Domżalski Marcin, Migliore Alberto
Department of Orthopaedics and Trauma, Veteran's Memorial Hospital, Medical University of Lodz, Lodz, Poland.
Unit of Rheumatology, S. Pietro Fatebenefratelli Hospital, Via Cassia 600, 00189, Rome, Italy.
Rheumatol Ther. 2022 Aug;9(4):957-974. doi: 10.1007/s40744-022-00450-z. Epub 2022 May 3.
Viscosupplementation by intra-articular (i.a.) injection of the non-sulfated glycosaminoglycan (GAG) hyaluronic acid (HA) is a conservative therapy widely accepted in clinical practice for the management of osteoarthritis (OA) and joint diseases. The aim of viscosupplementation is to restore the rheological properties of the synovial fluid to relieve joint inflammation and pain and improve joint function through a chondroprotective effect. However, there is a range of hyaluronic acid products for OA that differ in preparation, molecular weight, rheological characteristics and concentration, and different i.a. formulations are more suited to particular patient populations and clinical situations, in part because of anatomical differences between joints. This paper focuses on innovative hybrid cooperative complexes of high and low molecular weight hyaluronic acid (HA-HL) and hyaluronic acid plus sodium chondroitin (HA-SC) that have been developed. Both products are formulated with pharmaceutical-grade, highly purified hyaluronic acid obtained with a multi-step biofermentation process, with properties that make them suitable across a range of degenerative joint diseases. They represent progress in building on the symptomatic and functional benefits of viscosupplementation in joint disease, with the additional beneficial effect of treating the patient with a high concentration of GAGs by a low number of injections. Here, we review the clinical evidence for the efficacy of a hybrid cooperative compound of HA-HL in various degenerative joint diseases, which suggests a synergistic effect of the different molecular weight hyaluronans that together more closely mimic the physiological composition of synovial fluid. Similarly, the evidence shows that HA-SC is safe, effective, and well tolerated in hip OA, with rapid and clinically significant improvements in pain symptoms and functionality. Such innovations in viscosupplementation expand the usefulness of the modality in the management of OA and other joint diseases, complemented by a lack of systemic or local side effects that allow the concurrent use of other drugs if needed.
通过关节内(i.a.)注射非硫酸化糖胺聚糖(GAG)透明质酸(HA)进行粘弹性补充是临床实践中广泛接受的用于治疗骨关节炎(OA)和关节疾病的保守疗法。粘弹性补充的目的是恢复滑液的流变学特性,以减轻关节炎症和疼痛,并通过软骨保护作用改善关节功能。然而,有一系列用于OA的透明质酸产品,它们在制剂、分子量、流变学特性和浓度方面存在差异,并且不同的关节内制剂更适合特定的患者群体和临床情况,部分原因是关节之间存在解剖学差异。本文重点介绍已开发的高分子量和低分子量透明质酸(HA-HL)以及透明质酸加硫酸软骨素(HA-SC)的创新混合协同复合物。这两种产品均采用通过多步生物发酵过程获得的药用级、高度纯化的透明质酸配制而成,其特性使其适用于一系列退行性关节疾病。它们在关节疾病中基于粘弹性补充的症状性和功能性益处取得了进展,通过少量注射用高浓度的GAG治疗患者具有额外的有益效果。在此,我们回顾了HA-HL混合协同复合物在各种退行性关节疾病中疗效的临床证据,这表明不同分子量透明质酸的协同作用能更紧密地模拟滑液的生理组成。同样,证据表明HA-SC在髋OA中是安全、有效的,且耐受性良好,疼痛症状和功能有快速且临床上显著的改善。粘弹性补充的此类创新扩大了该方法在OA和其他关节疾病管理中的用途,同时缺乏全身或局部副作用,必要时允许同时使用其他药物。