Methotrexate Intolerance in Juvenile Idiopathic Arthritis: Definition, Risks, and Management.

IF 3.4 3区 医学 Q1 PEDIATRICS
Pediatric Drugs Pub Date : 2024-09-01 Epub Date: 2024-07-24 DOI:10.1007/s40272-024-00643-9
Camilla Wibrand, Nini Kyvsgaard, Troels Herlin, Mia Glerup
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引用次数: 0

Abstract

Juvenile idiopathic arthritis is the most common rheumatic disorder in childhood and adolescence posing a significant threat of short-term and long-term disability if left untreated. Methotrexate is a folic acid analog with various immunomodulatory properties. It has demonstrated significant efficacy for the treatment of juvenile idiopathic arthritis, often considered the preferred first-line disease-modifying anti-rheumatic drug given as monotherapy or in combination with biological drugs. Despite this, there is a considerable risk for treatment disruptions owing to the high prevalence of methotrexate intolerance, with symptoms such as nausea, stomach ache, vomiting, and behavioral symptoms. Many different risk factors for the intolerance have been proposed including gender, age, disease activity, treatment duration, dosing and administration, and genetic and psychological factors. As the studies have shown contradictory results, many questions are left unanswered. Therefore, a consensus regarding outcome measures and reporting is crucial. In this review, we describe the identification and assessment of methotrexate intolerance and evaluate potential risk factors, genetic associations as well as management strategies.

青少年特发性关节炎的甲氨蝶呤不耐受:定义、风险和管理。
幼年特发性关节炎是儿童和青少年时期最常见的风湿性疾病,如果不及时治疗,会造成严重的短期和长期残疾。甲氨蝶呤是一种叶酸类似物,具有多种免疫调节特性。它在治疗幼年特发性关节炎方面疗效显著,通常被认为是单药治疗或与生物药物联合使用的首选一线改变病情抗风湿药物。尽管如此,由于甲氨蝶呤不耐受的发生率很高,出现恶心、胃痛、呕吐和行为症状等症状,因此治疗中断的风险相当大。不耐受的风险因素有很多种,包括性别、年龄、疾病活动性、治疗时间、剂量和给药方式,以及遗传和心理因素。由于研究结果相互矛盾,许多问题仍未得到解答。因此,就结果测量和报告达成共识至关重要。在这篇综述中,我们介绍了甲氨蝶呤不耐受的识别和评估,并评估了潜在的风险因素、遗传关联以及管理策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Drugs
Pediatric Drugs PEDIATRICS-PHARMACOLOGY & PHARMACY
CiteScore
7.20
自引率
0.00%
发文量
54
审稿时长
>12 weeks
期刊介绍: Pediatric Drugs promotes the optimization and advancement of all aspects of pharmacotherapy for healthcare professionals interested in pediatric drug therapy (including vaccines). The program of review and original research articles provides healthcare decision makers with clinically applicable knowledge on issues relevant to drug therapy in all areas of neonatology and the care of children and adolescents. The Journal includes: -overviews of contentious or emerging issues. -comprehensive narrative reviews of topics relating to the effective and safe management of drug therapy through all stages of pediatric development. -practical reviews covering optimum drug management of specific clinical situations. -systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. -Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in the pediatric population. -original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Pediatric Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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