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REVIEW article

Front. Endocrinol., 18 November 2023
Sec. Systems Endocrinology
This article is part of the Research Topic Benefits and Risks of Drug Combination Therapy for Chronic Metabolic Diseases View all 8 articles

Platelet-rich plasma for the treatment of diabetic foot ulcer: a systematic review

Hong OuYangHong OuYang1Yi Tang*&#x;Yi Tang1*†Fan Yang*&#x;Fan Yang1*†Xin RenXin Ren1Jing YangJing Yang1Hongyi CaoHongyi Cao1Yifan YinYifan Yin2
  • 1Geriatric Diseases Institute of Chengdu, Department of Endocrine and Metabolism, Chengdu Fifth People’s Hospital (The Second Clinical Medical College, Affiliated Fifth People’s Hospital of Chengdu University of Traditional Chinese Medicine), Chengdu, China
  • 2Department of Nephrology, Chengdu Third People’s Hospital, Chengdu, China

Background: With the increasing incidence of diabetes, diabetic foot ulcer(DFU) has become one of the most common and serious complications in people with diabetes. DFU is associated with significant morbidity and mortality, and can also result in significant economic, social and public health burdens. Due to peripheral neuropathy, peripheral vascular disease, hyperglycemic environment, inflammatory disorders and other factors, the healing of DFU is impaired or delayed, resulting in the formation of diabetic chronic refractory ulcer. Because of these pathological abnormalities in DFU, it may be difficult to promote wound healing with conventional therapies or antibiotics, whereas platelet-rich plasma(PRP) can promote wound healing by releasing various bioactive molecules stored in platelets, making it more promising than traditional antibiotics. Therefore, the purpose of this systematic review is to summarize and analyze the efficacy of PRP in the treatment of DFU.

Methods: A literature search was undertaken in PubMed, CNKI, EMB-ASE, the Cochrane Library, the WanFang Database and the WeiPu Database by computer. Included controlled studies evaluating the efficacy of PRP in the treatment of diabetic foot ulcers. The data extraction and assessment are on the basis of PRISMA.

Results: Twenty studies were evaluated, and nineteen measures for the evaluation of the efficacy of PRP in DFU treatment were introduced by eliminating relevant duplicate measures. The efficacy measures that were repeated in various studies mainly included the rate of complete ulcer healing, the percentage of ulcer area reduction, the time required for ulcer healing, wound complications (including infection rate, amputation rate, and degree of amputation), the rate of ulcer recurrence, and the cost and duration of hospitalization for DFU, as well as subsequent survival and quality of life scores. One of the most important indicators were healing rate, ulcer area reduction and healing time. The meta-analysis found that PRP was significantly improve the healing rate(OR = 4.37, 95% CI 3.02-6.33, P < 0.001) and shorten the healing time(MD = -3.21, 95% CI -3.83 to -2.59,P < 0.001)of patients with DFU when compared to the conventional treatment, but there was no significant difference in reducing the of ulcer area(MD = 5.67, 95% CI -0.77 to 12.11,P =0.08>0.05 ).

Conclusion: The application of PRP to DFU can improve ulcer healing rate and shorten ulcer healing time, but more clinical data are needed to clarify some efficacy measures. At the same time, a standardized preparation process for PRP is essential.

Introduction

The global incidence of diabetes is increasing rapidly. The International Diabetes Federation(IDF) estimates that the prevalence of diabetes will increase from 10.5%(536.6 million people in the 20-79 age group) in 2021 to 12.2%(783.2 million people in the 20-79 age group) by 2045 (1). It is projected that nearly half of adults (44.7 percent; 239.7 million people in the 20-79 age group) do not know they have diabetes, and people may be more susceptible to microvascular and macrovascular complications in an asymptomatic diabetic state (2).

