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骨关节炎、类风湿性关节炎和血友病性关节病的发病机制:血管生成的作用。

Pathogenesis of osteoarthritis, rheumatoid arthritis, and hemophilic arthropathy: The role of angiogenesis.

作者信息

Caliogna Laura, Berni Micaela, Torriani Camilla, Mancuso Maria Elisa, Di Minno Matteo Nicola Dario, Brancato Alice Maria, Jannelli Eugenio, Mosconi Mario, Pasta Gianluigi

机构信息

Orthopedics and Traumatology Clinic, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.

Center for Thrombosis and Hemorrhagic Diseases, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.

出版信息

Haemophilia. 2024 Nov;30(6):1256-1264. doi: 10.1111/hae.15097. Epub 2024 Sep 19.

Abstract

INTRODUCTION

The 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).

AIM

The objective is to try to highlight similarities and differences in the three pathological conditions and understand both molecular and physiological mechanisms.

METHOD

We have carried out a systematic review of the available literature following the guidelines Preferred Reporting Items for Systematic Reviews and Meta-analysis (PRISMA).

RESULTS

By 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.

CONCLUSION

In 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.

摘要

引言

“慢性炎症性关节炎”(IA)一词可用于定义一组异质性疾病,其中滑膜炎症是共同特征,但其发病机制和临床结果各不相同。这种情况可见于骨关节炎(OA)、类风湿关节炎(RA)和血友病性关节病(HA)。

目的

目的是试图突出这三种病理状况的异同,并了解分子和生理机制。

方法

我们按照系统评价和Meta分析的首选报告项目(PRISMA)指南,对现有文献进行了系统评价。

结果

通过比较文献中关于OA、RA和HA的数据,我们发现这三种病理状况在初始病因上有所不同,但它们激发相同的分子途径。

结论

在本综述中,我们突出了这些疾病之间的异同,为未来体内和体外研究开发新的治疗药物创造思路,并提出可能的生物标志物以跟踪疾病的进展和严重程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9000/11659485/b566aad2a856/HAE-30-1256-g004.jpg

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