甲托雷克萨特治疗青少年异常性关节炎
Joachim Tan1,2, William D Renton2,3,4, Samuel L Whittle2,5
1Department of Rheumatology, Children's Health Queensland, South Brisbane, Australia.
The Cochrane database of systematic reviews
|February 9, 2024
概括
甲托雷克萨特可以改善青少年异常性关节炎 (JIA) 的治疗反应,但对疼痛的影响很小. 严重的不良事件很少发生,支持其作为疾病修饰性抗风湿药物 (DMARD) 在JIA管理中的使用.
科学领域:
- 儿科风湿病学 儿科风湿病学
- 药理学 药理学是指药理学的学科.
- 临床试验 临床试验
背景情况:
- 青少年异常性关节炎 (JIA) 是童年最常见的类风湿性疾病.
- 甲甲酸是一种广泛使用的疾病修饰性抗风湿药物 (DMARD),具有广泛的免疫调节作用.
- 这次审查是2001年科克莱恩审查的更新,支持JIA的指导方针.
研究的目的:
- 评估在被诊断患有JIA的儿童和青少年中甲铁酸的益处和危害.
- 综合来自随机对照试验 (RCT) 关于甲状腺素的疗效和安全性的证据.
- 为临床实践和JIA治疗指南的制定提供信息.
主要方法:
- 在多个数据库 (CENTRAL,MEDLINE,Embase,试验注册) 进行系统搜索,截至2023年2月1日.
- 包括将甲状腺素与安慰剂,无治疗或其他儿童JIA患者的DMARDs进行比较的RCT.
- 评估结果,包括治疗反应,疾病活性,功能,疼痛,不良事件和戒断,使用GRADE标准.
主要成果:
- 包括五个RCT (575名参与者). 甲甲酸与安慰剂相比,可能会增加治疗反应 (低确定性证据),但对疼痛或幸福感的影响很小.
- 甲托雷克萨特加上关节内葡萄糖皮质类药物治疗对原关节性JIA持续不活性的疾病几乎没有影响.
- 甲托雷克萨特与莱夫卢诺米德对治疗反应或功能的影响很小,对所有结果的证据确定性低.
结论:
- 与安慰剂相比,甲托雷克萨特可能会增强JIA的治疗反应,但对疼痛和幸福感的影响很小.
- 证据表明,当甲状腺素与关节内葡萄皮质类药物结合用于关节性JIA时,甲状腺素的额外益处有限.
- 甲基似乎是一个安全的选择,罕见的严重不良事件,支持其在JIA管理中的作用.
相关概念视频
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents
164
Crohn's disease is an inflammatory bowel disorder marked by chronic inflammation of the GI tract. Various treatment strategies for Crohn's disease are employed, such as immunomodulatory agents, glucocorticoids, and biologics or anti-TNF therapy. Azathioprine (Imuran), a commonly used immunomodulatory drug for Crohn's disease, is converted in the body to mercaptopurine, which inhibits purine biosynthesis and cell proliferation. Both are utilized in severe cases of Inflammatory Bowel...
164
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF
137
Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab...
137
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids
119
Glucocorticoids, a class of anti-inflammatory drugs, are pivotal in treating moderate to severe Crohn's disease by inducing remission. They exhibit their anti-inflammatory action by inhibiting the production of inflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1, and chemokines like IL-8. In addition, they reduce the expression of inflammatory cell adhesion molecules and inhibit gene transcription of nitric oxide synthase, phospholipase A2, cyclooxygenase-2...
119
Inflammatory Bowel Disease IV: Pharmacological Management
127
Upon diagnosis, managing Inflammatory Bowel Disease (IBD) involves addressing several crucial aspects. The primary goals include resting the bowel, correcting malnutrition, and providing symptomatic relief. Resting the bowel may consist of medications to reduce inflammation and promote healing. Correcting malnutrition is essential, often requiring dietary adjustments and nutritional supplements. Symptomatic relief aims to ease pain, diarrhea, and other discomforts in IBD.
Pharmacologic...
Pharmacologic...
127
Drugs for Treatment of Ulcerative Colitis in IBD
141
Ulcerative colitis is a chronic inflammatory condition primarily affecting the colon and rectum. The primary drugs used in the treatment of ulcerative colitis are aminosalicylates. They exhibit anti-inflammatory and immunosuppressive properties. They modulate inflammatory mediators and inhibit the activity of nuclear factor κB (NF-κB). Aminosalicylates also reduce inflammation by inhibiting prostaglandin and leukotriene production and decreasing neutrophil chemotaxis and superoxide...
141
T Cell Types and Functions
1.0K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
1.0K


