Targeting the dermis for melasma maintenance treatment (2024)

Melasma is a common acquired hyperpigmentary disorder and the treatment remains challenging¹. The gold standard treatment for melasma is Kligman’s formulation, which comprises hydroquinone, retinoid and corticosteroid². Recent studies have shown that oral administration of tranexamic acid (TA) has emerged as a promising treatment for melasma^3,4,5. Furthermore, the combination treatment was more effective than the topical agent alone in a randomized controlled trial⁶. However, relapse after discontinuation of these combination treatments is almost common and remains a major challenge in melasma treatment.

Melasma is recently regarded as one of the phenotypes of photoaging⁷. Evolving research indicates more heterogeneous pathomechanisms observed in melasma, including solar elastosis, increased vascularization, and an increased number of senescent fibroblasts, in addition to the inappropriate melanocyte activation^7,8. The continuous melanogenic signaling from the aging dermis, including photoaged fibroblasts or increased vasculatures, activates melanocytes and contributes to increased pigmentation in melasma⁹. Gene analysis studies, on aging pigmented skin, have identified the following novel melanogenesis-modulating factors from UV-radiated fibroblasts: secreted frizzled-related protein-2 (sFRP2)¹⁰, stromal-derived factor 1 (SDF1)¹¹, and growth differentiation factor-15 (GDF15)¹². These factors result in increased skin pigmentation and influence the development of pigmentary diseases associated with photoaging. Taken together, all these observations suggest that a dermal targeting strategy should be considered for melasma treatment apart from the direct controlling tyrosinase of melanocytes. In this prospective, split-face study, we investigated the maintenance effect of dermal targeting therapy using radiofrequency (RF) microneedling after conventional melasma treatment with oral TA and triple combination cream (TCC).

Subject demographics and flow diagram

This study has been registered in a Clinical Trial. (Clinical Trial registration number: NCT05710068, date of first registration: 02/02/2023) A total of fifteen female volunteers with facial melasma were analyzed. All the subjects had the Fitzpatrick skin type III (n = 5) or IV (n = 10). The mean age was 47.07years (range 37–62years) and the average duration of melasma was 9.73years. The baseline mMASI score was 5.02 ± 2.27 and L* values of the RF treated side and untreated side were 59.79 and 60.44, respectively (Table 1). All subjects received the conventional therapy of oral TA and TCC. The half face was randomly assigned for RF treatment (right side, n = 9; left side, n = 6). All subjects completed 2-month therapy and participated in the maintenance therapy with RF; however, four subjects withdrew during the maintenance therapy because of voluntary withdrawal of consent (n = 1) and COVID-19 pandemic (n = 3). Eventually, eleven subjects completed the study. The flow diagram of the study is shown in Fig.1.

Oral tranexamic acid combined with triple combination cream improves melasma

All the 15 subjects showed marked improvement after 2-month conventional treatment. (Fig.2a–e) The mMASI score significantly decreased from 5.02 ± 2.27 to 1.80 ± 1.38 (p < 0.01) with 64.1% reduction on average. Both L* values of the RF treated and untreated side increased from 59.79 ± 1.79 and 60.44 ± 1.91 to 62.86 ± 1.74 and 62.55 ± 2.03, respectively (3.07 vs. 2.11, p = 0.40). From the perspective of the synergistic effect of RF, there was no significant difference in the RF group in addition to the combination treatment of oral TA and TCC, although RF group showed better improvement. There were no significant side effects including erythema or irritation.

The continuous adjuvant RF treatment helps maintaining the treatment effect of conventional therapy

After discontinuation of conventional therapy, a total of eleven subjects maintained the half face RF every month for 6months. The Δ L* (mean change of L* value from the baseline) of the untreated side decreased significantly from the first month after cessation of conventional therapy. The mean L* value reached to the baseline in 6months (Figs. 2c,f, 3). In contrast, the RF treated side helped maintaining the treatment effect after cessation of the 2-month previous treatment, i.e. Δ L* on the RF treated side maintained above 2.7 through the study duration. Mild erythema and pain were reported on the area that were treated with RF therapy but resolved in 30min. Other serious adverse effects such as bleeding, infection, postinflammatory hyperpigmentation and scarring were not reported during the study period.