Diabetic foot ulcer (DFU) is one of the most common and serious complications in patients with diabetes (36) and is characterized by complex management, high morbidity, and high mortality (7). The annual incidence of diabetic foot around the world ranges from 9.1 million to 26.1 million (8, 9), with a global prevalence of about 6.3%, which mostly occurs in patients with type 2 diabetes, the elderly, and people with a longer duration of diabetes (10). In China, the prevalence of DFU is increasing with the increase of the incidence of diabetes year by year. According to statistics, the incidence of DFU in people over 50 years old in China is as high as 8.1% (3, 11). DFU continue to be an important cause of hospitalization in patients with diabetes and form the basis of 40-70% of diabetic non-traumatic lower limb amputations (12, 13).

Relevant reports have also shown that nearly 88% of lower leg amputations are associated with diabetic foot ulcers (14). In addition, the global annual cost of DFU treatment and amputation is approximately US $10.9 billion (15), and the cost of DFU treatment in China will rise from the current US $4.9 billion to US $7.4 billion by 2030 (16). Thus, DFU is associated with significant morbidity and mortality, as well as significant economic, social, and public health burdens.

Therefore, the treatment of DFU has become an urgent problem. Currently, the first-line routine treatment for DFU includes blood glucose control, conventional treatment (infection management, debridement, wound discharge, dressing), and angioplasty for ischemic peripheral artery disease (PAD) (17). However, the current treatment of DFU remains unsatisfactory. It has been reported that the median healing time of DFU without surgery is about 12 weeks (18), and about 20% of patients still have no healing after 1 year, with a recurrence rate of 40% in the same year (3). Therefore, the development of a fast, effective, and economical treatment for DFU is an important issue. In recent years, related studies have found that the use of stem cells or growth factors can form the basis of a new treatment, which can restore the body's normal healing process. Of these, PRP is of great interest because platelets possess a variety of growth factors, which are essential for tissue repair and regeneration, and have antibacterial properties in traumatic injuries (19, 20). PRP is a plasma preparation rich in platelets with a higher concentration than whole blood (21). The concentration of platelets in its plasma is above baseline, ranging from 150×103/dL to 400 x103/dL (22), which is 4-5 times higher than in whole blood (23, 24). The classic method of PRP preparation consists of two steps, the first step will be centrifugation to separate the blood components into three layers: a red blood cell layer, a light-colored coating layer (which contains most platelets and white blood cells) and poor quality platelet plasma, and the second step harvests concentrated platelets in a small volume of plasma, called PRP (25). The role of PRP in wound healing is mainly through the release of various bioactive molecules stored in platelets. In recent years, many studies have conducted relevant analysis on the efficacy of PRP in the treatment of DFU, but they are only limited to a few indicators, and there are still different conclusions, such as: Tasmania et al. concluded that the use of PRP in DFU promoted wound healing, reduced ulcer volume, reduced the time to complete wound healing, and reduced the incidence of adverse events, with no difference in the probability of wound complications (26). This is consistent with previous findings (2731). However, Ajay et al. concluded that PRP had no significant effect on promoting ulcer healing (32). As one of the most important and common complications of diabetic patients, DFU has a profound impact on the prognosis, amputation and even death of patients. As a new method to treat DFU, the efficacy of PRP in DFU is worth further study. Therefore, the main purpose of this review is to review the results of various studies on the efficacy of PRP in the treatment of DFU.

Review method

Search strategy

This review was registered at the International Platform of Registered Systematic Review and Meta-analysis Protocols(INPLASY).The registration number was INPLASY2023110003.A literature search was undertaken in PubMed, CNKI, EMBASE, the Cochrane Library, the WanFang Database and the WeiPu Database by computer. The retrieval time was from the establishment of the database to June 2023, using the combination of subject terms and free words. The search terms included "Diabetes", "Diabetic foot ulcer", "Platelet-rich plasma", "Diabetic complications" and "Efficacy”. The search strategies for each database were presented in Appendix 1.

