Hamilton John L, Nagao Masashi, Levine Brett R, Chen Di, Olsen Bjorn R, Im Hee-Jeong
Department of Biochemistry, Rush University Medical Center, Chicago, IL, USA.
Department of Developmental Biology, Harvard School of Dental Medicine, Boston, MA, USA.
J Bone Miner Res. 2016 May;31(5):911-24. doi: 10.1002/jbmr.2828. Epub 2016 Apr 8.
Increased vascular endothelial growth factor (VEGF) levels are associated with osteoarthritis (OA) progression. Indeed, VEGF appears to be involved in OA-specific pathologies including cartilage degeneration, osteophyte formation, subchondral bone cysts and sclerosis, synovitis, and pain. Moreover, a wide range of studies suggest that inhibition of VEGF signaling reduces OA progression. This review highlights both the potential significance of VEGF in OA pathology and pain, as well as potential benefits of inhibition of VEGF and its receptors as an OA treatment. With the emergence of the clinical use of anti-VEGF therapy outside of OA, both as high-dose systemic treatments and low-dose local treatments, these particular therapies are now more widely understood. Currently, there is no established disease-modifying drug available for patients with OA, which warrants continued study of the inhibition of VEGF signaling in OA, as stand-alone or adjuvant therapy. © 2016 American Society for Bone and Mineral Research.
血管内皮生长因子(VEGF)水平升高与骨关节炎(OA)进展相关。事实上,VEGF似乎参与了OA特有的病理过程,包括软骨退变、骨赘形成、软骨下骨囊肿和硬化、滑膜炎以及疼痛。此外,大量研究表明抑制VEGF信号传导可减缓OA进展。本综述强调了VEGF在OA病理和疼痛中的潜在重要性,以及抑制VEGF及其受体作为OA治疗方法的潜在益处。随着抗VEGF疗法在OA以外的临床应用出现,无论是高剂量全身治疗还是低剂量局部治疗,这些特殊疗法现在得到了更广泛的理解。目前,尚无已确立的可用于OA患者的病情缓解药物,这使得继续研究抑制VEGF信号传导作为OA的单独或辅助治疗方法很有必要。© 2016美国骨与矿物质研究学会。