Next Article in Journal
Intramuscular Botulinum Toxin for Complex Regional Pain Syndrome: A Narrative Review of Published Cases
Previous Article in Journal
Recent Advancements in Lateral Flow Assays for Food Mycotoxin Detection: A Review of Nanoparticle-Based Methods and Innovations
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Efficacy and Safety of Letibotulinum Toxin A for the Treatment of Melasma in Two Different Dilutions: A Randomized Double-Blind Split-Face Study

by
Juthapa Pongklaokam
1,
Woraphong Manuskiatti
1,
Rungsima Wanitphakdeedecha
1,
Pitchaya Maneeprasopchoke
1,
Panwadee Thongjaroensirikul
1,
Yanin Nokdhes
1,
Rona Maria R. Abad-Constantino
2,
Woramate Bhorntarakcharoen
1,
Sariya Sittiwanaruk
1 and
Thanya Techapichetvanich
1,*
1
Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, 2 Wanglang Road, Bangkok Noi, Bangkok 10700, Thailand
2
Department of Dermatology, Research Institute for Tropical Medicine, 9002 Research, Mutinlupa 1781, Philippines
*
Author to whom correspondence should be addressed.
Toxins 2025, 17(7), 349; https://doi.org/10.3390/toxins17070349
Submission received: 11 June 2025 / Revised: 1 July 2025 / Accepted: 8 July 2025 / Published: 11 July 2025
(This article belongs to the Special Issue The Evolving Role of Botulinum Toxin in Clinical Therapeutics)

Abstract

Background: Melasma is an acquired hyperpigmentation disorder with multifactorial etiologies and limited response to conventional therapies. Recent evidence suggests that Botulinum Toxin A (BoNT-A) may modulate ultraviolet (UV)-induced pigmentation and offer therapeutic benefits. Objective: We sought to evaluate the efficacy and safety of two intradermal dilutions of Letibotulinum toxin A (LetiBoNT-A) in Thai patients with melasma. Methods: In this randomized, double-blind, split-face study, 30 participants aged 32–62 years received a single intradermal injection of LetiBoNT-A, with 20 units administered per cheek. A 1:5 dilution was injected on one side of the face, and a 1:10 dilution was injected on the contralateral side. Outcomes were evaluated over a 6-month period using the Hemi-modified Melasma Area and Severity Index (Hemi-mMASI), VISIA® brown spot analysis, and quantitative assessments of skin texture. Results: Both dilutions significantly improved Hemi-mMASI scores (1:5, p = 0.043; 1:10, p = 0.002) and brown spots (1:5, p = 0.002; 1:10, p < 0.001). The 1:10 dilution showed earlier and more sustained improvements. Subgroup analysis revealed greater reductions in Hemi-mMASI scores among patients with telangiectatic melasma, particularly with the 1:10 dilution, though they were not statistically significant. Additionally, the 1:10 dilution significantly reduced pore volume, pore area, and sebum levels. One case of transient facial asymmetry was reported with the 1:5 dilution. Conclusions: LetiBoNT-A is a safe and effective adjunct in melasma treatment. The 1:10 dilution offered superior clinical outcomes.
Key Contribution: This study is the first to directly compare two intradermal dilutions of Letibotulinum toxin A (1:5 vs. 1:10) for melasma treatment. The findings indicate that the lower concentration (1:10), with greater diffusion, provides earlier and more sustained clinical improvement in pigmentation, skin texture, and sebum control, highlighting its superior efficacy and safety profile.

1. Introduction

Melasma is an acquired hyperpigmentation disorder presenting as brown to gray/brown facial patches, commonly on sun-exposed areas. It is classified as epidermal, dermal, mixed, or indeterminate [1].
The condition is driven by hyperactive melanocytes and influenced by factors such as UV exposure, hormonal changes, genetics, and medications. Recent studies also implicate mast cell activity, solar elastosis, basement membrane disruption, and vascular changes [2]. UV radiation plays a central role by increasing tyrosinase activity and upregulating pigment-inducing mediators such as VEGF [3,4,5].
Melasma treatment involves sun protection and pigment-suppressing therapies. Topical agents, including hydroquinone, triple-combination creams, azelaic acid, and chemical peels, target melanin synthesis and inflammation [6]. Tranexamic acid, given orally, topically, or intradermally, also acts on vascular and pigment pathways [2]. Laser- and light-based therapies (e.g., Q-switched, picosecond, and fractional lasers) are options for refractory cases but carry risks such as PIH and ochronosis. Oral tranexamic acid may also increase thrombotic risk [1,2,6].
  • Botulinum Toxin and Skin Pigmentation
Botulinum toxin A (BoNT-A), derived from Clostridium botulinum, inhibits acetylcholine release at neuromuscular junctions, causing temporary muscle paralysis [7,8,9]. Of the known serotypes (A–G), only BoNT-A and BoNT-B are used clinically, with BoNT-A being the most widely applied due to its efficacy and duration [10,11,12].
Interest in BoNT-A’s pigment-modulating effects stemmed from reports of localized hypopigmentation following periocular injections in patients with facial spasms [13]. Subsequent in vitro studies demonstrated that BoNT-A pretreatment reduced melanin content, tyrosinase activity, and dendrite formation in UVB-irradiated melanocytes and keratinocytes [14]. Animal studies confirmed reduced pigmentation, tyrosinase activity, and levels of inflammatory mediators such as bFGF, IL-1α, and PGE2 [14].
Clinical studies have reported decreased melanin levels in BoNT-A-treated skin, with improved brightness and reduced pigmentation in both pre- and post-UVB exposure models [15,16,17]. However, one study found no significant effect, suggesting that timing and dosage may influence outcomes [18].
Beyond pigment modulation, BoNT-A improves skin texture and reduces lentigines, pore size, and telangiectasia [19,20]. Its antiangiogenic effects, mediated by VEGF downregulation [21], further support its application in vascular conditions such as rosacea [22,23,24,25,26,27,28,29,30,31,32]. Collectively, these findings suggest BoNT-A as a potential treatment for melasma, addressing both pigmentary and vascular components.
  • Melasma Clinical Research
While in vitro studies support the antimelanogenic and vascular-modulating effects of botulinum toxin A (BoNT-A), clinical evidence in relation to melasma remains limited. A split-face study in Thailand involving twelve patients with mixed-type melasma demonstrated that intradermal Abobotulinum toxin A (AboBoNT-A) injections in one cheek (0.1 mL per point, spaced 1 cm apart; 2.5 units/cm2) led to significant reductions in H-mMASI scores and melanin index on the treated side across all follow-up visits (2, 4, 8, and 12 weeks), while the untreated side showed no change [33].
A more recent randomized, double-blind, split-face study reinforced these findings. Twelve patients received AboBoNT-A at 66.7 units/mL via 2 mm intradermal wheals spaced 2 mm apart. At 3 months, significant improvements were observed in both the Melasma Area and Severity Index (MASI) and Physician Global Assessment (PGA) scores.
Complementary in vitro studies using UVA-irradiated B16F10 melanoma cells confirmed that BoNT-A reduced melanin content and tyrosinase activity in a dose-dependent manner without cytotoxic effects [34].
These clinical and laboratory findings support BoNT-A as a promising treatment for melasma, acting through inhibition of melanogenesis and modulation of inflammatory and vascular pathways.
  • Significance of this Study
Botulinum toxin shows promise in treating melasma by targeting both pigmentation and vascular components. However, melasma remains difficult to manage due to its multifactorial pathogenesis, recurrence, and variable treatment outcomes. Existing studies on BoNT-A are limited by small sample sizes and lack standardized dilution protocols, and Letibotulinum toxin A (LetiBoNT-A) has not yet been evaluated in this context.
In this study, we aimed to compare the efficacy and safety of two intradermal LetiBoNT-A dilutions (1:5 and 1:10) using a randomized, double-blind, split-face design. Secondary outcomes included changes in pore size, sebum production, and facial erythema. Subgroup analysis was conducted to assess responses between telangiectatic and non-telangiectatic melasma types. The findings may help establish standardized protocols for BoNT-A use in melasma treatment.

