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迈向骨关节炎精准医学:聚焦滑液蛋白质组学。

Towards Precision Medicine for Osteoarthritis: Focus on the Synovial Fluid Proteome.

机构信息

Orthopaedics Unit, Department of Basic Medical Science, Neuroscience and Sensory Organs, School of Medicine, University of Bari "Aldo Moro", AOU Consorziale Policlinico, 70124 Bari, Italy.

PhD. Course in Public Health, Clinical Medicine and Oncology, University of Bari "Aldo Moro", Piazza Giulio Cesare 11, 70124 Bari, Italy.

出版信息

Int J Mol Sci. 2022 Aug 27;23(17):9731. doi: 10.3390/ijms23179731.

Abstract

Osteoarthritis (OA) is a joint degenerative disease that most affects old age. The study of proteomics in synovial fluid (SF) has the task of providing additional elements to diagnose and predict the progress of OA. This review aims to identify the most significant biomarkers in the study of OA and to stimulate their routine use. Some of the major components of the ECM, such as proteoglycan aggrecan and decorin, were found considerably reduced in OA. Some biomarkers have proved useful for staging the temporality of OA: Periostin was found to be increased in early OA, while CRTA1 and MMPs were found to be increased in late OA. In its natural attempt at tissue regeneration, Collagen III was found to be increased in early OA while decreased in late OA. Some molecules studied in other areas, such as ZHX3 (oncological marker), LYVE1, and VEGF (lymph and angiogenesis markers), also have been found to be altered in OA. It also has been recorded that alteration of the hormonal pathway, using a dosage of PPAR-γ and RETN, can influence the evolution of OA. IL-1, one of the most investigated biomarkers in OA-SF, is not as reliable as a target of OA in recent studies. The study of biomarkers in SF appears to be, in combination with the clinical and radiological aspects, an additional weapon to address the diagnosis and staging of OA. Therefore, it can guide us more appropriately towards the indication of arthroplasty in patients with OA.

摘要

骨关节炎(OA)是一种主要影响老年人群的关节退行性疾病。滑液(SF)中的蛋白质组学研究的任务是提供额外的元素来诊断和预测 OA 的进展。本综述旨在确定 OA 研究中最重要的生物标志物,并促进其常规使用。一些 ECM 的主要成分,如蛋白聚糖聚集素和核心蛋白聚糖,在 OA 中发现明显减少。一些生物标志物已被证明对分期 OA 的时间进程有用:骨桥蛋白在外周 OA 中增加,而 CRTA1 和 MMPs 在晚期 OA 中增加。在其组织再生的自然尝试中,胶原蛋白 III 在早期 OA 中增加,而在晚期 OA 中减少。在其他领域研究的一些分子,如 ZHX3(肿瘤标志物)、LYVE1 和 VEGF(淋巴管和血管生成标志物),也被发现改变了 OA。还记录到,改变激素途径,使用 PPAR-γ 和 RETN 的剂量,可以影响 OA 的演变。IL-1 是 OA-SF 中研究最多的生物标志物之一,但在最近的研究中,它作为 OA 靶点并不那么可靠。SF 中生物标志物的研究似乎与临床和影像学方面相结合,是一种额外的武器,可以解决 OA 的诊断和分期问题。因此,它可以更恰当地指导我们对 OA 患者进行关节置换的指示。

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