Inclusion and exclusion criteria

The included studies were clinical trials (including randomized controlled trials、case-controlled trials、prospective observational) and retrospective studies (there were no language or location restrictions).We excluded case reports, letters, reviews. We included studies evaluating the efficacy of PRP in the treatment of DFU. Since the conventional first-line treatment of DFU includes blood glucose control, infection management, debridement, wound undressing, dressing, and vascular surgery for PAD (17), therefore, the relevant efficacy indicators included in our study mainly included wound healing rate, healing time, ulcer area reduction rate, ulcer recurrence rate, amputation rate or follow-up surgical treatment rate, infection rate, adverse event, length of stay, hospitalization cost, etc.

Data extraction and quality evaluation

Two evaluators independently searched the database according to the inclusion and exclusion criteria, searched the full text of the initially included literatures, and extracted the literature data using a unified table, including the author's name, publication year, country, study type, research topic, number of studies, research time, main outcome indicators, and research conclusions. The included studies were evaluated from five aspects: randomization method, baseline comparability, intervention measures, blind method, and result analysis by using the Centre for Evidence-Based Medicine at Oxford University, UK. Evaluators made "yes", "no", "unclear" judgments for each evaluation item. We recorded the scores by using a scoring method ranging from 0 to 5, with 1 point for each project. The total score ≤2 points was considered as low-quality research, and ≥3 points was considered as high quality research.

Statistical analysis

We used the Stata or R software for statistical analysis, using relative hazard (RR) and 95% confidence interval (CI) as the evaluation index of the results, represented by mean difference and 95% CI. First, heterogeneity was assessed using the X2 test (a=0.05) and a quantitative analysis of I2 for heterogeneity (I2 ≥ 50%) conducted. In cases of no heterogeneity between the research results, the meta-analysis was conducted. In cases of statistical heterogeneity between the research results, the source of heterogeneity was further analyzed, and the random heterogeneity model was used after excluding the influence of obvious clinical heterogeneity. Funnel maps created using the Stata software were employed to detect publication bias.

Results

Study selection

According to the pre-designed literature search strategy, a total of 482 articles were retrieved by June 2023, and after removing duplicate studies, we found 243. Then after reviewing the title and abstract, another 96 articles were excluded and 147 articles were reviewed in detail, of which 86 were deemed likely to qualify for this review. Ultimately, we included 20 studies in this review. The remaining 66 studies were excluded due to a lack of data on the efficacy of PRP in DFU in the full text. We adhered to reporting and conduct guidance based on the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) statement (Figure 1).

Figure 1
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Figure 1 PRISMA flow diagram for the literature search and study selection.

Characteristics of studies

We summarized the basic characteristics of the included studies, as shown in Table 1. The included studies were published between 2005 and 2023, with five studies from Egypt (34, 3840, 48), four from China (41, 44, 45, 52), three each from India (32, 37, 50) and Iran (35, 36, 51), two from the United Kingdom (33, 49), and one each from the United States (43), Pakistan (46), and Lithuania (42). The studies included seven different interventions: fat transplantation, fat transplantation +PRP, PRP, conventional therapy (standard care, saline dressing), hyperbaric oxygen therapy, stem cell transplantation, and stem cell transplantation +PRP. Among them, there were 14 studies comparing PRP with conventional treatment, 2 studies comparing fat transplantation, fat transplantation +PRP with conventional treatment, 1 study comparing different types of PRP, 1 study comparing hyperbaric oxygen and stem cell transplantation with PRP and conventional treatment respectively, and 1 study comparing the effect of PRP on diabetic feet with different wound sizes.

Table 1
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Table 1 Characteristics of Included Reports (n=20).

After quality evaluation, 19 studies scored ≥3 points, and only 1 study scored ≤2 points, which was good included in the study quality. The results were shown in Table 2. Many studies failed to score in the category of blinded or not, possibly because the study of DFU in the PRP group was an open-label study, both the patient and the investigator knew the nature of the study and the assignment of the study group, so a blind approach could not be implemented.

Table 2
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Table 2 The quality assessments of studies.

Overview of the efficacy of PRP in the treatment of DFU

A total of 63 measures of efficacy of PRP for diabetic foot were reported (Table 3). By eliminating the duplicate measures reported in the study, we finally introduced 19 measures for the evaluation of the efficacy of PRP in DFU treatment. The efficacy measures that were repeated in various studies mainly included the rate of complete ulcer healing, the percentage of ulcer area reduction, the time required for ulcer healing, wound complications (including infection rate, amputation rate, and degree of amputation), the rate of ulcer recurrence, and the cost and duration of hospitalization for DFU, as well as subsequent survival and quality of life scores. Among these studies, twelve studies reported the complete healing rate of DFU patients after treatment, the results of meta-analysis showed that the use of PRP resulted in significantly higher complete-healed DFU compared to conventional treatment (OR = 4.37, 95% CI 3.02-6.33, P < 0.001) as shown in Figure 2.1. Five studies reported that the healing time of patients with DFU treated using PRP was significantly shorter compared to conventional treatment (MD=-3.21, 95% CI -3.83 to -2.59,P < 0.001)as shown in Figure 2.2. Four studies reported that the ulcer area of patients with DFU treated using PRP was no significantly reduced compared to conventional treatment(MD=5.67, 95% CI -0.77 to 12.11,P =0.08>0.05 )as shown in Figure 2.3. Figure 3 shows the funnel diagram after adjustments for comparison. Most studies on the funnel plot are symmetrically distributed on both sides of the vertical line at X = 0, indicating no significant publication bias.

Table 3
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Table 3 Primary outcome measures of PRP treatment for DFU.

Figure 2
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Figure 2 Forest plot of the effect of PRP compared with conventional treatment of DFU.

Figure 3
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Figure 3 The funnel plot.

Discussion

DFU is one of the most common, serious and costly complications of diabetes and the leading cause of hospitalization for people with diabetes worldwide (53). DFU is also the main cause of lower limb amputation in diabetic patients, which often leads to disability (54, 55), emotional disorders, socio-economic problems, and severely impaired quality of life, and even death in severe cases (56, 57). Studies have found that about 15%-25% of people with diabetes have experienced DFU during their lifetime (3, 5759).

Through meta-analysis, we found that compared with conventional or standard care, the use of PRP in DFU can effectively improve the ulcer healing rate, and shorten the ulcer healing time, which is consistent with the results of previous studies (34, 3740, 43, 46, 48). However, there was no significant difference in reducing the increase of ulcer area, which may be due to the small number of included study data and large heterogeneity.

