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随机、双盲比较关节内多核苷酸和透明质酸固定复方制剂与单独使用透明质酸治疗膝骨关节炎:两年随访。

Randomised, double-blind comparison of a fixed co-formulation of intra-articular polynucleotides and hyaluronic acid versus hyaluronic acid alone in the treatment of knee osteoarthritis: two-year follow-up.

机构信息

Reconstructive Orthopaedic Surgery and Innovative Techniques - Musculoskeletal Tissue Bank, IRCCS Istituto Ortopedico Rizzoli, Via G.C. Pupilli 1, 40136, Bologna, Italy.

Surgical Sciences and Technologies Complex Structure, IRCCS Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136, Bologna, Italy.

出版信息

BMC Musculoskelet Disord. 2021 Sep 12;22(1):773. doi: 10.1186/s12891-021-04648-0.

Abstract

BACKGROUND

A first-year interim analysis of this two-year study suggested that intra-articular injections of highly purified, natural-origin polynucleotides and hyaluronic acid (HA) as a fixed combination (PNHA) might improve knee function and joint pain more effectively than HA alone in patients with knee osteoarthritis (OA). The purpose of the second-year analysis herein described was to verify whether the first-year interim outcomes persist over the whole two-year period.

METHODS

Randomised, double-blind, HA-controlled clinical trial in 100 knee OA patients (98 randomised, 79 completing the study) in a high-specialisation tertiary care setting. The hypothesised difference of efficacy between PNHA and HA for the original sample size estimate is 20%. Treatment cycle: three intra-articular knee injections of either PNHA or HA, at baseline and weekly for two weeks.

EVALUATIONS

Western Ontario and McMaster Universities (WOMAC) score and Knee Society Score (KSS) as, respectively, primary and secondary endpoints, evaluated at baseline and after 2, 6, 12, and 24 months; synovial fluid levels of mediators (at baseline and the end of the treatment cycle). Adverse effects investigated at each control visit.

STATISTICAL ANALYSIS

Kruskal-Wallis test for independent samples (nonparametric one-way analysis of variance) after correction of means for age, Body Mass Index and Kellgren-Lawrence grade. If significant, pairwise post-hoc Sidak multiple comparisons.

RESULTS

KSS total score and KSS pain item: significant improvement in both groups, with significantly more pain improvement in patients treated with PNHA (2-point reduction) than HA (1-point reduction). Both groups experienced significant long-term reductions in WOMAC total scores: significantly stronger in PNHA-treated patients after 24 months with a steady difference of 16% favouring PNHA in WOMAC pain subscore. No clinically significant adverse events in either group.

CONCLUSIONS

The outcomes of the 2-year study confirmed that a short cycle of intra-articular treatment (3 weekly double-blind injections) with polynucleotides (long-acting viscosupplementation properties, chondrocyte activation, pain-relieving properties) in fixed combination with high molecular weight hyaluronic acid is more effective in improving knee function and pain in knee OA patients than HA alone. PNHA may be elective for viscosupplementation in knee OA patients with fastidious and resistant pain and worsening disease.

TRIAL REGISTRATION

NCT02417610 . Registration, 15/04/2015. ClinicalTrials.gov database link.

摘要

背景

对这项为期两年的研究进行的第一年中期分析表明,与单独使用透明质酸(HA)相比,关节内注射高纯度天然来源多核苷酸和 HA 的固定组合(PNHA)可能更有效地改善膝关节骨关节炎(OA)患者的膝关节功能和关节疼痛。本文描述的第二年分析的目的是验证第一年的中期结果是否在整个两年期间持续。

方法

在一家高专科治疗中心,对 100 名膝关节 OA 患者(98 名随机分组,79 名完成研究)进行随机、双盲、HA 对照临床试验。最初样本量估计的假设疗效差异为 20%。治疗周期:在基线和两周内每周进行三次关节内膝关节注射,分别为 PNHA 或 HA。

评估

使用 Western Ontario 和 McMaster 大学(WOMAC)评分和膝关节协会评分(KSS)作为主要和次要终点,分别在基线和 2、6、12 和 24 个月后进行评估;在基线和治疗周期结束时评估滑液中介质的水平。在每次对照就诊时检查不良反应。

统计分析

使用 Kruskal-Wallis 检验进行独立样本(非参数单向方差分析),校正年龄、体重指数和 Kellgren-Lawrence 分级后的均值。如果有显著差异,则进行事后 Sidak 多重比较。

结果

KSS 总分和 KSS 疼痛项目:两组均有显著改善,PNHA 治疗组疼痛改善更显著(减少 2 分),HA 治疗组疼痛改善更显著(减少 1 分)。两组患者的 WOMAC 总分均有显著的长期降低:PNHA 治疗组在 24 个月后降低幅度更强,WOMAC 疼痛子量表中持续 16%的优势有利于 PNHA。两组均无明显临床不良事件。

结论

为期两年的研究结果证实,关节内治疗的短周期(3 周双盲注射)用多核苷酸(长效粘性补充剂特性、软骨细胞激活、止痛特性)与高分子量透明质酸固定结合,对改善膝关节功能和膝关节骨关节炎患者的疼痛比单独使用透明质酸更有效。PNHA 可能是治疗对疼痛敏感且有抵抗力、病情恶化的膝关节骨关节炎患者的首选粘性补充剂。

试验注册

NCT02417610。注册,2015 年 4 月 15 日。ClinicalTrials.gov 数据库链接。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ea8/8436495/74ece758dfb1/12891_2021_4648_Fig1_HTML.jpg

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