2. Results

A total of 31 participants were enrolled, but 1 withdrew due to scheduling conflicts. Thus, 30 completed this study and were included in the final analysis.

2.1. Demographic Data

The mean age was 47 ± 6.6 years (range: 32–62), with most participants being female (96.67%) and having Fitzpatrick skin types IV (70%) or V (16.67%). Melasma was categorized as non-telangiectatic (53.33%) and telangiectatic (46.67%). Baseline Hemi-mMASI scores were higher in the telangiectatic group across both dilutions. Pain scores were similar between dilutions (1:5 = 5.13 ± 2.29; 1:10 = 5.23 ± 2.21) (Table 1).

2.2. Outcomes

Primary outcomes:
  • Hemi-modified Melasma Area and Severity Index (Hemi-mMASI);
  • Brown spot count via VISIA®;
  • Adverse events.
Secondary outcomes:
  • Red area via VISIA®;
  • Sebum level (Sebumeter®);
  • Mean pore area and volume (Antera 3D®);
  • Subjective evaluation by dermatologists;
    (Investigator Global Aesthetic Improvement Scale (IGAS));
  • Subjective evaluation by participants (Patient Global Assessment (PGA)).

2.2.1. Mean Hemi-MASI Modified Melasma Area and Severity Index (Hemi-mMASI) in the Melasma Area

The subjective assessment of Hemi-mMASI scores by two blinded dermatologists revealed significant improvements in melasma severity for both 1:5 and 1:10 dilutions over six months. Statistically significant reductions were noted at specific follow-up points: 2 weeks for the 1:10 dilution (p = 0.006), and 6 months for both dilutions (1:5 dilution: p = 0.043; 1:10 dilution: p = 0.002). The 1:10 dilution showed a more consistent statistical significance reduction in Hemi-mMASI score from baseline compared to the 1:5 dilution (Table 2, Figure 1).
At the 6-month follow-up, the 1:5 dilution resulted in a 14% improvement in Hemi-mMASI scores (from 4.38 ± 1.66 at baseline to 3.78 ± 1.49 at 6 months, p = 0.043), while the 1:10 dilution led to a 21% improvement in Hemi-mMASI scores (from 4.47 ± 1.63 at baseline to 3.53 ± 1.32 at 6 months, p = 0.002) (Table 2).
However, when comparing the two concentrations directly, no significant differences were found, indicating that both dilutions are similarly effective (Table 2). The 1:10 dilution demonstrated faster and more consistent improvements, with greater reductions in pigmentation at each time point as soon as 2 weeks after injections (p = 0.006) and sustainable for 4 and 6 months (p = 0.002). Therefore, while both dilutions were effective, the 1:10 dilution provided faster and generally more significant improvements in melasma treatment (Figure 1).
Figure 2 presents an example of clinical pictures assessed by the blinded dermatologists, demonstrating improvements aligned with the Hemi-mMASI scores. The 1:10 dilution exhibited notable reduction in pigmentation as early as the 2-week follow-up and sustained continuous improvement by 6 months, revealing even more substantial alterations relative to the baseline. Conversely, the 1:5 dilution exhibited less pronounced enhancements, yielding somewhat less impressive outcomes, but nonetheless indicated significant improvement at 6 months relative to the baseline.

2.2.2. Brown Spots and Red Areas Assessed with VISIA® in the Melasma Area

The objective assessment of brown spots and red areas with VISIA® is shown in Table 3 and Figure 3. Over a six-month period, VISIA® complexion analysis demonstrated substantial decreases in brown spots for both dilutions (1:5 and 1:10). Improvements were found to be statistically significant as early as from one month (p = 0.017 for 1:5; p = 0.007 for 1:10) to six months (p = 0.002 for 1:5; p < 0.001 for 1:10). For the red area, only the 1:10 dilution shows a significant reduction at 6 months (p = 0.032), while this was not seen in the 1:5 dilution.

2.2.3. Subgroup Analysis

A subgroup analysis was performed to evaluate treatment responses between two melasma subtypes: non-telangiectatic melasma (pigment-only type) and telangiectatic melasma (characterized by the presence of visible vascular components). Both groups demonstrated reductions in Hemi-mMASI scores across all follow-up time points for both the 1:5 and 1:10 dilutions. However, no statistically significant differences were observed between the two subtypes at any time point or across any of the measured parameters, including mean change in Hemi-mMASI scores and brown spot counts.
At 6 months (Figure 4 and Figure 5), the telangiectatic melasma group generally showed greater reductions in Hemi-mMASI scores from baseline, particularly with the 1:10 dilution, although these changes did not reach statistical significance. This trend was less apparent with the 1:5 dilution. Despite the absence of statistical differences, the numerical improvement in the telangiectatic group may suggest a slightly enhanced clinical response, warranting further investigation in larger studies.
These findings suggest that the efficacy of LetiBoNT-A was comparable between melasma subtypes, with both pigment-dominant and vascular-associated forms responding similarly to treatment.

2.2.4. Sebum Level from Measurement with Sebumeter® in the Blemish Area

The Sebumeter® assessment revealed differences in sebum levels between the 1:5 and 1:10 dilutions. For the 1:10 dilution, a statistically significant reduction in sebum levels was observed at the 1-month follow-up (p = 0.037) compared to the baseline over time (Table S1).

2.2.5. Mean Pore Area and Mean Pore Volume Based on Antera 3D®

This study evaluated the mean pore volume and area using Antera® 3D (Miravex Ltd., Dublin, Ireland). The results revealed a significant reduction in mean pore volume and area for the 1:10 dilution at the 2-week and 1-month follow-ups (p < 0.05), compared to the baseline. No significant differences were observed beyond the 2-month follow-up for either dilution, as shown in Table S2 and Figure S1.