The present study showed that dermal targeting therapy using RF microneedling can prevent the relapse of previously improved melasma lesions. In the untreated side, seven subjects (63.6%) returned to the baseline state at 6months follow-up after discontinuation of the conventional treatment, whereas RF treated side maintained the improvement of melasma, suggesting the protective effect of RF in melasma relapse. It should be noted that in this study, the subjects were enrolled at the end of winter season and followed up after summer to remove confounding factor of spontaneous improvement of melasma during autumn and winter. Indeed, the adjuvant RF treatment helped maintaining the efficacy, even though they went through 1 summer. However, the microneedling RF in addition to the conventional therapy did not show superiority to the conventional therapy alone, although former showed better improvement in the Δ L* value. The reason is likely because the effects of oral TA and TCC are already quite substantial. Indeed, a previous report has shown that the microneedling RF has a synergistic effect on the aging-associated pigmentary diseases in combination with the conventional Q-switched ND:YAG laser¹³.

The dermal targeting therapy involves energy-based devices such as RF, pulsed-dye laser and intense pulsed light to induce dermal rejuvenation¹⁴. In this study, the microneedle RF device was chosen to manipulate only dermal structures, in which the microneedles generate thermal coagulation columns in the dermis, not in the epidermis¹⁵. The RF treatment induced rejuvenation of aging dermis in melasma and senile lentigo, which subsequently makes it possible to resolve inappropriate melanin production from the dermis^11,16. A nonspecific reduction in p16^INK4A positive senescent fibroblasts and the stimulation of procollagen production after RF treatment were shown to contribute to a decrease in epidermal pigmentation in melasma and senile lentigo^11,16. The beneficial effect of pulsed dye laser for melasma was also previously shown¹⁷. The reduction of dermal vasculatures of melasma appeared to improve the treatment effect of topical TCC and also prevented the relapse of melasma^17,18. This effect was thought to be related in reduction of melanocyte activation signaling from endothelial cells such as endothelin-1 and stem cell factor^19,20. Taken together, it is speculated that the dermal targeting treatment might be beneficial for long-term treatment of melasma. However, particular attention should be given to the possibility of worsening melasma due to epidermal heating, especially in non-insulated RF therapy.

Another interesting finding of our study include that the effectiveness of oral TA combined with TCC for melasma treatment was confirmed. All the subjects showed marked improvement of mMASI (64.1% reduction) after 2-month treatment that is comparable with previous studies. There was 65.45% improvement in mMASI at week 8²¹ and 62% improvement at week 20²² in Mexican study, 51% improvement in MASI at week 12 in Iran study and 87.9% improvement in MASI at week 8 in Indian study²³ after administering oral TA and TCC. The efficacy of combination treatment is superior to the monotherapy of oral TA, i.e. oral TA alone showed 49% reduction in mMASI score for 3-month treatment⁵. Moreover, no serious adverse events were reported in the conventional treatment^5,21,23,24. Taken together, the combination therapy of oral TA and TCC might be considered as a standard treatment of melasma. However, relapse after cessation of the treatments is remained as a major challenge. In the presented study, we also found that the efficacy gradually disappears after discontinuation in 1month and all returned to the baseline in 6months. This recurrence rate is similar to the previous studies; most patients who received oral TA 500mg daily experienced relapse in 6weeks post discontinuation²⁵. Relapse rate after ceasing oral TA was reported 72% within 2months²⁶ and mean MASI was rebound to 77.4% compared to baseline within 3months after discontinuation of oral TA and topical hydroquinone²⁷. Therefore, these finding emphasize the beneficial role of dermal targeting therapy for the melasma treatment.

Our study has some limitations; there was a small sample size, and all the subjects were female with similar ethnic backgrounds. However, the strength of this study is the first study investigating the long-term maintenance effects of dermal targeting therapy using microneedling RF for melasma treatment.

In conclusion, the microneedling RF therapy appears to be beneficial in combination with the conventional therapy of melasma, suggesting the protective effect of dermal targeting therapy in melasma relapse.

Study design

This was a randomized, split-face clinical trial conducted at the department of dermatology in a single tertiary center (Ajou University Hospital, Seoul, Korea) from December, 2021 to August, 2022. This study was divided into two stages; first 2months, oral TA and TCC as well as the half face RF treatment were given. After the improvement of melasma, oral TA and TCC were discontinued, but the RF microneedling continued on half of the face for an additional 6months.

