Laura Caliogna, Micaela Berni, Camilla Torriani, Maria Elisa Mancuso, Matteo Nicola Dario Di Minno, Alice Maria Brancato, Eugenio Jannelli, Mario Mosconi, Gianluigi Pasta
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引用次数: 0
摘要
导言 "慢性炎症性关节炎"(IA)一词可用于定义一组异质性疾病,这些疾病的共同特征是滑膜炎症,但发病机制和临床结果各不相同。目的试图强调这三种病理状况的异同,并了解分子和生理机制。方法我们按照系统综述和元分析首选报告项目(PRISMA)指南对现有文献进行了系统综述。结果通过比较有关 OA、RA 和 HA 的文献数据,我们发现这三种病症的最初病因不同,但它们的分子途径相同。结论在这篇综述中,我们强调了这些疾病之间的异同,为今后的体内和体外研究提供了思路,以开发新的治疗药物,并为跟踪疾病的演变和严重程度提出了可能的生物标志物。
Pathogenesis of osteoarthritis, rheumatoid arthritis, and hemophilic arthropathy: The role of angiogenesis
IntroductionThe term ‘chronic inflammatory arthritis’ (IA) can be used to define a group of heterogeneous diseases in which inflammation of the synovium is the common feature while having different pathogenesis and clinical outcomes. This condition can be found in osteoarthritis (OA), rheumatoid arthritis (RA), and hemophilic arthropathy (HA).AimThe objective is to try to highlight similarities and differences in the three pathological conditions and understand both molecular and physiological mechanisms.MethodWe have carried out a systematic review of the available literature following the guidelines Preferred Reporting Items for Systematic Reviews and Meta‐analysis (PRISMA).ResultsBy comparing the data in the literature on OA, RA, and HA we have shown that the three pathologies differ in initial etiology but they motivate the same molecular pathways.ConclusionIn this review we highlighted the similarities and differences between these diseases, creating ideas for future studies both in vivo and in vitro to develop new therapeutic agents and suggest possible biomarkers to follow the evolution and severity of the disease.
期刊介绍:
Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include:
clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI
replacement therapy for clotting factor deficiencies
component therapy in the developing world
transfusion transmitted disease
haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics
nursing
laboratory diagnosis
carrier detection
psycho-social concerns
economic issues
audit
inherited platelet disorders.