In addition, a study has found that PRP can still effectively promote the healing of DFU and shorten the healing time after excluding factors such as age, gender, smoking status and blood pressure status of diabetic patients, but had no significant effect on reducing the need for amputation, the level of amputation, or the need for further treatment (such as graft or angioplasty) (35). He et al. divided PRP into autogenous PRP(au-PRP)and allogeneic PRP(al-PRP), and found that PRP in both groups could effectively and safely promote wound healing in DFU compared with conventional dressing treatment, suggesting that al-PRP could be used as a ready solution for DFU when au-PRP was limited (45). The efficacy of PRP is also different among ulcers of different sizes. Babaei et al. 's prospective study grouped diabetic foot wounds according to the size of ulcers and found a significant difference in wound healing time, which was related to the size of ulcers. Patients with the smallest ulceration group (2-5.5cm2) had faster wound healing time than those with the largest ulceration group (8.5-12.5cm2).According to this study, PRP is not recommended for large, non-healing ulcers in DFU, and skin graft must be used as the final method of wound healing (36). In the long-term follow-up of patients, Li et al. found that there was no significant difference in the long-term recurrence rate of ulcers between the PRP group and the control group (44). We collected meta-analyses related to PRP treatment of skin ulcers in the past 5 years and summarized them, as shown in Table 4. The results showed that PRP had a positive effect on promoting ulcer healing in the treatment of chronic skin ulcers, including DFU, venous ulcers of lower extremities and pressure ulcers. In two recent meta-analyses, Gong and Peng et al. found that PRP treatment of DFU increased the possibility of wound healing, reduced the ulcer volume, and reduced the time of complete wound healing (28, 63). This is consistent with the results of our meta-analysis. Secondly, the meta-analysis of Tasmania also showed that in terms of safety, platelet-rich plasma and standard treatment had no difference in the probability of wound complications or recurrence, but overall reduced the incidence of adverse events (26). These results are consistent with the findings of the meta-study by Dai,Qu (2731, 62). Although there is no same conclusion about whether or not DFU treated by PRP has the same effect on patients' later amputation and the degree of amputation, it has been found in related studies that the overall amputation rate of DFU patients in PRP group is lower (62). PRP alone is used to treat DFU, which can effectively increase the healing rate of ulcers and shorten the healing time. In addition, relevant studies have also found that when PRP is combined with other treatment modalities, it can also work to a certain extent. Some studies reported that the addition of PRP to fat grafts resulted in increased angiogenesis in fat grafts and thus improved the viability of fat graft cells (33, 47, 49, 52, 60, 61, 6467). In another study, the addition of PRP to mesenchymal stem cells also observed significant neovascularization and more significant wound reduction (51). Yin et al. found that VSD combined with PRP could also significantly shorten the healing time and improve the healing rate of ulcers (68).

Table 4
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Table 4 Meta-analysis of PRP treatment for chronic wounds.

The activity of PRP is related to many factors in the preparation process, which to some extent affects the efficacy of PRP in the treatment of diabetic foot. We summarized the factors related to PRP preparation in the included studies, as shown in Table 5. We can find that an important factor affecting the preparation of PRP is the centrifuge conditions, such as force and duration, which are significantly different in different studies. Another important factor is the difference in activators, and different activators may affect the release of bioactive molecules and the cleavage of fibrinogen. In addition, we can see that PRP preparation is mostly extracted from patients' peripheral blood, and there are individual differences among different patients, which may also cause different PRP activities prepared under the same preparation conditions.

Table 5
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Table 5 Factors related to PRP preparation in the study.

PRP for diabetic foot can effectively reduce the ulcer area, improve the ulcer healing rate, and to a certain extent reduce the infection rate of the wound and reduce the occurrence of complications. The reason why PRP can play such a curative effect is on the one hand due to the particularity of DFU healing, on the other hand, it depends on the mechanism of PRP. Changes in the micro-environment due to diabetes mellitus (DM) alter normal cell recruitment and activation and lead to impaired or delayed wound healing (6971). In this way, the wound is disconnected from the normal process and does not heal for a long time, resulting in the formation of diabetic chronic refractory ulcers. At present, it is generally believed that peripheral neuropathy and peripheral vascular disease are the two main factors causing foot ulcers in diabetic patients (72). Secondly ,the hyperglycemic environment in diabetics also leads to increased production of advanced glycation end products (AGEs) and continued elevated levels of inflammatory cytokines (i.e., interleukin (IL-1ß) and tumor necrosis factor a (TNF-a), thus impedes the normal wound healing process (73, 74). At the same time, hyperglycemia also leads to an increased risk of infection, and the rapid spread of infection and high microbial burden also adversely affect the wound healing process. In addition, inflammation disorders are also a hallmark of diabetes and underlie many complications of diabetes, including diabetic ulcers (75). Given these pathological abnormalities present in diabetes, it is recommended that specific synthetic growth factors be used topically to manage diabetic foot ulcer wounds. PRP's effect on wound healing is mainly through the release of various bioactive molecules stored in platelets, including PDGF, transforming growth factor β(TGF-β), VEGF, epithelial growth factor (EGF), and adhesion molecules such as fibrin, fibronectin, and hyalenin (76, 77). These factors are known to regulate processes such as cell migration, attachment, proliferation, and differentiation, and to play an important role in wound healing and regeneration by binding to specific cell surface receptors to promote the accumulation of extracellular matrix(ECM) (76, 7880). In addition to growth factors, PRP include many important proteins, such as fibrin, which not only provide scaffolds for tissue regeneration, but also promote wound contraction, blood clotting, and wound closure (81, 82). In addition, activated PRP contains a variety of antibacterial proteins. Previous studies have shown that activated PRP can inhibit staphylococcus aureus, staphylococcus epidermidis, escherichia coli, klebsiella pneumoniae, and methicillin-resistant staphylococcus aureus , without drug resistance, and has synergistic effects with antibacterial agents (8385). The combination of these action characteristics makes PRP more promising than conventional antibiotic prescribing (85).

Limitations

In this study, employed a comprehensive search strategy for key review tasks that contains all of the studies that assessed the efficacy evaluation of PRP for DFU, however, it is possible that some unpublished data were missed. Second, there are too few data on some indicators of the efficacy of PRP in DFU treatment (such as amputation rate, degree of amputation, and need for further treatment (tissue transplantation or angioplasty), so more clinical data are needed for further study.

Conclusion

PRP can release various bioactive molecules and antibacterial proteins, which makes it effective in improving ulcer healing rate and shortening ulcer healing time when used in DFU. In the future, more studies are needed to further explore the efficacy of PRP. Secondly, the efficacy of PRP in the treatment of DFU is largely affected by various factors in the preparation process, so a standardized preparation process is essential.

Author contributions

HO: Investigation, Methodology, Writing – original draft, Writing – review & editing. YT: Writing – review & editing. FY: Writing – review & editing. XR: Data curation, Writing – review & editing. JY: Methodology, Writing – review & editing. HC: Formal Analysis, Writing – review & editing. YY: Validation, Writing – review & editing.

Funding

This project was supported by the Research and Development of intelligent system for sustainable Lifestyle Management of overweight or obese people of Chengdu Science and Technology Department(No. 2022-YF05-01340-SN) ,the Study on the efficacy and safety of different low carbohydrate diet patterns in the remission of Type 2 diabetes Mellitus of Chengdu Health Commission (No. : 2022357).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fendo.2023.1256081/full#supplementary-material

Abbreviations

PRP, platelet-rich plasma; APG, autologous platelet-rich; VLUs:venous leg ulcers; DFU, diabetic foot ulcer; RCT, randomized controlled trial; Al-PRP, allogeneic platelet-rich plasma; Au-PRP, autogenous platelet-rich plasma; VSD, vacuum sealing drainage; ECM, extracellular matrix; IDF, international diabetes federation; DM, diabetes mellitus; VEGF, vascular endothelial growth factor; PDGF, platelet-derived growth factor; AGEs, advanced glycation end products; IL-1ß, interleukin; TNF-a, tumor necrosis factor a; PAD, peripheral artery disease; TGF-β, transforming growth factor β; EGF, epithelial growth factor; PRISMA, the Preferred Reporting Items for Systematic Review and Meta-Analysis.

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Keywords: diabetes, platelet-rich plasma, diabetic foot ulcer, therapeutic index, preparation condition

Citation: OuYang H, Tang Y, Yang F, Ren X, Yang J, Cao H and Yin Y (2023) Platelet-rich plasma for the treatment of diabetic foot ulcer: a systematic review. Front. Endocrinol. 14:1256081. doi: 10.3389/fendo.2023.1256081

Received: 10 July 2023; Accepted: 23 November 2023;
Published: 18 November 2023.

Edited by:

Dan Yan, Capital Medical University, China

Reviewed by:

Rania ElBackly, Alexandria University, Egypt
Ajay Vikram Singh, Federal Institute for Risk Assessment (BfR), Germany

Copyright © 2023 OuYang, Tang, Yang, Ren, Yang, Cao and Yin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yi Tang, paopaotangt@163.com; Fan Yang, yangfan102522@qq.com

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.