Melasma is a chronic and recurrent skin problem for which an effective therapy is currently lacking. Platelet-rich plasma (PRP) has recently emerged as a novel treatment for melasma, but to date there has been no systematic evaluation of its efficacy and safety.
Methods
The Web of Science, PubMed, EMBASE, China National Knowledge Infrastructure (CNKI) and the Cochrane Library databases were searched for relevant articles using the search items “melasma,” “chloasma” and “platelet‐rich plasma.” STATA version 15.1 software was used to analyze data. Study outcomes were calculated using standardized mean differences with 95% confidence intervals (CIs).
Results
The database search identified ten studies involving 395 adult patients that met the inclusion criteria and were included in the meta-analysis. Analysis of pre- and post-treatment data from these studies revealed that the post-treatment modified Melasma Area and Severity Index (mMASI) score decreased by 1.18 (95% CI 0.89–1.47; p = 0.02). Subjective satisfaction evaluation of PRP treatment showed that melasma treated with the combination therapy of PRP + microneedling may have been the most efficacious treatment compared to PRP alone or in combination with intradermal injection. Adverse reactions were minor, with only a few patients reporting local congestion, temporary erythema, hyperpigmentation and discoloration.
Conclusion
These results support the efficacy and safety of PRP used in combination or alone as treatment for melasma.
Lingyun Zhao, Meng Hu and Qing Xiao contributed equally to this work.
Key Summary Points
Why carry out this study?
Platelet-rich plasma (PRP) has recently emerged as a novel treatment for melasma.
To date, there has been no systematic evaluation of the efficacy and safety of PRP as a treatment for melasma.
What was learned from the study?
This study showed PRP is a safe and efficient treatment for melasma.
The combination of PRP and microneedle showed the more promising results for melasma treatment.
Introduction
Melasma, also known as “chloasma” or “swarthy spots”, is a common pigmentation disease, mostly presenting as yellowish-brown patches on the face. It commonly occurs in middle-aged women. The etiology of melasma is complex, and related studies have shown that ultraviolet radiation, estrogen level, vascular hyperplasia and skin inflammation are inducing factors [1‐3].
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As melasma is stubborn and prone to relapse, a variety of treatments have been tried, but often with inconsistent results [4, 5]. Topical bleaching is a common treatment, but is often insufficient. Treatment with intense pulsed light or laser has shown conflicting results and certain side effects, such as hyperpigmentation, skin redness and scarring [6]. Previous studies have revealed that melasma is a disease that not only encompasses melanocytes, but also involves derma factors of photoaging [7, 8]. As a result, conventional therapies which focus only on melanosomes or melanocytes may not be sufficient in removing the disease.
Platelet‐rich plasma (PRP) is defined as a small volume of autologous plasma that contains a high concentration of platelets, i.e. well above normal levels, obtained by centrifugation of autologous blood and subsequent suspension of platelets [9]. PRP has been used in the treatment of alopecia, hyperpigmentation, acne and other skin diseases [10]. It is well known that the platelet alpha granules in PRP are rich in growth factors, such as platelet-derived growth factor (PDGF) and transforming growth factor (TGF)-β1 and TGF-β2 [11], which are associated with collagen production, wound healing and homeostasis control.
Recent studies have reported promising results of PRP in the treatment of hyperpigmentation [12‐15]. However, to date there has not been a comprehensive and systematic evaluation of the therapeutic effect of PRP on melasma. We have conducted a systematic review of the literature, with the aim to study the efficacy and safety of PRP in the treatment of patients with melasma when used alone or as an adjuvant therapy and hopefully provide new clinical evidence for the treatment of melasma.
Methods
The procedure used to conduct this systematic review and meta-analysis conforms to the PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) statement [16]. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.
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Database and Search Strategy
Two investigators independently searched the Web of Science, PubMed, EMBASE, China National Knowledge Infrastructure (CNKI) and Cochrane Library databases for original studies that had been published up to and including 23 June 2021, with no language limitation, using the main search terms of “melasma,” “chloasma” and “platelet‐rich plasma.” The search strategy is described in detail in Electronic Supplementary Material (ESM) Table S1.