Subjects

Melasma was clinically diagnosed by three dermatologists (J.C. Kim, Y.J. Park, H.Y. Kang). Subjects who had undergone prior aesthetic medical procedures or used topical depigmenting agents in three months prior to the study and were pregnant or lactating were all excluded. A total of 20 volunteers were screened and five subjects failed screening; four were diagnosed as solar lentigo and one had a history of laser treatment in one month. As a result, fifteen female volunteers with facial melasma were enrolled in the study. Four subjects withdrew during the study because of 1 voluntary withdrawal of consent and 3 COVID-19 pandemics. Eleven subjects finally completed the 8-month study.

Intervention

For the first 2months, the subjects were instructed to take oral TA 250mg twice daily and apply TCC composed of 5% hydroquinone, 0.003% tretinoin, and 1% hydrocortisone (Melanon cream, DONG-A ST, Korea) to the entire face once a day for 8weeks. This regimen was referred to as “conventional therapy” in this study. Concurrently, randomly assigned half face was treated using a pulsed-type RF device in bipolar mode with 25 non-insulated microneedles (Sylfirm X™, VIOL, Korea) every 2weeks. Parameters were set pulsed-wave mode (PW2) at level 4–6 targeting mild erythema with a penetration depth of 0.3mm for two passes and 0.8mm for one pass. After discontinuation of the conventional therapy, the half face RF therapy was maintained every month for 6months. This regimen was referred to as “maintenance therapy”. (Fig.4.)

All subjects received sunscreens (Uvidea Anthelios, LA ROCHE-POSAY, Paris) and barrier repair creams (Zeroid intensive cream, NEOPHARM, Korea) during the study. All the treatments were performed by a single experienced dermatologist. Standard clinical photographs were taken every month with a digital camera (Nikon D5600, Japan) and a pigment imaging tool (JANUS Pro Hybrid®, PIE Co., Ltd., Korea).

Treatment outcomes

Modified melasma area severity index (mMASI) score²⁸ and L* value measured by a chromameter were collected monthly. The mMASI score was assessed by two independent dermatologists (H.J. Han and H.Y. Kang) using digital photographs every month as follows: forehead, 0.15 × D × A, malar, 0.30 × D × A, chin, 0.05 × D × A; A, area involved; D, darkness. Skin pigmentation levels were measured on both sides of the face respectively using a chromameter (CR-300; Minolta, Japan), and values of lightness denoted by L* were recorded every month. The measured location was recorded to compare the lightness of the same spot. The Δ L* (mean change of L* value from the baseline) of the RF treated side and untreated side were calculated respectively every month. Adverse effects were collected at each treatment session and follow-up visit.

Statistical analysis

Data were evaluated by two-way repeated measures analysis of variance (ANOVA) to compare the trends of L* values. The result was considered statistically significant when the p value was less than 0.05 and SPSS software (IBM SPSS Statistics for Windows, Version 25.0. Armonk, NY) was used to analyze the data.

Ethical statement

This study was approved by the institutional review board of Ajou University Hospital (IRB number: AJIRB-DEV-INT-21-133). The protocol was initiated following written informed consent in adherence to the principles of Declaration of Helsinki and regulations for Good Clinical Practice. (Clinical Trial registration number: NCT05710068, date of first registration: 02/02/2023).

GDF15:

Growth differentiation factor-15

mMASI:

Modified melasma area severity index

RF:

Radiofrequency

SDF1:

Stromal-derived factor 1

sFRP2:

Secreted frizzled-related protein-2

TA:

Tranexamic acid

TCC:

Triple combination cream

Authors and Affiliations

1. Department of Dermatology, Ajou University Hospital, 164, World Cup-Ro, Yeongtong-Gu, Suwon-Si, Gyeonggi-Do, 16499, South Korea

   Hee Jeong Han,Jin Cheol Kim,Young Joon Park&Hee Young Kang

Contributions

Author H.J.H. and J.C.K. contributed equally to this work. Conceptualization and methodology: H.Y.K., Y.J.P. Data curation and formal analysis: H.J.H. Funding acquisition: this study was funded by VIOL Inc. Project administration: All authors. Supervision: H.Y.K. Writing: H.J.H. and J.C.K.

Corresponding author

Correspondence to Hee Young Kang.

Competing interests

The authors declare no competing interests.

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions