Background
Knee osteoarthritis (KOA) is a common knee degenerative disease characterized by cartilage degeneration, cartilage exfoliation, and subchondral bone hyperplasia, leading to knee pain, joint instability and functional limitations [
1]. KOA severely affects patients’ quality of life and is a major public health issue [
2]. An epidemiological survey published in Proceedings of the National Academy of Sciences (PNAS) showed that the incidence of KOA in the U.S. population has doubled since the mid-twentieth century [
3]. KOA has become a high-incidence human disease and has caused a great negative impact on people’s lives and work.
The Osteoarthritis Society International (OARSI) recommends conservative treatment rather than surgery as the first-line management solution for KOA, which emphasizes the importance of conservative treatment in the treatment of KOA [
4]. The American College of Rheumatology (ACR) has proposed a classification in which conservative treatment includes drug treatment and non-drug treatment [
5]. Non-drug treatment includes general exercise and muscle exercise, but non-drug methods often depend heavily on patient compliance and are difficult to control [
5]. The main drug therapies include analgesics, non-steroidal anti-inflammatory drugs and corticosteroid injections [
6]. Although the above drug therapies are effective to a certain degree, there are also major side effects [
6,
7]. In recent years, there have been an increasing number of studies on the application of intra-articular injection of platelet-rich plasma (PRP) or hyaluronic acid (HA) in the treatment of KOA. Many systematic reviews suggest that intra-articular injection of PRP, compared to HA, can alleviate pain symptoms and improve knee function in patients with KOA [
6,
8,
9]. However, a double-blind randomized controlled trial with a 5-year follow-up showed that the combination of HA and PRP improved pain and function in patients with a history of chronic symptomatic knee degenerative changes and osteoarthritis [
10]. An RCT showed that PRP is an effective treatment for mild to moderate KOA and that the combined use of HA and PRP is better than the use of HA (1 year) and PRP (3 months) alone [
11]. The RCT also revealed that PRP does not provide better overall clinical improvement than HA in terms of symptom-function improvement at different follow-up points or in terms of duration of effect [
10]. In recent years, an increasing number of studies have focused on the rationality of PRP combined with HA for KOA, and their mechanisms have been discussed in depth. Experimental studies comparing the migration capabilities of tendon cells and synovial fibroblasts in pure PRP solution and PRP plus HA solution have shown that mixing PRP with HA can significantly improve cell mobility [
12]. Marmotti found that the addition of HA to PRP can effectively promote the proliferation of chondrocytes and improve the ability of cartilage repair [
13]. Studies have shown that the combination of PRP and HA may benefit from its different biological mechanisms and facilitate the activity of signal molecules such as inflammatory molecules, catabolic enzymes, cytokines and growth factors, thereby playing a positive role in the treatment of KOA [
11,
14]
.
In recent years, clinical workers have begun treating KOA with intra-articular injections of HA combined with PRP to take advantage of their synergistic therapeutic effects. The purpose of this study was to explore the efficacy and safety of intra-articular injection of PRP combined with HA compared with PRP or HA alone, providing an evidence-based strategy for the treatment of KOA.
Methods
This meta-analysis was performed strictly in accordance with the relevant requirements of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement.
Inclusion and exclusion criteria
Inclusion criteria. (1) Type of study: Published randomized controlled trial (RCT) or cohort study. (2) Research subjects: Individuals with a clear diagnosis of KOA, regardless of age, gender or nationality. (3) Intervention: Administration of intra-articular injection of PRP combined with Ha to the test group and intra-articular injection of PRP or HA to the control group. Two- or three-arm studies were eligible. (4) At least one of the following outcome indicators: Western Ontario and McMaster Universities Arthritis Index (WOMAC), Lequesne Index, visual analogue scale (VAS), and adverse events (AEs). (5) No application of language exclusions.
Exclusion criteria. (1) Reviews, meeting abstracts, case reports. (2) Subjects with both KOA and hip osteoarthritis. (3) Studies in which the intervention did not include intra-articular injection of PRP combined with HA. (4) Duplicate publications or studies with similar data. (5) Incomplete, unclear, or obviously erroneous data that could not be resolved by contacting the authors.
Literature retrieval strategy
The PubMed, Cochrane Library, EMBASE and China National Knowledge Infrastructure (CNKI) databases were searched, and RCTs and cohort studies that met the inclusion criteria were included. The retrieval period was from the establishment of each database to December 2019. Two researchers also performed cross-referencing to reduce retrieval errors. The search terms included “platelet-rich plasma”, “PRP”, “hyaluronic acid”, “HA”, “knee osteoarthritis” and “KOA”. See Supplement 1 for the database retrieval strategies.
Literature screening and data extraction
Two orthopaedic surgeons conducted the literature retrieval; the preliminary and secondary screenings of the literature were performed strictly in accordance with the pre-established inclusion and exclusion criteria. The two researchers extracted the data independently, and a third researcher compared their outputs. In the event of an error or difference, the third researcher and corresponding author assisted in the judgement.
The main data extracted in this study included first author, publication year, sample size, intervention measures, ethical approval, gender, age, BMI, follow-up periods, radiographic classification, relevant items for literature quality evaluation and relevant outcome indicators of clinical efficacy and safety.
Risk of bias assessment of the included studies
Regarding RCTs, the Cochrane risk of bias tool was used for quality evaluation [
15]. The tool includes evaluation in seven areas: random sequence generation, allocation blinding, blinding of participants, blinding of outcome measures, incomplete outcome data, selective reporting, and other biases. The risk of bias in each area was judged to be low, high or unclear [
16]. For cohort studies, the Newcastle-Ottawa Scale (NOS) was used for quality assessment. This scale includes three aspects: (1) selection of study groups; (2) ascertainment of exposure and outcome; and (3) group comparability. Studies with scores greater than or equal to 7 were considered to have a low risk of bias, scores of 4 to 6 indicated a moderate risk of bias, and scores less than 4 indicated a high risk of bias.
Statistical analysis
The relative risk (RR) was used to evaluate the effects of binary variables, the standardized mean difference (SMD) was used to evaluate the effects of continuous variables, and 95% confidence intervals (CIs) of the RR and SMD were calculated. Review Manager 5.3.5 software (Cochrane Collaboration, Oxford, UK) was used to calculate the efficacy and safety indicators and their 95% CIs. In addition, for homogeneous data sets, P > 0.1 and I2 < 50% were used as the test standards. When the above two statistical conditions were met, a fixed-effects model was used for the meta-analysis because the pooled effect sizes were relatively homogenous. If one of the above standards did not conform, the homogeneity of the pooled effect size was not ideal, and a random-effects model was applied.
To quantitatively assess whether there are publication biases in different outcome indicators, this study used Stata 14.0 (STATA Corporation, Lakeway, Texas, USA) software to perform Egger’s and Begg’s linear regression tests on the outcome indicators included in the combined analysis of three or more studies.
Discussion
KOA is a disease that can cause lower extremity disability, reduce the quality of life of patients, and seriously affect the physical and mental health of middle-aged and elderly people [
24]. With the ageing of the population, KOA will gradually become a common and frequently occurring disease, which is a major challenge that health systems in various countries need to meet [
25]. The pathogenesis of KOA is still unclear, and there is still no continuous and effective conservative treatment [
10]. For patients with KOA who are successfully treated with conservative treatment, surgical treatment is mostly used. However, surgical treatment is mostly used for patients with severe KOA [
26]. In addition, although PRP combined with HA for KOA may be complicated and even more expensive, perhaps compared with the cost and risk of surgery, PRP combined with HA may be a better choice. However, a cost-effectiveness study of PRP combined with HA for KOA and PRP or HA alone is still lacking and needs further research. Moreover, surgical treatment has a long recovery period, unavoidable risks of surgery and complications [
27]. Therefore, it is of great significance to study new treatments for KOA. In recent years, intra-articular injection of PRP or HA for the treatment of KOA has attracted strong interest from many clinicians, and in-depth research has been conducted [
28,
29].
PRP is extracted by centrifugation from autologous blood, and the platelet concentration can be increased nearly 10-fold, which contains approximately 1500 proteins that can release macrophages and growth factors after activation, which is beneficial not only for removing necrotic tissue and reducing the inflammatory response but also for articular cartilage repair and regeneration [
30‐
32]. HA is a high molecular weight polysaccharide that is an important part of synovial fluid and articular cartilage. Injecting HA into the knee joint cavity can physically lubricate the articular surface, reduce wear, and biologically nourish articular cartilage and promote the synthesis of endogenous HA, thereby delaying further joint disease [
33‐
35]. A large number of RCTs and systematic reviews of the intra-articular injection of PRP or HA for KOA have been published [
8,
36‐
38], and most studies have concluded that intra-articular injection of PRP, compared with HA, can relieve knee pain and improve the function of patients with KOA. Moreover, research has shown that the combined application of PRP and HA can repair the degeneration of cartilage and delay the progression of KOA [
11,
14,
39]. This synergistic effect mainly changes the role of inflammatory cytokines in the process of chondrocyte degeneration through specific mediators (CD44, TGF-βRII), thereby promoting cartilage regeneration and inhibiting the inflammatory response [
40].
In this study, a meta-analysis showed that there was no significant difference between PRP combined with HA and PRP alone for KOA at 1 month or 3 months after treatment. This outcome shows that the effects of the two intervention methods in relieving knee pain are similar at 1 month and 3 months after treatment. However, the VAS score at 6 months after treatment showed that intra-articular injection of PRP combined with HA, compared with PRP alone, could relieve pain in patients with KOA. Intra-articular injection of PRP combined with HA has a unique advantage in the long-term relief of pain in patients with KOA, but the results from longer follow-up periods are still needed for comparison. This meta-analysis found that PRP combined with HA at 6 months after treatment was superior to PRP alone, which may suggest that PRP combined with HA may be a better treatment for patients with long-term knee pain in the future. Previous studies have shown that PRP combined with HA for KOA can reduce WOMAC pain scores more than PRP alone can, which is consistent with the present findings [
18]. In terms of the improved WOMAC Function Score and WOMAC Total Score, intra-articular injection of PRP combined with HA, compared with PRP alone, can improve patients’ knee joint function scores and overall WOMAC scores. Studies have reported that compared with PRP alone, HA combined with PRP in KOA treatment significantly improves physical function at 1 and 3 months after treatment [
11]. From the analysis of Lequesne Index scores, it was found that PRP combined with HA reduced the Lequesne Index scores more than PRP alone did, which showed that PRP was more effective in relieving knee pain. This systematic review compared and analysed the adverse reactions of PRP combined with HA compared with PRP and HA alone for KOA. The results showed that no significant difference was found in the incidence of adverse reactions, whether PRP, HA, or both were applied, indicating that the safety of the three treatments was not different. The meta-analysis conducted Begg’s and Egger’s tests on VAS after 1 month and 6 months of treatment and AEs. The results suggest that there was no publication bias, indicating that the above results are reliable.
This study is the first systematic evaluation of the efficacy and safety of PRP combined with HA compared with that of PRP or HA alone for KOA. Additionally, this meta-analysis systematically summarizes the preparation process of the combined application of PRP and HA. Studies have shown that HA is not effective for patients with severe KOA disease, and the effect of HA decreases with time, especially in elderly patients [
41,
42]. HA mainly provides nutrition and protection to joints and cannot regenerate damaged cartilage, while PRP contains a large number of growth factors that can promote chondrocyte proliferation and cartilage matrix synthesis [
40]. Therefore, the combination of PRP and HA may have a better effect in patients who are elderly, have severe KOA, or exhibit a poor response to treatment with HA or PRP alone.
Nevertheless, several limitations were unavoidable. First, 2 articles were non-RCTs, which may have led to heterogeneity of the combined indicators. Second, the follow-up time was short, with the longest follow-up period being 1 year, and the long-term efficacy and safety of PRP combined with HA could not be evaluated. Third, from the indicators related to WOMAC, it was found that due to the inconsistent indicators reported in the literature, the combined results of the indicators related to WOMAC Pain Score and WOMAC Stiffness Score are lacking. In later clinical studies, attention should be paid to the comprehensiveness and consistency of the outcome indicators. Fourth, there are few studies that directly compare the efficacy and safety of the intra-articular injection of PRP combined with HA with those of the intra-articular injection of HA alone. Therefore, this meta-analysis failed to fully compare the efficacy of PRP combined with HA to that of HA alone. Fifth, the inclusion criteria and exclusion criteria of the included literature did not mention information about knee joint conditions, such as ligament instability, meniscus lesions, and alignment of the limb, which may affect the comparability of related data. Sixth, in terms of the KL Score evaluation, due to the limitation of the data included in the literature, the KL classification included grades I to IV, which may affect the credibility of the Lequesne Index evaluation.
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