2.2.6. Subjective Evaluation of Treatment Results from Photographs by Two Dermatologists

Overall, the majority of investigators were satisfied with the treatment outcome in both dilutions (Figure S2). This is consistent with the treatment outcome from both Hemi-mMASI and brown spots with VISIA® imaging (Canfield Scientific, Inc., Parsippany, NJ, USA). For dilution 1:5, the highest improvement was observed at 2 months, with 29% of patients reporting marked improvement. At 6 months, the results remained consistent, with 28% showing mild to moderate improvement and 24% experiencing marked improvement. For dilution 1:10, moderate improvement peaked at 2 months (32%), while marked improvement steadily increased, reaching 23% at 6 months. Overall, both dilutions demonstrated sustained improvement, with dilution 1:10 showing slightly greater effectiveness at the 6-month follow-up.

2.2.7. Subjective Evaluation of Treatment Results by Volunteers

Both dilutions show improvement over time, with a higher percentage of patients reporting 76–100% improvement at 6 months (30%) (Figure 6).

2.3. Adverse Events

Redness and dryness were reported by one patient two weeks after receiving the 1:10 dilution of Letibotulinum toxin A. Additionally, one patient experienced a transient asymmetrical grimace one month after treatment with the 1:5 dilution. Considering the overall efficacy and adverse event profile, the 1:10 dilution may be preferable, as it was not associated with any muscle-related complications and demonstrated a more favorable safety profile.

3. Discussion

This study demonstrates that both 1:5 and 1:10 dilutions of intradermal Letibotulinum toxin A significantly improve melasma severity. Improvements were observed across objective and subjective measures, including Hemi-mMASI scores, VISIA® brown spot analysis, and both investigator- and patient-reported outcomes. Notably, the 1:10 dilution consistently yielded stronger statistical significance and more uniform improvements across endpoints, particularly in reducing pigmentation, brown spots, sebum levels, mean pore volume, and pore area. Importantly, no serious adverse events were reported in either group.
The primary aim of our study was to investigate the clinical effects of two different dilutions (1:5 and 1:10) utilizing a single commercially available product. LetiBoNT-A was selected as the study agent due to its increasing clinical utilization in Asia, including Thailand, as well as its established safety profile in aesthetic applications.
Hemi-mMASI scores improved significantly over the 6-month period with both dilutions (1:5, p = 0.043; 1:10, p = 0.002), while brown spot counts also significantly declined (1:5, p = 0.002; 1:10, p < 0.001). The 1:10 dilution showed statistically significant improvement as early as two weeks (p = 0.006), indicating a faster onset of action. Despite these trends, no statistically significant differences were found between dilutions at any time point, suggesting that both concentrations are clinically effective, though the 1:10 dilution may offer more rapid and sustained outcomes.
In terms of pore-related parameters, the 1:10 dilution demonstrated a significant decrease in mean pore volume and area at 2 and 4 weeks (p < 0.05). However, these improvements were not maintained beyond 2 months, suggesting the potential need for booster or maintenance treatments to prolong the effects. Sebum production also decreased significantly at 1 month with the 1:10 dilution (p = 0.037), reinforcing its efficacy in improving overall skin texture and oiliness.
It is important to recognize that the mechanisms of action of botulinum toxin type A (BoNT-A) on muscle, melanocytes, and sebaceous glands are mechanistically distinct. Therefore, the duration of BoNT-A’s effects in melasma cannot be presumed to parallel its duration in muscle relaxation or sebum suppression.
In skeletal muscle, BoNT-A acts by inhibiting acetylcholine (ACh) release at the neuromuscular junction, thereby preventing its binding to postsynaptic receptors and leading to functional denervation and muscle relaxation. This effect typically persists for 4–6 months, corresponding to the time required for axonal sprouting and synaptic reformation.
In contrast, cutaneous tissues express a non-neuronal cholinergic system (NNCS), whereby cells such as sebocytes, keratinocytes, and melanocytes synthesize and respond to ACh independent of neuronal input. Within sebaceous glands, ACh has been implicated in regulating sebocyte proliferation and sebum production. BoNT-A may attenuate sebum secretion by interfering with this cholinergic signaling; however, the in vivo response of human sebaceous glands to cholinergic blockade remains incompletely characterized. Notably, it is unclear whether chronic ACh exposure or receptor desensitization occurs with time. In our study, the reduction in sebum production following BoNT-A injection was significant but transient, persisting for approximately one month—considerably shorter than the duration typically observed in muscular effects.
Melanocytes, the primary pigment-producing cells, also express ACh receptors, suggesting that BoNT-A may modulate melanogenesis via cholinergic pathways. In vitro studies have demonstrated that BoNT-A reduces melanocyte dendricity and intracellular melanin content. In vivo treatment with BoNT-A has been associated with decreased pigmentation and reductions in DOPA-positive melanocytes, tyrosinase activity, melanin levels, basic fibroblast growth factor, interleukin-1 alpha, and prostaglandin E2. These data suggest a multifactorial inhibitory effect of BoNT-A on pigment production and inflammation [35].
Given these mechanistic distinctions, the duration and consistency of BoNT-A’s effects in melasma may differ from its muscular and sebaceous applications. Notably, the suppressive effects on melanogenesis and vascular proliferation, central to melasma pathophysiology, may be more durable due to broader immunomodulatory and anti-inflammatory actions. However, further studies are needed to elucidate the longevity of these effects and their underlying molecular mechanisms.
Subgroup analysis between melasma subtypes revealed that both telangiectatic and non-telangiectatic melasma improved in response to treatment. The telangiectatic group showed greater improvements with the 1:10 dilution, especially at 4 and 6 months, indicating potential long-term benefits in this subgroup. Telangiectatic melasma, which involves both pigmentary and vascular abnormalities, may particularly benefit from BoNT-A’s dual action on melanogenesis [14,16,18] and vascular modulation [21,36]. Studies using Dynamic Optical Coherence Tomography (D-OCT) have shown increased papillary and reticular dermal blood flow in melasma, especially within telangiectatic lesions [37]. The enhanced diffusion of the 1:10 dilution may allow for broader dermal penetration, potentially reaching vascular targets more effectively. These findings highlight the importance of considering melasma subtype and dilution characteristics when designing treatment protocols.
Although our study suggests that the 1:10 dilution offers not only greater efficacy but also an earlier onset of visible improvement, making it a promising option for patients seeking faster results, the question of treatment longevity remains important. Both dilutions demonstrated sustained improvement over the 6-month follow-up period, with the 1:10 dilution showing greater consistency across time points. For patients who achieve moderate improvement (51–75%) or those with telangiectatic melasma, additional treatment sessions may offer incremental benefits. Given the favorable safety profile observed, incorporating maintenance treatments at extended intervals (e.g., every 3–4 months) could be a practical strategy to maintain and enhance therapeutic outcomes.
Moreover, there was an improvement in adjacent untreated areas, such as the upper eyelids, as shown in Figure 2. BoNT-A may influence pigmentation beyond the injection site via indirect mechanisms. These include modulation of toll-like receptor 2 (TLR2)-mediated inflammation [38], cholinergic vasodilation [39,40], and neuropeptide signaling, particularly involving calcitonin gene-related peptide (CGRP) and substance P (SP). CGRP has been shown to upregulate NK-1R, which cooperates with SP to inhibit tyrosinase activity and melanin synthesis in melanocytes—even outside directly treated regions [41,42].
While previous studies have indicated that factors such as injection volume, concentration, and dosage play a significant role in toxin diffusion, whereas molecular weight and the presence of complexing proteins appear to have minimal impact, our findings may not be extrapolated to other BoNT-A products. Both preclinical and clinical data suggest that botulinum toxin formulations are not interchangeable, with some products demonstrating greater diffusion properties and higher rates of diffusion-related adverse events. This variability is attributed to the fact that each botulinum toxin product constitutes a unique pharmacological entity. Accordingly, a comprehensive understanding of the individual characteristics and diffusion profiles of different BoNT-A formulations is essential for accurately assessing their clinical effectiveness and for minimizing the risk of unintended diffusion and associated adverse effects [43,44,45].
Adverse events were minimal. One patient in the 1:10 group reported mild redness and dryness, which resolved spontaneously. One case of transient facial asymmetry occurred in the 1:5 group, which resolved without intervention. The absence of muscle-related side effects in the 1:10 group supports its favorable safety profile, particularly in aesthetic applications where symmetry is essential. Lastly, although our study demonstrated minimal side effects, it is important to note that injections were limited to the cheek area. In cases where melasma is presented more diffusely, caution should be exercised. It would be valuable to define clear safety margins, particularly by avoiding the upper and medial areas near the periorbital region, the nasolabial fold, and the corners of the mouth, to minimize the risk of unintended effects on facial muscles.

4. Conclusions

The 1:5 and 1:10 dilutions of Letibotulinum toxin A significantly improved melasma severity after a single treatment. Compared to the 1:5 dilution, the 1:10 dilution provided faster and more sustained improvements in pigmentation, skin texture, and sebum production, making it the better option for patients desiring quicker results. Although not statistically significant, the telangiectatic melasma subgroup showed greater proportional improvement with the 1:10 dilution at 6 months. Additionally, the 1:10 dilution may reduce the risk of asymmetry and offers a safer profile, supporting its potential for use in ongoing or combination therapies.

5. Materials and Methods

5.1. Study Design and Patient Selection

This was a randomized double-blind split-face clinical trial conducted at a university hospital in Bangkok, Thailand. A total of 30 Thai participants (29 women, 1 man; mean age 47 ± 6.6 years; range 32–62) with epidermal or mixed-type melasma and Fitzpatrick skin types III–V were enrolled. This study aimed to compare the efficacy and safety of two intradermal dilutions of Letibotulinum toxin A (LetiBoNT-A) for melasma treatment. The trial was registered in the Thai Clinical Trials Registry (TCTR20250208002; https://www.thaiclinicaltrials.org/show/TCTR20250208002, accessed on 1 July 2025), with the first submission date on 12 January 2025. The sample size was estimated based on a prior study [33], which showed a reduction in melanin index after 8 weeks of intradermal botulinum toxin A. With a two-sided alpha of 0.05 and 80% power, 26 participants were required. Accounting for a 15% dropout, the target sample size was 30. No changes were made after the trial commenced.
Recruitment of follow-up participants was conducted between January and June 2024, with follow-up completed by December 2024. One participant was lost to follow-up due to scheduling conflicts. Thus, data from 30 participants were included in the final analysis. For those unable to attend in-person visits, the follow-up data were collected via telephone interviews [46] (Figure S3).
Key exclusion criteria included pregnancy, breastfeeding, recent BoNT-A or aesthetic procedures (within 6–12 months), autoimmune disease, coagulation disorders, systemic or topical pigment-modulating therapies within 1–6 months, recent facial laser treatments, and use of photosensitizing medications. Participants engaging in regular unprotected sun exposure were also excluded. This study was conducted according to the guidelines of the Declaration of Helsinki and was approved by the Ethics Committee of the Siriraj Institutional Review Board (si 457/2023) on 9 June 2023. Informed consent was obtained from all participants.

5.2. Treatment Preparation, Area Selection

LetiBoNT-A (Aestox®, Hugel Inc., Chuncheon, South Korea) was reconstituted into two concentrations: 1:5 dilution, 100 units in 5 mL normal saline (20 U/mL); and 1:10 dilution, 100 units in 10 mL normal saline (10 U/mL). Each side of the face was randomly assigned to receive one of the two dilutions using a computer-generated sequence (www.randomization.com, accessed on 1 July 2025). Injections were administered intradermally using a 30 G needle at a 20–30° angle over a standardized 40 cm2 cheek area (8 × 5 cm). A total of 20 units was injected per side at 0.5 units/cm2. The 1:5 dilution was injected at 0.025 mL/cm2, and the 1:10 dilution at 0.05 mL/cm2 (Figure 7). Topical anesthetic EMLA® (AstraZeneca AB, Södertälje, Sweden) was applied 40–60 min before treatment.
To avoid asymmetries, it is essential to perform strictly intradermal injections while avoiding the zygomaticus minor and major muscles, both ideally located 1 cm from the orbital rim. The risorius muscle, important for lateral lip movement, should be injected approximately 2 mm lateral to the commissure to prevent uneven expression. Additionally, injections into the Levator Labii Superioris (LLS) and Levator Labii Superioris Alaeque Nasi (LLSAN) should be made 2 mm lateral to the alar-facial groove at the level of the nasal passage, ensuring proper muscle function and aesthetic outcomes [47,48,49,50].
The allocation sequence was concealed from the treating physician. Syringes were pre-filled and labeled by an independent assistant to ensure blinding. The injector, participants, and outcome assessors were blinded to treatment allocation.

5.3. Post-Treatment Care

Following treatment, the participants received ice compresses for 15–20 min. The participants were instructed to apply the provided broad-spectrum sunscreen daily and avoid any additional aesthetic procedures throughout the 6-month follow-up period. The use of other pigment-targeting therapies—including topical bleaching agents (e.g., alpha arbutin, AHA, vitamin C, azelaic acid, kojic acid, hydroquinone, and tretinoin), oral medications, injectable treatments, laser therapies, or energy-based devices—was strictly prohibited in the treated area for the duration of this study and until the final follow-up visit.

5.4. Objective Evaluation

For objective evaluations, standardized facial photographs were taken at baseline and all follow-up visits (2 weeks, 1, 2, 3, and 6 months) from five angles (90°, 45°, 0°, −45°, and −90°) under identical lighting and settings. Blinded dermatologists assessed clinical improvement using the Hemi-modified Melasma Area and Severity Index (Hemi-mMASI), calculated as follows:
Hemi-mMASI = 0.15 × A(F) × P(F) + 0.3 × A(Malar) × P(Malar) + 0.05 × A(Mandibular) × P(Mandibular)
where area (A) and pigmentation (P) are scored using established scales (0–6 and 0–4, respectively) [51].
Additional objective assessments included VISIA® (Canfield Scientific, Inc., USA) for brown and red spot analysis, Antera 3D® (Miravex, Dublin 2, Ireland) for mean pore area and volume over 5 cm2, and Sebumeter® SM815 (Courage + Khazaka electronic GmbH, Köln Germany) to measure sebum levels after 20 min of acclimatization at 25 °C and 70% humidity.

5.5. Subjective Evaluation

Subjective clinical improvement was evaluated using the Investigator Global Aesthetic Improvement Scale (IGAS) and the Patient Global Assessment (PGA) grading scale, ranging from −1 (worsened) to 4 (excellent improvement: 76–100%). Two blinded dermatologists independently assessed standardized photographs at each visit (baseline, 2 weeks, 1, 2, 3, and 6 months). Disagreements were resolved by averaging scores. Participants also self-evaluated their improvement at each follow-up. Pain during injection was recorded using a 10-point Visual Analog Scale (VAS), and adverse events were assessed throughout this study, including erythema, bruising, irritation, dyschromia, and muscle paralysis.

5.6. Statistical Analysis

Data were analyzed using SPSS version 18.0 (IBM Corp., Armonk, NY, USA). Descriptive statistics were reported as mean values ± standard deviations (SD) for continuous variables and as frequencies and percentages for categorical variables. The Shapiro–Wilk test was used to assess normality.
For within-group comparisons over time, repeated-measures ANOVA was applied for normally distributed data, and the Friedman test was used for non-parametric data. For between-group comparisons, paired t-tests or Wilcoxon signed-rank tests were performed, depending on data distribution. A p-value < 0.05 was considered statistically significant.

6. Study Limitations

This study was limited by its relatively small sample size and its focus on Thai patients with Fitzpatrick skin types IV–V, potentially limiting its generalizability to other populations. Future studies should include more diverse cohorts and longer follow-ups. Incorporating advanced objective imaging tools and exploring combination or comparative therapies could further refine our understanding of BoNT-A’s role in melasma treatment.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/toxins17070349/s1: Figure S1. Pore volume and area assessed with Antera®. Figure S2. Investigator Global Aesthetic Improvement Scale (IGAS) of melasma improvement in (a) 1:5 dilution and (b) 1:10 dilution. Figure S3. CONSORT 2025 flow diagram. Table S1. Assessment of Sebumeter®. Table S2. Assessment of mean pore volume and mean pore area with Antera®. Video S1. A treatment procedure.

Author Contributions

Methodology, T.T., J.P. and R.M.R.A.-C.; software, W.B. and S.S.; formal analysis, T.T., J.P. and R.M.R.A.-C.; investigation, T.T., J.P., R.M.R.A.-C., P.M., P.T. and Y.N.; writing—original draft preparation, T.T., J.P. and R.M.R.A.-C.; writing—review and editing, T.T., J.P. and R.M.R.A.-C.; supervision, T.T., W.M. and R.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Hugel Inc., 61-20 Sinbuk-ro, Sinbuk-eup, Chuncheon-si, Gangwon-do, 24203, Republic of Korea; grant number: IIT-HG-Tx-20250610-01.

Institutional Review Board Statement

This study was conducted according to the guidelines of the Declaration of Helsinki and was approved by the Ethics Committee of the Siriraj Institutional Review Board (si 457/2023; initial approval in 9 June 2023, renewed on 9 June 2024).

Informed Consent Statement

Written informed consent was obtained for the publication and use of all patients’ images before their enrollment in this study.

Data Availability Statement

The original contributions presented in this study are included in this article and Supplementary Materials. Further inquiries can be directed to the corresponding author.

Conflicts of Interest

The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Chang, M.W. Disorders of hyperpigmentation. Dermatology 2008, 2, 939–964. [Google Scholar]
  2. Artzi, O.; Horovitz, T.; Bar-Ilan, E.; Shehadeh, W.; Koren, A.; Zusmanovitch, L.; Mehrabi, J.N.; Salameh, F.; Isman Nelkenbaum, G.; Zur, E. The pathogenesis of melasma and implications for treatment. J. Cosmet. Dermatol. 2021, 20, 3432–3445. [Google Scholar] [CrossRef]
  3. Zhu, J.-W.; Ni, Y.-J.; Tong, X.-Y.; Guo, X.; Wu, X.-P. Activation of VEGF receptors in response to UVB promotes cell proliferation and melanogenesis of normal human melanocytes. Exp. Cell Res. 2020, 387, 111798. [Google Scholar] [CrossRef] [PubMed]
  4. Kim, E.H.; Kim, Y.C.; Lee, E.-S.; Kang, H.Y. The vascular characteristics of melasma. J. Dermatol. Sci. 2007, 46, 111–116. [Google Scholar] [CrossRef]
  5. Gilchrest, B.A.; Park, H.-Y.; Eller, M.S.; Yaar, M. Mechanisms of ultraviolet light-induced pigmentation. Photochem. Photobiol. 1996, 63, 1–10. [Google Scholar] [CrossRef] [PubMed]
  6. González-Molina, V.; Martí-Pineda, A.; González, N. Topical treatments for melasma and their mechanism of action. J. Clin. Aesthetic Dermatol. 2022, 15, 19. [Google Scholar]
  7. Flynn, T.C. Botulinum toxin: Examining duration of effect in facial aesthetic applications. Am. J. Clin. Dermatol. 2010, 11, 183–199. [Google Scholar] [CrossRef]
  8. Torres, S.; Hamilton, M.; Sanches, E.; Starovatova, P.; Gubanova, E.; Reshetnikova, T. Neutralizing antibodies to botulinum neurotoxin type A in aesthetic medicine: Five case reports. Clin. Cosmet. Investig. Dermatol. 2013, 7, 11–17. [Google Scholar] [CrossRef]
  9. Sharma, R.; Zhao, H.; Al-Saleem, F.H.; Ubaid, A.S.; Puligedda, R.D.; Segan, A.T.; Lindorfer, M.A.; Bermudez, R.; Elias, M.; Adekar, S.P. Mechanisms of enhanced neutralization of botulinum neurotoxin by monoclonal antibodies conjugated to antibodies specific for the erythrocyte complement receptor. Mol. Immunol. 2014, 57, 247–254. [Google Scholar] [CrossRef]
  10. Carruthers, A.; de Almeida, C.J. Botulinum Toxin. Dermatology 2018, 4, 2661–2672. [Google Scholar] [CrossRef]
  11. Schlessinger, J.; Gilbert, E.; Cohen, J.L.; Kaufman, J. New uses of abobotulinumtoxinA in aesthetics. Aesthetic Surg. J. 2017, 37, S45–S58. [Google Scholar] [CrossRef]
  12. Peng Chen, Z.; Morris, J.G., Jr.; Rodriguez, R.L.; Wagle Shukla, A.; Tapia-Nunez, J.; Okun, M.S. Emerging opportunities for serotypes of botulinum neurotoxins. Toxins 2012, 4, 1196–1222. [Google Scholar] [CrossRef] [PubMed]
  13. Friedland, S.; Burde, R.M. Porcelinizing discolorization of the periocular skin following botulinum A toxin injections. J. Neuro-Ophthalmol. Off. J. N. Am. Neuro-Ophthalmol. Soc. 1996, 16, 70–72. [Google Scholar]
  14. Jung, J.-A.; Kim, B.-J.; Kim, M.-S.; You, H.-J.; Yoon, E.-S.; Dhong, E.-S.; Park, S.-H.; Kim, D.-W. Protective effect of botulinum toxin against ultraviolet-induced skin pigmentation. Plast. Reconstr. Surg. 2019, 144, 347–356. [Google Scholar] [CrossRef] [PubMed]
  15. Erdil, D.; Manav, V.; Türk, C.B.; Kara Polat, A.; Koku Aksu, A.E. The clinical effect of botulinum toxin on pigmentation. Int. J. Dermatol. 2023, 62, 250–256. [Google Scholar] [CrossRef]
  16. Vachiramon, V.; Kositkuljorn, C.; Leerunyakul, K.; Rattananukrom, T.; Jurairattanaporn, N. A Study of Botulinum Toxin A for Ultraviolet-Induced Hyperpigmentation: A Randomized Controlled Trial. Dermatol. Surg. 2021, 47, e174–e178. [Google Scholar] [CrossRef] [PubMed]
  17. Vachiramon, V.; Anuntrangsee, T.; Palakornkitti, P.; Jurairattanaporn, N.; Harnchoowong, S. Incobotulinum Toxin Type A for Treatment of Ultraviolet-B-Induced Hyperpigmentation: A Prospective, Randomized, Controlled Trial. Toxins 2022, 14, 417. [Google Scholar] [CrossRef]
  18. Jurairattanaporn, N.; Palakornkitti, P.; Anuntrangsee, T.; Vachiramon, V. Study of botulinum toxin type A for the treatment of ultraviolet B--induced hyperpigmentation: A prospective, randomized, controlled trial. J. Cosmet. Dermatol. 2022, 21, 3343–3350. [Google Scholar] [CrossRef]
  19. Carruthers, J.; Carruthers, A. The effect of full-face broadband light treatments alone and in combination with bilateral crow’s feet botulinum toxin type A chemodenervation. Dermatol. Surg. 2004, 30, 355–366. [Google Scholar] [CrossRef]
  20. Yamauchi, P.; Lask, G.; Lowe, N. Botulinum toxin type A gives adjunctive benefit to periorbital laser resurfacing. J. Cosmet. Laser Ther. 2004, 6, 145–148. [Google Scholar] [CrossRef]
  21. Gugerell, A.; Kober, J.; Schmid, M.; Buchberger, E.; Kamolz, L.-P.; Keck, M. Botulinum toxin A: Dose-dependent effect on reepithelialization and angiogenesis. Plast. Reconstr. Surg.-Glob. Open 2016, 4, e837. [Google Scholar] [CrossRef]
  22. Dayan, S.H.; Pritzker, R.N.; Arkins, J.P. A new treatment regimen for rosacea: OnabotulinumtoxinA. J. Drugs Dermatol. 2012, 11, e76–e79. [Google Scholar] [PubMed]
  23. Bloom, B.S.; Payongayong, L.; Mourin, A.; Goldberg, D.J. Impact of intradermal abobotulinumtoxinA on facial erythema of rosacea. Dermatol. Surg. 2015, 41, S9–S16. [Google Scholar] [CrossRef] [PubMed]
  24. Park, K.Y.; Hyun, M.Y.; Jeong, S.Y.; Kim, B.J.; Kim, M.N.; Hong, C.K. Botulinum toxin for the treatment of refractory erythema and flushing of rosacea. Dermatology 2015, 230, 299–301. [Google Scholar] [CrossRef]
  25. Dayan, S.H.; Ashourian, N.; Cho, K. A Pilot, Double-Blind, Placebo-Controlled Study to Assess the Efficacy and Safety of IncobotulinumtoxinA Injections in the Treatment of Rosacea. J. Drugs Dermatol. JDD 2017, 16, 549–554. [Google Scholar] [PubMed]
  26. Park, K.Y.; Kwon, H.J.; Kim, J.M.; Jeong, G.J.; Kim, B.J.; Seo, S.J.; Kim, M.N. A pilot study to evaluate the efficacy and safety of treatment with botulinum toxin in patients with recalcitrant and persistent erythematotelangiectatic rosacea. Ann. Dermatol. 2018, 30, 688–693. [Google Scholar] [CrossRef]
  27. Kim, M.J.; Kim, J.H.; Cheon, H.I.; Hur, M.S.; Han, S.H.; Lee, Y.W.; Choe, Y.B.; Ahn, K.J. Assessment of skin physiology change and safety after intradermal injections with botulinum toxin: A randomized, double-blind, placebo-controlled, split-face pilot study in rosacea patients with facial erythema. Dermatol. Surg. 2019, 45, 1155–1162. [Google Scholar] [CrossRef]
  28. Al-Niaimi, F.; Glagoleva, E.; Araviiskaia, E. Pulsed dye laser followed by intradermal botulinum toxin type-A in the treatment of rosacea-associated erythema and flushing. Dermatol. Ther. 2020, 33, e13976. [Google Scholar] [CrossRef]
  29. Zhang, H.; Tang, K.; Wang, Y.; Fang, R.; Sun, Q. Use of botulinum toxin in treating rosacea: A systematic review. Clin. Cosmet. Investig. Dermatol. 2021, 14, 407–417. [Google Scholar] [CrossRef]
  30. Calvisi, L.; Diaspro, A.; Sito, G. Microbotox: A prospective evaluation of dermatological improvement in patients with mild--to--moderate acne and erythematotelangiectatic rosacea. J. Cosmet. Dermatol. 2022, 21, 3747–3753. [Google Scholar] [CrossRef]
  31. Tong, Y.; Luo, W.; Gao, Y.; Liu, L.; Tang, Q.; Wa, Q. A randomized, controlled, split—Face study of botulinum toxin and broadband light for the treatment of erythematotelangiectatic rosacea. Dermatol. Ther. 2022, 35, e15395. [Google Scholar] [CrossRef] [PubMed]
  32. Yang, R.; Liu, C.; Liu, W.; Luo, J.; Cheng, S.; Mu, X. Botulinum toxin A alleviates persistent erythema and flushing in patients with erythema telangiectasia rosacea. Dermatol. Ther. 2022, 12, 2285–2294. [Google Scholar] [CrossRef] [PubMed]
  33. Suksantilap, S.; Chalermchai, T.; Paichitrojjana, A. The Efficacy of Intradermal Injection of Botulinum Toxin A In The Treatment of Dermal and Mixed Type, Melasma. In Proceedings of the 4th National Academic Conference and Research Presentation Graduate School Conference 2022 iHappiness: Sustainable Happiness and Good Quality of Life in the Digital Age (Suan Sunandha Rajabhat University, 2022), Bangkok, Thailand, 27 May 2022. [Google Scholar]
  34. Thanasarnaksorn, W.; Supasiri, T.; Panich, U.; Thanachaiphiwat, S.; Salakshna, N. Intradermal Botulinum Toxin A for Melasma: A Randomized Split—Face Study Trial and In Vitro Study of Its Antimelanogenic Effect. Dermatol. Ther. 2025, 2025, 5550483. [Google Scholar] [CrossRef]
  35. Kania, B.; Lolis, M.; Goldberg, D. Melasma Management: A Comprehensive Review of Treatment Strategies Including BTX—A. J. Cosmet. Dermatol. 2025, 24, e16669. [Google Scholar] [CrossRef]
  36. Carmichael, N.M.E.; Dostrovsky, J.O.; Charlton, M.P. Peptide-mediated transdermal delivery of botulinum neurotoxin type A reduces neurogenic inflammation in the skin. Pain 2010, 149, 316–324. [Google Scholar] [CrossRef]
  37. Pomerantz, H.; Christman, M.P.; Bloom, B.S.; Lederhandler, M.; Feng, H.; Holmes, J.; Geronemus, R.G. Dynamic optical coherence tomography of cutaneous blood vessels in melasma and vessel response to oral tranexamic acid. Lasers Surg. Med. 2021, 53, 861–864. [Google Scholar] [CrossRef]
  38. Kim, Y.J.; Kim, J.-H.; Lee, K.-J.; Choi, M.-M.; Kim, Y.H.; Rhie, G.-e.; Yoo, C.-K.; Cha, K.; Shin, N.-R. Botulinum neurotoxin type A induces TLR2-mediated inflammatory responses in macrophages. PLoS ONE 2015, 10, e0120840. [Google Scholar] [CrossRef]
  39. Kellogg, D.L., Jr. In vivo mechanisms of cutaneous vasodilation and vasoconstriction in humans during thermoregulatory challenges. J. Appl. Physiol. 2006, 100, 1709–1718. [Google Scholar] [CrossRef]
  40. Kellogg, D.L., Jr.; Pérgola, P.E.; Piest, K.L.; Kosiba, W.A.; Crandall, C.G.; Grossmann, M.; Johnson, J.M. Cutaneous active vasodilation in humans is mediated by cholinergic nerve cotransmission. Circ. Res. 1995, 77, 1222–1228. [Google Scholar] [CrossRef]
  41. Zhou, J.; Feng, J.-Y.; Wang, Q.; Shang, J. Calcitonin gene-related peptide cooperates with substance P to inhibit melanogenesis and induces apoptosis of B16F10 cells. Cytokine 2015, 74, 137–144. [Google Scholar] [CrossRef]
  42. Filipović, B.; Matak, I.; Bach-Rojecky, L.; Lacković, Z. Central action of peripherally applied botulinum toxin type A on pain and dural protein extravasation in rat model of trigeminal neuropathy. PLoS ONE 2012, 7, e29803. [Google Scholar] [CrossRef] [PubMed]
  43. Picelli, A.; Tamburin, S.; Di Censo, R.; Smania, N.; Filippetti, M. Does the Diffusion Profile Differ Between Botulinum Toxin Type a Formulations? Implications for the Management of Post-Stroke Spasticity. Toxins 2024, 16, 480. [Google Scholar] [CrossRef] [PubMed]
  44. Brodsky, M.A.; Swope, D.M.; Grimes, D. Diffusion of botulinum toxins. Tremor Other Hyperkinetic Mov. 2012, 2, tre-02-85-417-1. [Google Scholar] [CrossRef]
  45. Klein, A.W.; Carruthers, A.; Fagien, S.; Lowe, N.J. Comparisons among botulinum toxins: An evidence-based review. Plast. Reconstr. Surg. 2008, 121, 413e–422e. [Google Scholar] [CrossRef]
  46. Hopewell, S.; Chan, A.-W.; Collins, G.S.; Hróbjartsson, A.; Moher, D.; Schulz, K.F.; Tunn, R.; Aggarwal, R.; Berkwits, M.; Berlin, J.A. CONSORT 2025 statement: Updated guideline for reporting randomised trials. Lancet 2025, 405, 1633–1640. [Google Scholar] [CrossRef] [PubMed]
  47. Al-Fouzan, A.F.; Mokeem, L.S.; Al-Saqat, R.T.; Alfalah, M.A.; Alharbi, M.A.; Al-Samary, A.E. Botulinum Toxin for the Treatment of Gummv Smile. J. Contemp. Dent. Pract. 2017, 18, 474–478. [Google Scholar] [CrossRef]
  48. Gong, X.; Tang, H.-N.; Zhang, A.-R.; Wang, Z.; Tang, Z.-H.; Han, X.-F.; Su, J.-Z. Application of botulinum toxin at the Yonsei point for the treatment of gummy smile: A randomized controlled trial. Plast. Reconstr. Surg. 2024, 153, 711e–721e. [Google Scholar] [CrossRef]
  49. Hur, M.S.; Youn, K.H.; Kim, H.J. New insight regarding the zygomaticus minor as related to cosmetic facial injections. Clin. Anat. 2018, 31, 974–980. [Google Scholar] [CrossRef]
  50. Mazzuco, R.; Hexsel, D. Gummy smile and botulinum toxin: A new approach based on the gingival exposure area. J. Am. Acad. Dermatol. 2010, 63, 1042–1051. [Google Scholar] [CrossRef]
  51. Mekawy, K.M.; Sadek, A.; Seddeik Abdel-Hameed, A.K. Micro-needling versus fractional carbon dioxide laser for delivery of tranexamic acid in the treatment of melasma: A split-face study. J. Cosmet. Dermatol. 2021, 20, 460–465. [Google Scholar] [CrossRef]
Figure 1. (a) Mean Hemi-mMASI score dilution 1:5; (b) mean Hemi-mMASI score dilution 1:10. p < 0.05 (*), p < 0.01 (**); ns = not significant. Statistical comparison versus baseline.
Figure 1. (a) Mean Hemi-mMASI score dilution 1:5; (b) mean Hemi-mMASI score dilution 1:10. p < 0.05 (*), p < 0.01 (**); ns = not significant. Statistical comparison versus baseline.
Toxins 17 00349 g001
Figure 2. Clinical outcomes after treatment at different dilutions.
Figure 2. Clinical outcomes after treatment at different dilutions.
Toxins 17 00349 g002
Figure 3. The mean brown spot scores for the 1:5 (a) and 1:10 (b) dilutions, as well as the mean red area scores for the 1:5 (c) and 1:10 (d) dilutions, evaluated throughout the treatment period. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***), p < 0.0001 (****); ns = not significant. Statistical comparisons were performed versus baseline.
Figure 3. The mean brown spot scores for the 1:5 (a) and 1:10 (b) dilutions, as well as the mean red area scores for the 1:5 (c) and 1:10 (d) dilutions, evaluated throughout the treatment period. p < 0.05 (*), p < 0.01 (**), p < 0.001 (***), p < 0.0001 (****); ns = not significant. Statistical comparisons were performed versus baseline.
Toxins 17 00349 g003aToxins 17 00349 g003b
Figure 4. Mean change in Hemi-modified Melasma Area and Severity Index comparing between two dilutions in the (a) non-telangiectatic and (b) telangiectatic melasma groups.
Figure 4. Mean change in Hemi-modified Melasma Area and Severity Index comparing between two dilutions in the (a) non-telangiectatic and (b) telangiectatic melasma groups.
Toxins 17 00349 g004
Figure 5. Clinical outcomes of telangiectatic-type melasma assessed with VISIA® imaging (Canfield Scientific, Inc., Parsippany, NJ, USA) following treatment with dilutions 1:5 (a) and 1:10 (b).
Figure 5. Clinical outcomes of telangiectatic-type melasma assessed with VISIA® imaging (Canfield Scientific, Inc., Parsippany, NJ, USA) following treatment with dilutions 1:5 (a) and 1:10 (b).
Toxins 17 00349 g005
Figure 6. Patient Global Assessment (PGA) of melasma improvement in (a) 1:5 dilution and (b) 1:10 dilution.
Figure 6. Patient Global Assessment (PGA) of melasma improvement in (a) 1:5 dilution and (b) 1:10 dilution.
Toxins 17 00349 g006
Figure 7. Location and amount of Letibotulinum toxin A injections.
Figure 7. Location and amount of Letibotulinum toxin A injections.
Toxins 17 00349 g007
Table 1. Demographic data of subjects enrolled in this study.
Table 1. Demographic data of subjects enrolled in this study.
Characteristics Value (n = 30)
Age in years
Mean ± SD * (min–max) 47 ± 6.60 (32–62)
Sex, n (%)
  Male 1 (3%)
  Female 29 (96.67%)
Fitzpatrick Skin type, n (%)
  Type III 4 (13.33%)
  Type IV 21 (70%)
  Type V 5 (16.67%)
Melasma type, n (%)Non-telangiectatic16 (53.33%)
Telangiectatic14 (46.67%)
Baseline Hemi-mMASI score
1:5 dilution4.44 ± 1.82
1:10 dilution4.66 ± 1.85
Baseline Hemi-mMASI score
Non-telangiectatic1:5 dilution3.78 ± 1.45
1:10 dilution3.95 ± 0.90
Telangiectatic1:5 dilution5.20 ± 1.96
1:10 dilution5.48 ± 2.30
Mean pain score
Mean ± SD * (min–max)1:5 dilution5.13 ± 2.29 (min = 0, max = 9)
1:10 dilution5.23 ± 2.21(min = 0, max = 9)
* SD, standard deviation.
Table 2. Mean Hemi-modified Melasma Area and Severity Index.
Table 2. Mean Hemi-modified Melasma Area and Severity Index.
Follow-UpMean Hemi-mMASI
(1:5)
Mean Hemi-mMASI
(1:10)
p-Value
Comparing Two Concentrations
Baseline4.38 ± 1.664.47 ± 1.63
2-week
follow-up
4.16 ± 1.69 (p = 0.158)4.06 ± 1.48 (p = 0.006) **>0.99
1-month
follow-up
3.87 ± 1.46 (p = 0.049) *3.94 ± 1.22 (p = 0.082)>0.99
2-month
follow-up
3.95 ± 1.60 (p = 0.080)3.84 ± 1.45 (p = 0.013) *>0.99
4-month
follow-up
3.97 ± 1.59 (p = 0.100)3.70 ± 1.39 (p = 0.002) **0.847
6-month
follow-up
3.78 ± 1.49 (p = 0.043) *3.53 ± 1.32 (p = 0.002) **>0.99
p-value < 0.05 (*), p-value < 0.01 (**). Statistical comparison was made versus baseline.
Table 3. Assessment of VISIA® complexion analysis (Canfield Scientific, Inc., Parsippany, NJ, USA) percentage data.
Table 3. Assessment of VISIA® complexion analysis (Canfield Scientific, Inc., Parsippany, NJ, USA) percentage data.
Follow-UpBrown Spots
(1:5)
Brown Spots
(1:10)
Red Areas
(1:5)
Red Areas
(1:10)
Baseline17.93 ± 5.7917.95 ± 5.6113.68 ± 11.7714.69 ± 11.43
2-week follow-up16.88 ± 5.2317.02 ± 5.1914.15 ± 11.3115.10 ± 11.25
(0.131)(0.203)(>0.99)(>0.99)
1-month follow-up16.30 ± 4.9916.41 ± 5.2712.61 ± 11.3214.09 ± 11.16
(0.017) *(0.007) **(>0.99)(>0.99)
2-month follow-up16.24 ± 4.2816.38 ± 4.8712.40 ± 10.6613.05 ± 10.35
(0.001) **(0.001) **(>0.99)(0.834)
4-month follow-up16.11 ± 4.6115.94 ± 4.6911.68 ± 10.6512.78 ± 10.14
(0.010) *(0.001) ***(0.208)(0.348)
6-month follow-up15.64 ± 4.4815.5 ± 4.7111.76 ± 10.7512.32 ± 10.45
(0.002) **(<0.001) ****(0.227)(0.032) *
p < 0.05 (*), p < 0.01 (**), p < 0.001 (***), p < 0.0001 (****). Statistical comparisons were performed versus baseline.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Pongklaokam, J.; Manuskiatti, W.; Wanitphakdeedecha, R.; Maneeprasopchoke, P.; Thongjaroensirikul, P.; Nokdhes, Y.; Abad-Constantino, R.M.R.; Bhorntarakcharoen, W.; Sittiwanaruk, S.; Techapichetvanich, T. Efficacy and Safety of Letibotulinum Toxin A for the Treatment of Melasma in Two Different Dilutions: A Randomized Double-Blind Split-Face Study. Toxins 2025, 17, 349. https://doi.org/10.3390/toxins17070349

AMA Style

Pongklaokam J, Manuskiatti W, Wanitphakdeedecha R, Maneeprasopchoke P, Thongjaroensirikul P, Nokdhes Y, Abad-Constantino RMR, Bhorntarakcharoen W, Sittiwanaruk S, Techapichetvanich T. Efficacy and Safety of Letibotulinum Toxin A for the Treatment of Melasma in Two Different Dilutions: A Randomized Double-Blind Split-Face Study. Toxins. 2025; 17(7):349. https://doi.org/10.3390/toxins17070349

Chicago/Turabian Style

Pongklaokam, Juthapa, Woraphong Manuskiatti, Rungsima Wanitphakdeedecha, Pitchaya Maneeprasopchoke, Panwadee Thongjaroensirikul, Yanin Nokdhes, Rona Maria R. Abad-Constantino, Woramate Bhorntarakcharoen, Sariya Sittiwanaruk, and Thanya Techapichetvanich. 2025. "Efficacy and Safety of Letibotulinum Toxin A for the Treatment of Melasma in Two Different Dilutions: A Randomized Double-Blind Split-Face Study" Toxins 17, no. 7: 349. https://doi.org/10.3390/toxins17070349

APA Style

Pongklaokam, J., Manuskiatti, W., Wanitphakdeedecha, R., Maneeprasopchoke, P., Thongjaroensirikul, P., Nokdhes, Y., Abad-Constantino, R. M. R., Bhorntarakcharoen, W., Sittiwanaruk, S., & Techapichetvanich, T. (2025). Efficacy and Safety of Letibotulinum Toxin A for the Treatment of Melasma in Two Different Dilutions: A Randomized Double-Blind Split-Face Study. Toxins, 17(7), 349. https://doi.org/10.3390/toxins17070349

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop