
Abstract
Introduction: Osteoarthritis (OA) of the knee is the most common chronic degenerative joint diseases affecting the quality of life of patients. Pain and loss of function are the main clinical features that lead to treatment. For middle-aged and older patients with earlier stages of OA, conservative nonsurgical interventions have been proposed to treat the painful joint. More recently, platelet-rich plasma (PRP), a biological therapy, has become a treatment option to improve the status of the joint for patients with OA. The present study evaluated the clinical outcome of photoactivated platelet–rich plasma (PA-PRP) in patients with chronic knee osteoarthritis.
Methods: A total of 232 patients with knee osteoarthritis, aged between 40-70 years were enrolled and treated in the present study and intervention for twelve months. The patients fulfilled the American College of Rheumatology (ACR) criteria for knee OA. The Western Ontario and McMaster Universities OA index (WOMAC) Questionnaires were used for outcome measurement. Results were evaluated after 12 months of intervention.
Results: Female and male patients were 66.8% and 33.2% respectively. Mean age and SD of the patients were 55.69 (± 9.09) and 56.19 (± 9.09) respectively. The mean (SD) score of pain, stiffness and physical function during the 1st visit before treatment were 6.74 (± 3.00), 2.16 (± 1.85) and 22.30 (± 9.17) and after showed 2.44(± 1.66), 0.60 (± 0.74) and 8.84 (± 4.20) respectively.
The total mean WOMAC scores during the first visit and after treatment were 31.21 (± 12.19) and 11.82 (± 5.65) respectively. The total score of reduction was statistically significant after treatment (p=0.00).
The principal findings of the study were that the mean WOMAC score reduced and there was improved pain, stiffness and functional capacity of patients with knee OA.
Conclusion: In conclusion, treatment with PA-PRP for patients with knee osteoarthritis produced beneficial effects in terms of clinical outcomes. These results suggested that PA-PRP might be a valuable therapeutic agent for knee osteoarthritis in Bangladesh.
Key words
photoactivated; platelet-rich plasma; knee osteoarthritis; WOMAC score; regenerative medicine
Introduction
Osteoarthritis is a major cause of knee disability involving cartilage damage related to an inadequate healing response in the inflammatory milieu. Current non-surgical treatment modalities include physiotherapy, analgesia, non-steroidal anti-inflammatory drugs, and intra-articular injections, such as hyaluronic acid, corticosteroid, or Ozone, with the purpose of reducing symptoms and improving joint function [1].
Osteoarthritis (OA) of the knee is one of the most common chronic degenerative joint diseases affecting the quality of life of patients [2]. Knee OA is a degenerative disease that may develop due to aging, trauma, strain, obesity, joint deformity and congenitally abnormal joints [3]. It is caused by many factors such as a degradation of articular cartilage, injury, joint edge and subchondral bone hyperplasia, and ischemia. Knee OA is characterized joint pain, tenderness, stiffness, joint swelling, restricted movement, quadriceps wasting and joint deformity. Pain and loss of function are the main clinical features that lead to treatment [4,5]. Although knee-replacement surgery provides an effective solution for severe knee OA [6], for patients with earlier stages of OA, for young patients, for those with co-morbidities and age-related anaesthetic risk, for those who fear surgery, and for those without access to surgery for socio-economic reasons, conservative, nonsurgical interventions have been proposed to treat the painful joint [7,8]. Conservative nonsurgical interventions include analgesics, non-steroid and steroidal anti-inflammatory oral medications, and corticosteroid and hyaluronic acid (HA) injections. Although these agents may be beneficial in the short term, there is a lack of evidence that such interventions alter the progression of OA, may worsen long-term outcomes or have side effects. More recently, photoactivated platelet-rich plasma has become a treatment option to improve the status of the joint for patients with OA [9-11].
PRP is an autologous blood product that contains high concentrations of growth factors including vascular endothelial growth factors transforming growth factor-β, epidermal growth factor, fibroblast growth factor, and platelet-derived growth factor. These growth factors serve to promote local angiogenesis, modulate inflammation, inhibit catabolic enzymes and cytokines, recruit local stem cells and fibroblasts to sites of damage or injury and induce healthy nearby cells to manufacture greater numbers of growth factors [12-14]. Thus, the local use of PRP directly at the site of cartilage injury is thought to stimulate a natural healing cascade and accelerate the formulation of cartilage repair tissue [15,16].
We hypothesized that PA-PRP injections would be more efficacious for pain relief and functional improvement in the treatment of patients with knee OA.
•Growth factors help synoviocytes to produce more hyaluronic acid and also increase collagen deposition.
•Growth factors make the matrix more resistance to enzymatic degradation.
Material and Methods
Study design: A prospective follow up study for twelve months.
Objective: The present study evaluated the clinical outcome of photoactivated platelet–rich plasma in patients with chronic knee osteoarthritis.
Ethics statement: Our research was conducted in accordance with the principal of the Declaration of Helsinki. All patients were required to review trail protocols and subsequently provided their informed consent. All the participants who signed the consent form they were included in the study.
Study participants: A total of 232 patients with knee osteoarthritis, aged between 40-70 years were enrolled in the present study.
The patients fulfilled the American College of Rheumatology (ACR) criteria for knee OA. Inclusion criteria were arthralgia over the previous 3 months with radiologic evidence of articular damage (grades 1-4of Kellgren-Lawrence scale) [17]. Exclusion criteria included age over 70 years, history of immunosuppressive and collagen vascular disorders, history or presence of cancer or malignant disorders any infection or active wound of the knee, recent history of severe trauma to the knee, autoimmune and platelet disorders, use of NSAIDs 2 days before injection, history of knee articular injections of corticosteroids during the previous 3 weeks or use of systemic corticosteroids 2 weeks before PA-PRP injections, haemoglobin measures of less than 10g/dl and platelet counts of less than 150,000 per micro litre, history of vasovagal shock, pregnancy or breast feeding.
The study participants attended a screening visit that included history taking, physical examination, laboratory testing, knee radiography, standing anterior-posterior (AP), lateral and skyline views and a survey of medications and supplements.
Outcome measures: The most widely used condition- specific instruments for the assessment of knee OA is the Western Ontario and McMaster Universities OA index (WOMAC) [18-20]. The WOMAC questionnaire is a widely used tool in studies of arthritis. It includes five items for pain, two items for stiffness and 17 items for assessing functional limitation [21]. Each question is scored from 0 to 5 with higher scores implying worse patient status. We used the WOMAC questionnaire in our present study.
Photoactivated plasma rich protein: PA-PRP work as three steps repair, regeneration and restore of the damage cell. A 10-minute exposure of PA-PRP to monochromatic light prior to injection. Photoactivation helps growth factor releasing from platelets, increases pro-inflammatory cytokine receptors, IL1 Ra and IL2 Ra, beta-endorphin photo modulation has significant benefit in the biomechanics of tissue regeneration and healing process. One of the largest clinical concerns for patients about PRP treatment is exacerbation of pain at the injected area post treatment and photo activation of PRP has been postulated to overcome this.
Intervention: For the process of PA-PRP preparation patients were referred to the laboratory. The PA-PRP processing was done using the SureCell Kit. The SureCell class two PRP tube maintains sterility throughout the entire process and uses a single spin system. In order to prepare PA-PRP with concentrations of three times the average normal values, 16-18mL of blood was first collected from the patients’ upper limb cubital vein using a 21 G needle and the SureCell PRP kit contains 9:1 ratio Sodium Citrate Anticoagulant. The blood sample was then centrifuged for 10 minutes at 1000rmp resulting in three layers: the lower layer made up of red blood cells, the intermediate layer is composed of white blood cells, and the upper layer is composed of plasma. The buffy coat layer and the plasma layer were later collected and photo-activated for 10 minutes.
The skin of the injection site was prepped and draped and 7-8ml of PA-PRP was injected under sterile conditions using a 25 G needle through the lateral suprapatellar approach in extended knee position. After 10-15 minutes of rest, patients were asked to actively flex and extend their knees so that the PA- PRP could spread evenly throughout the joint space. Patients received the next injection after 1week, 2weeks and 6weeks from the first injection. Patients were evaluated 12 months after the intervention.
Statistical analysis: Final data before and after the treatment was imported and analyzed by SPSS 21 version. Continuous variables were reported as the mean with a 95% confidence interval (CI) and P < 0.005 was considered to indicate a statistically significant difference. For comparing variables with normal distribution, paired t-test was used. Qualitative variables were expressed with frequency and percent. The differences between before and after treatment were presented in a Box and Whisker diagram where “X” and “Horizontal line” in the box indicate the “mean” and “median” of the total score respectively.
A total 232 knee osteoarthritis patients were treated by PRP where 66.8% (155) were female and 33.2% (77) were male. In the initial visit before and after PRP treatment the mean age and SD of the respondent was 55.69 (± 9.09) and 56.19 (± 9.09) respectively. Body mass index before and after were 30.02 (± 3.09) and 29.21 (± 3.33) respectively and statically significant (p=0.00) (Table. 1).
Table 1: Baseline characteristics of the study subjects (N = 232).
Variable |
Study group |
P-value |
|
1st visit |
12-month follow up |
||
Sex |
232 |
232 |
– |
Female (%) |
155 (66.8) |
155 (66.8) |
– |
Male (%) |
77 (33.2) |
77 (33.2) |
– |
Age, mean ± SD |
55.69 ± 9.09 |
56.19 ± 9.09 |
– |
BMI, mean ± SD |
30.02 ± 3.90 |
29.21 ± 3.33 |
0.00 |
The initial assessment was done by WOMAC scoring methods. Scoring was done under pain, stiffness and physical function domains. The higher score indicates the more disability. The total score was calculated by the sum of pain, stiffness and physical function. The highest total score was 96 according to the WOMAC scale. The mean (SD) score of pain, stiffness and physical function during the 1st visit before treatment were 6.74 (± 3.00), 2.16 (± 1.85) and 22.30 (± 9.17) respectively. After 12 months treatment of PA-PRP treatment, the score was calculated again and showed 2.44 (± 1.66), 0.60 (± 0.74) and 8.84 (± 4.20) in terms of pain, stiffness and physical function respectively (Table. 2).
Table 2. Comparison between before and after the study subject.
Variable |
Study group |
P-value |
|
1st visit |
12-month follow up |
||
WOMAC, mean, SD | |||
Pain |
6.74 ± 3.00 |
2.44 ± 1.66 |
0.00 |
Stiffness |
2.16 ± 1.85 |
0.60 ± 0.74 |
0.00 |
Physical Function |
22.30 ± 9.17 |
8.84 ± 4.20 |
0.00 |
Total |
31.21 ± 12.19 |
11.82 ± 5.65 |
0.00 |
The total WOMAC scores during the initial visit and after treatment were 31.21 (± 12.19) and 11.82 (± 5.65) respectively. Total score reduced significantly after treatment with PRP (p=0.00) (Figure. 1).
Figure 1: Box and whisker plot of total before and after score (total mean)
The total WOMAC score in the different age and gender groups is reduced significantly after PA-PRP treatment of the respondents. In the different age categories, the mean difference showed reduction of 20.85, 17.92, 16.89 and 16.49 respectively and statistically significance of (p=0.00) (Table. 3).
Table 3: Difference of total score in respect to age and sex.
Variables |
Number |
1st visit |
12-month Follow-up |
Mean difference |
p-value |
||
Age (years) |
Mean |
SD |
Mean |
SD |
|||
up to 40 |
14 |
29.64 |
13.64 |
8.79 |
6.42 |
20.85 |
– |
41 to 50 |
51 |
30.39 |
11.74 |
12.47 |
6.38 |
17.92 |
0.00 |
51 to 60 |
95 |
31.15 |
12.57 |
14.26 |
5.26 |
16.89 |
– |
61 to 70 |
72 |
32.17 |
11.89 |
15.68 |
5.27 |
16.49 |
– |
Discussion
A total of 232 patients with knee osteoarthritis aged 40-70years were enrolled for PA-PRP intervention. It was a prospective follow up study for twelve months. The mean age and SD of the respondents for the first visit and after twelve months of PA-PRP treatment were 55.69 (± 9.09) and 56.19 (± 9.09) respectively. Female and male were 66.8% (155) and 33.2% (77) respectively. Body mass index before and after were 30.02 (± 3.09) and 29.21 (± 3.33) respectively and statically significant (p=0.00). The total WOMAC score during the initial visit and after treatment were 31.21 (± 12.19) and 11.82 (± 5.65) respectively. Total score reduced significantly after treatment with PA-PRP (p=0.00). In the different age categories, the mean reductions in score were 20.85, 17.92, 16.89 and 16.49 respectively and were statistically significant (p=0.00).
