Nooh Mohammad H, Alshehri Mohammed S, Alzahrani Ziyad S, Alsolami Hatem M, Almutairi Amal O, AlOtaibi Abdulaziz S, Aljohani Abdulaziz N
Medicine, King Saud Bin Abdulaziz University for Health Sciences, Jeddah, SAU.
Medical Research, King Abdullah International Medical Research Center, Jeddah, SAU.
Cureus. 2023 Jun 30;15(6):e41240. doi: 10.7759/cureus.41240. eCollection 2023 Jun.
Osteoarthritis is a chronic degenerative joint disease that affects weight-bearing joints. Low molecular weight fraction of 5% (LMWF-5A) human serum albumin is an intra-articular injection that emerged for the treatment of knee osteoarthritis. The aim of this review is to assess the efficacy and safety of LMWF-5A versus placebo through a systematic review and meta-analysis. The Cochrane Central Register of Controlled Trials (CENTRAL), Medical Literature Analysis and Retrieval System Online (MEDLINE), EBSCO, and ClinicalTrials.gov registry databases were utilized to search for studies. Only randomized controlled trials (RCTs) that evaluated the efficacy of LMWF-5A versus placebo were included. Efficacy endpoints were represented by Western Ontario and McMaster Universities Arthritis Index (WOMAC) A and C scores for pain and function, respectively. Serious adverse events (SAEs), non-serious adverse events (NSAEs), and mortality rates were used to evaluate the safety of the drug. The revised Cochrane risk of bias tool was used for the risk of bias assessment. Seven RCTs (n=2939) that met the inclusion criteria were included. The meta-analysis did not find significant improvement in pain (WOMAC A) (standardized mean difference (SMD)= -0.01, 95% confidence interval (CI) -0.10 - 0.09, P=0.87, I²=30%). Additionally, no significant change in function was noted (WOMAC C) (SMD=0.01, 95% CI -0.08 - 0.10, P=0.87, I²=22%). The pooled analysis did not find a significant difference between LMWF-5A and placebo regarding the incidence of joint swelling (P=0.84), joint stiffness (P=0.53), arthralgia (P=0.53), extremity pain (P=0.45), NSAEs (P=0.21), SAEs (P=0.92), or mortality (P=1.00). However, the subgroup analysis showed a significant reduction of 42% in NSAEs upon administration of 10 mL of LMWF-5A (risk ratio (RR)=0.58, 95% CI 0.35-0.97, P=0.04). In summary, our meta-analysis did not find significant differences between LMWF-5A and placebo regarding the incidence of NSAEs, SAEs, or mortality. On the other hand, LMWF-5A did not demonstrate superiority over saline in terms of efficacy. Therefore, it is not an effective drug for managing knee osteoarthritis.
骨关节炎是一种影响负重关节的慢性退行性关节疾病。5%低分子量组分(LMWF - 5A)人血清白蛋白是一种用于治疗膝关节骨关节炎的关节内注射剂。本综述的目的是通过系统评价和荟萃分析评估LMWF - 5A与安慰剂相比的疗效和安全性。利用Cochrane对照试验中央注册库(CENTRAL)、医学文献分析与联机检索系统(MEDLINE)、EBSCO和ClinicalTrials.gov注册数据库检索研究。仅纳入评估LMWF - 5A与安慰剂疗效的随机对照试验(RCT)。疗效终点分别由西安大略和麦克马斯特大学骨关节炎指数(WOMAC)A和C评分表示疼痛和功能。严重不良事件(SAE)、非严重不良事件(NSAE)和死亡率用于评估药物安全性。采用修订的Cochrane偏倚风险工具进行偏倚风险评估。纳入了7项符合纳入标准的RCT(n = 2939)。荟萃分析未发现疼痛(WOMAC A)有显著改善(标准化均数差(SMD)= -0.01,95%置信区间(CI)-0.10 - 0.09,P = 0.87,I² = 30%)。此外,功能方面未发现显著变化(WOMAC C)(SMD = 0.01,95% CI -0.08 - 0.10,P = 0.87,I² = 22%)。汇总分析未发现LMWF - 5A与安慰剂在关节肿胀发生率(P = 0.84)、关节僵硬(P = 0.53)、关节痛(P = 0.53)、肢体疼痛(P = 0.45)、NSAE(P = 0.21)、SAE(P = 0.92)或死亡率(P = 1.00)方面存在显著差异。然而,亚组分析显示,给予10 mL LMWF - 5A后NSAE显著降低42%(风险比(RR)= 0.58,95% CI 0.35 - 0.97,P = 0.04)。总之,我们的荟萃分析未发现LMWF - 5A与安慰剂在NSAE、SAE或死亡率发生率方面存在显著差异。另一方面,LMWF - 5A在疗效方面未显示出优于生理盐水。因此,它不是治疗膝关节骨关节炎的有效药物。