Inclusion and Exclusion Criteria
Inclusion and exclusion criteria were established by two of the authors (LZ and MH) who assessed each article independently. The inclusion and exclusion criteria are described in detail in ESM Table S2.
Data Extraction
All relevant data in the included studies were independently extracted by two authors (LZ and MH). Detailed information extracted from these studies are presented in Table 1, including the first author’s name, publication year, countries/regions, sample size, mean age of the subjects, the treatment type and follow-up period, primary outcomes and adverse reaction(s). All disputes over data were resolved through discussion.
Table 1
Characteristics of studies included in the meta-analysis
MASI Melasma Area and Severity Index, mMASI modified Melasma Area and Severity Index, PRP platelet-rich plasma
aDosing/treatment schedule is presented in parentheses:Qw once a week, Q2w once every 2 weeks, Q3w once every 3 weeks, Q4w once every 4 weeks, Q8w once every 8 weeks, Q12w once every12 weeks, Q10d once in 10 days
bSubjective evaluation: this includes the doctor's evaluation of the treatment efficacy and the patient's own satisfaction
Quality Assessment
The quality of the eight studies included in the meta-analysis was assessed using the Cochrane risk-of-bias tool (see ESM Fig. S1) in Review Manager (RevMan) Version 5.2. Most studies used controlled experimental designs, but many did not implement strict blind methods or allocation concealment. The outcome data of each study were relatively complete. In summary, the overall quality of the included studies was moderate.
Statistical Analysis
STATA version 15.1 software (StataCorp, College Station, TX, USA) was used in the data analysis. Our main outcome indicator of the efficacy of PRP for the treatment of melasma was the difference in the modified Melasma Area and Severity Index (mMASI) score before and after treatment and subjective assessment of this efficacy. We used a random-effect model to analyze the data, and heterogeneity in pooled studies was tested using the χ2 and I2 tests [17, 18] and categorized into three levels based on the results (low heterogeneity: I2 < 25%, moderate heterogeneity: I2 = 25–75%, high heterogeneity: I2 > 75%). Subgroup analysis and meta-regression including six potential factors (sex, location, treatment type, publication year, age and length of follow-up) were performed to assess the presence of heterogeneity in the included studies. A sensitivity analysis was conducted to reflect the impact of individual studies on the overall results. Potential publication bias of included studies was assessed using Begg’s and Egger’s tests. p values < 0.05 were considered to indicate statistical significance for all analyses.
Results
Search Results
A comprehensive and detailed search of the Web of Science, PubMed, CNKI, EMBASE and Cochrane Library databases identified 31 studies; this number was reduced to 16 articles after duplicate articles were removed. Following a detailed study on all the titles and abstracts of these 16 articles, we eliminated two clinical trials that had not yet completed reporting results. The remaining 14 full-text studies were evaluated for whether they met the inclusion criteria. A further four articles were excluded for the lack of essential information. Ultimately, ten studies were included in the data integration for MASI scores and subjective evaluation [19‐28]. The inclusion and exclusion process of the studies is shown in Fig. 1.
Fig. 1
PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) flowchart of the selection of articles on platelet-rich plasma in the treatment of melasma
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Study Characteristics
The main characteristics of the included studies are presented in Table 1. The year of publication ranged from 2018 to 2021. In terms of study design, there were four RCTs [19‐22], three split‐face trials [23, 24, 27] and three self-controlled trials [25, 26, 28]. Thelocations of these trials were China (3 trials), India (2 trials), Egypt (3 trials), Thailand (1 trial) and Pakistan (1 trial). The studies taken together included a total of 395 patients with melasma. All of the included cases/patients were adults, 90% of whom are women. Melasma severity was assessed by the MASI and subjective evaluation (2 studies with the mean MASI score, 7 studies with the mMASI score, 8 studies with the subjective evaluation). Three therapeutic regimens were used for PRP treatment: microinjection (1 study), microneedling (2 studies), intradermal injection (8 studies). The treatment time ranged from approximately 4 to 12 weeks.
Effects of Interventions
Analysis of Change in MASI Score
Nine studies reported a reduction in MASI score, defined as the difference in MASI score pre- and post-treatment. For studies with combination therapy, we approximately evaluated the efficacy of PRP treatment alone by subtracting the efficacy of the control group. Regarding PRP treatment for melasma, the standardized mean reduction in mMASI score was 1.18 (95% confidence interval 0.89–1.47; p = 0.02; I2 = 54.8%), as shown in Fig. 2. To assess a potential explanation for the moderate heterogeneity (p = 0.02; I2 = 54.8%), we conducted a sensitivity analysis, a subgroup analysis and meta-regression analysis. The sensitivity analysis showed that the analysis was stable except for one study [25]; the heterogeneity test results after removing this study were I2 = 0%, p = 0.492. After removing this study from the analysis, we found no significant differences between the subgroups as well as the smallest p value (0.4; p > 0.05 (ESM Table S3). The meta-regression analysis also suggested no differences in publication year, age and time of treatment (publication year: p = 0.778; age: p = 0.419; duration of treatment: p = 0.421). Finally, Begg’s (p = 0.92) and Egger’s (p = 0.95) tests indicated that publication bias cannot be considered.
Fig. 2
Forest plot showing the comparisons of the change in Melasma Area and Severity Index (MASI) score post- and pre-treatment in nine studies on treatment with platelet-rich plasma (PRP) alone. CI Confidence interval, SMD standardized mean difference
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Analysis of Subjective Evaluation
As mentioned earlier in this article, the subjective evaluation includes the doctor's evaluation of the treatment efficacy and the patient's own satisfaction with the treatment. We calculated the average value of the subjective evaluation data included in each group and plotted it in Fig. 3. Overall evaluation of the efficacy of PRP revealed that nearly one third of the participants had an excellent response and two thirds reported a high satisfaction level (including “excellent” and “satisfied”); the the rate of poor response was 9.1% (Fig. 3a). We then compared combination therapy with PRP for melasma with treatment with PRP alone; the results showed that patients showed a higher subjective satisfaction with combination therapy with PRP than for treatment with PRP alone, with the combination of PRP + Q-switched laser receiving the highest satisfaction level, at 79.5% (Fig. 3b). Finally, we compared the subjective efficacy of microneedling and intradermal injection of PRP; this analysis showed that PRP microneedling therapy received a higher satisfaction rating and had a higher excellent efficacy rate than PRP + intradermal injection (34.5 vs. 26.3%) (Fig. 3c).
Fig. 3
Analysis of subjective evaluation. a Overall evaluation of the efficacy of PRP according to satisfaction level of subjects. b Difference in the proportion of subjective satisfaction ratings between PRP in combination therapy and PRP treatment alone. c Difference in the proportion of subjective satisfaction ratings between microneedling and intradermal injections of PRP
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Analysis of Adverse Reactions and Recurrence
No serious adverse events were reported in any of the included studies. Adverse reactions include local congestion, temporary erythema, hyperpigmentation and discoloration, all of which are few and generally mild. Observations at 3 months of follow-up showed that the average recurrence rate in the studies was about 5%. Two the studies [25, 28] mentioned a longer period of observation, all of which showed stronger benefits and did not affect our final conclusion.
Discussion
This meta-analysis of ten studies that involved 395 adults in clinical trials on PRP therapy, either in combination with other therapy or alone, showed a significant reduction in mMASI score from pre-treatment to post-treatment. The overall efficacy evaluation of PRP showed that patients or doctors had a high degree of satisfaction with the treatment of melasma by PRP. In addition, the PRP in combination with other therapies, microneedling in particular, received higher subjective satisfaction rating than PRP treatment alone and in combination with intradermal injection.
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Previous studies have shown that TGF-β1 in PRP can inhibit melanin synthesis by delaying activation of extracellular signal-regulated kinase [29]. Concomitantly, PDGF in PRP may also lead to increased skin volume (angiogenesis, collagen synthesis and extracellular matrix formation), resulting in reduced pigmentation and skin luster [14]. It has also been determined that the levels of leukocyte differentiation antigen-4, interleukin-17 and cyclooxygenase-2 are higher in patients with melasma than in normal control [30]. Thus, it can be speculated that the curative effect of PRP is not only related with pigment metabolism, but also with its multiple repair function, its antibacterial or anti-inflammatory effect and its skin imperceptible blood-vessel remodeling function, all of which play a role in the several major pathology and pathogenesis of melasma, namely impaired skin barrier function, inflammation [31], pigment metabolic disorders and vascular changes.
PRP is a relatively new strategy in the treatment of melasma. To our best knowledge, this paper is the first systematic review and meta-analysis of PRP for melasma. Our research has three main advantages: First, we have comprehensively and systematically evaluated and analyzed the role of PRP in the treatment of melasma by using publication bias, regression analysis, subgroup analysis and mean subjective evaluation methods. Second, we rigorously included articles, extracted, analyzed and grouped the data by two individuals, and selected the most common and reliable MASI scoring method [32] to achieve a relatively small heterogeneity among included studies. Third, the studies we included were all very recent studies, with publication dates concentrated between 2019 and 2021.
Among the studies included in our meta-analysis, there was one study [25] with greater heterogeneity compared with the other studies that achieved a more obvious efficacy with PRP microneedle injection. Microneedles provide a minimally invasive and painless route of drug delivery by forming microchannels in the skin to enhance the penetration of active substances. It has already been used to treat skin conditions, such as wrinkles, acne scarring and discoloration, as well as to help facial rejuvenation. Combined with the results of subjective efficacy evaluation, we have reason to believe that microneedling may be a good route of PRP administration.
In terms of improving treatment with PRP, we can try to improve or develop new administration routes of PRP to facilitate its clinical application. For example, a recent study reported that a single-hand synchronous application of PRP and microneedling by attaching a derma roller with a 5-ml pipette secured by a sterile micropore tape [33]. Another recent study [28] showed that PRP significantly outperformed tranexamic acid in treatment for melasma from week 4 through week 24, suggesting that PRP therapy may be superior to other procedures; however, more randomized controlled studies are needed to confirm this. In addition to regaining a more balanced and stable complexion, many patients with PRP also have improved skin quality, including wrinkle levels, elasticity and skin hydration [23, 34]. Therefore, it would be valuable to offer a more personalized combination therapy to patients who want to treat melasma and improve skin quality simultaneously. In terms of mechanism study, it is meaningful to study the upstream and downstream molecules interacting with TGF-β in melasma, such as transcription of activating protein-1, PAX3, p53, MITF, tyrosinase-related protein 1 and tyrosinase [35].
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There are a number of limitations associated with this meta-analysis. First, some of the included studies were of different duration and used treatment modalities of PRP. Second, not all of the included studies were strictly randomized controlled designs, which leads to reduced credibility in their results. Third, the MASI score of patients may be affected by a number of subjectively observed differences in the grading process. Fourth, due to insufficient data in the literature, we cannot determine the influence of melasma type or severity on the therapeutic effect of PRP.
Conclusions
Our research validated that PRP is a safe and efficient treatment for melasma. Used both alone and in combination therapy, PRP treatment achieved a significant reduction of the MASI score while only incurring mild adverse reactions. Based on subjective satisfaction evaluation of PRP, combining the use of microneedling with PRP may have better efficacy in melasma treatment than PRP alone or combined with intradermal injection. As PRP in the treatment of melasma is a novel concept, in order to provide new reliable methods for the treatment of melasma, more high-quality randomized controlled clinical studies are needed to verify our conclusions.
Acknowledgements
This work was supported by 1.3.5 Project for Disciplines of Excellence of West China Hospital of Sichuan University.
Funding
This work and the journal’s Rapid Service Fee was funded by 1.3.5 Project for Disciplines of Excellence of West China Hospital of Sichuan University.
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Authorship
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Authors’ Contributions
Li Li and Lingyun Zhao designed the experiment. Lingyun Zhao and Meng Hu extracted data. Lingyun Zhao and Meng Hu performed all statistical analyses. Runke Zhou and Qing Xiao participated in discussions to solve problems arising in the paper. Lidan Xiong and Li Li reviewed this article. All authors read and approved the final manuscript.
Disclosures
Lingyun Zhao, Meng Hu, Qing Xiao, Runke Zhou, Yu Li, Lidan Xiong, Li Li have nothing to disclose.
Compliance with Ethics Guidelines
This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.
Conflicts of Interest
The authors declared no potential conflicts of interest with respect to the research.
Data Availability
All data generated or analyzed during this study are included in this published article/as supplementary information files.
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