Currently WHO estimated that 10% of men and 18% of women have a painful OA worldwide, and 18 million people of Bangladesh suffering osteoarthritis problem. Our result showed female were suffered more OA of knee than male.
The principal findings of the study show that at twelve months post injection the WOMAC score reduced associated with improved pain, stiffness and functional capacity of patients with knee OA. Our results were similar to the study of Wang- Saegusa et al. [22] and Seyed Ahmad Raeissadat et al. [21].
The present author Seyed Ahmad Raeissadat et al. [21] had previously studied the clinical application of PRP and observed efficacy without adverse events. It was a prospective study published in 2013 on 60 patients treated with two injections of PRP (1 every 4 weeks). Patients underwent clinical evaluation at the beginning and at 6 months follow up. The clinical outcomes revealed a statistically relevant improvement in all the variables of WOMAC and SF-36. In our study we did not work with SF-36,
The systemic review included 14 RCTs and assessed the temporal effect of PRP on knee pain and physical function in the treatment of knee OA compared with other intra-articular injections, including saline, HA, Ozone, and corticosteroid. Data synthesis consistently showed intra-articular PRP injections significantly reduced knee pain, improved physical function and total WOMAC scores compared with control [1]. These reviews showed similar result and reduces WOMAC scores.
PA-PRP is a prominent biomedical blood product that produces efficient outcomes for the treatment of patients with knee osteoarthritis and cartilage disorders [23]. As PA-PRP has been approved as an agent for knee osteoarthritis therapy, it is important for clinicians to understand the clinical indications and outcomes in order to maximize the therapeutic benefits of PA-PRP. The present study revealed that repeated administration of PA-PRP relieved the clinical symptoms of knee osteoarthritis. A previous report indicated that inflammatory cytokines from a complex regulatory signal network in osteonecrosis are mediated by intracellular kinase signalling pathways to regulate recruitment, stimulation and activation of autoimmune cells [24]. Although the causes of knee osteoarthritis are not fully understood, laboratory and clinical evidence have suggested that inflammatory cytokines may contribute to its pathogenesis. Theoretically blocking inflammatory factor pathways may interrupt the inflammatory process and limit joint damage.
Furthermore, the stimulatory effects of PA-PRP treatment have been demonstrated to promote proliferation and chondrogenic differentiation, which may produce beneficial molecules for the maintenance of auricular cartilage [25]. The results of the present study suggest that PA-PRP treatment has a major role to play in the management of OA of the knee in Bangladesh.
Study Limitation
The limitations of our study were the lack of a control group and the relatively small sample size. The best PA-PRP concentration, long-term effects, the number of injections and the interval between treatments and the cost effectiveness of PA-PRP are the issues that necessitate more studies in comparison to control groups and other current treatments. In addition, performing objective studies such as MRI and pathologic assessments would be useful in evaluation the mechanism of action of PA-PRP in patients with OA.
Conclusion
The principal findings of the study show that at twelve months post injection WOMAC scores reduced with improved pain, stiffness and functional capacity of patients with knee OA.
According to the study result and considering side effects of analgesic and anti-inflammatory medications, PA-PRP injection can be considered a safe and useful therapeutic option in selected patients with mild-to-moderate degrees OA.
In conclusion, treatment with PA-PRP for patients with knee osteoarthritis produced beneficial effects in alleviating joint inflammation, cartilage destruction, bone damage and repairing joint tissue. These results suggested that PA-PRP may be a valuable therapeutic option for knee osteoarthritis.