎药是布洛芬和萘普生。然而,这些药物之间缺乏直接的比较。我们的目的是比较布洛芬和萘普生治疗寡关节性JIA的疗效和安全性。方法:这是一项双国回顾性研究,以布洛芬或萘普生作为一线治疗的寡关节JIA患者。疗效定义为患者达到完全缓解(无关节炎证据)。通过随访期间不良事件的发生来评估安全性。结果:164例患者中,以色列组103例,美国组61例。研究人群的平均年龄为4.49±3.55岁,F:M比为~ 2.5:1。两组疗效差异无统计学意义[布洛芬组完全缓解率为15%,萘普生组为17.3% (p = 0.7)]。治疗持续时间bbb28天与完全缓解的几率显著升高相关(p = 0.021)。安全性方面,萘普生组有12例ae,而布洛芬组无ae (p = 0.004)。所有不良反应病例均停止治疗。结论:布洛芬和萘普生的疗效相似,但较低,强调两者在达到IACI之前的桥接治疗作用。然而,布洛芬表现出更好的安全性,因此应考虑作为一线治疗。
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来源期刊
CiteScore
5.40
自引率
0.00%
发文量
133
审稿时长
4-8 weeks
期刊介绍: The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal. The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome. With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more. Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).
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