Pui-Ying Leong
Tsu-Man Chiu1,2,4†
James Cheng-Chung Wei
An-Ping Huo- 1Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan
- 2School of Medicine, Chung Shan Medical University, Taichung, Taiwan
- 3Division of Allergy, Immunology and Rheumatology, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan
- 4Department of Dermatology, Chung Shan Medical University Hospital, Taichung, Taiwan
The co-occurrence of psoriasis (PsO) and vitiligo is rare in Asian countries, especially in children. This case report presents the first-ever occurrence of PsO combined with vitiligo in an Asian boy under 6 years of age, in whom symptom improvement was observed after the use of methotrexate (MTX) as the sole treatment. Although previous studies have indicated that there is a close correlation between the two diseases, methotrexate (MTX), which is a commonly used treatment for PsO, is not a standard treatment for vitiligo. Even with advanced progress in biologics and Janus kinase inhibitor (JAKi), the biologics and JAKi used in vitiligo are still inconsistent. In our case report, the successful use of MTX indicated that there are shared immune pathways between PsO and vitiligo. Further exploration is needed to optimize the treatment options for this co-occurrence of PsO and vitiligo.
Introduction
Psoriasis (PsO) is more prevalent in Northern European nations than in East Asia (1), and vitiligo is less common among Asian Americans than individuals of other races (2). Consequently, the co-occurrence of PsO and vitiligo is frequent in Europe and the Americas but rare in Asia, especially among children under 10 years of age. We present the first-ever case of an Asian boy under 6 years of age who developed PsO combined with vitiligo. This child’s symptoms improved after only methotrexate (MTX) was administered. Based on this treatment experience and relevant literature, we discuss the correlation between PsO and vitiligo and the therapeutic role of MTX in treating these two conditions.
At 5 years of age, a young boy with no family history of PsO or vitiligo presented with psoriatic lesions on his elbows, knees, hands, and feet, along with associated nail changes. Initially, he was managed with topical corticosteroids at local clinics for his condition. One year later, at 6 years of age, vitiligo appeared to be generalized and included lesions of PsO that extended to the patient’s face and neck. At 7 years of age, he was brought to our outpatient department due to progressed vitiligo and PsO despite the addition of narrow-band ultraviolet B (NB-UVB) phototherapy for 3 months. A physical examination revealed vitiligo lesions all over the patient’s face, neck, hands, trunk, four limbs, palms, and soles, with typical psoriasis plaques on the patient’s knees, elbows, hands, and feet. In regard to psoriatic nails, crumble of more than half the nail bed area was observed on all 10 toenails, and the fingernails were also affected, with mild pitting and minimal onycholysis observed, but no subungual hyperkeratosis or crumble. No musculoskeletal symptoms or signs and no arthritis were observed at that time. All the hematologic, biochemical, and autoimmune examination results were within the normal range. He did not have the budget for treatment with biologics. Hence, our treatment target was focused only on his PsO and psoriatic nails, with low-dosage MTX (5 mg per week owing to his body surface area). During the initial 6-month period, monthly follow-up assessments were conducted to track treatment outcomes and potential side effects. Encouragingly, no adverse effects were observed, and the patient maintained normal levels of blood cells and normal liver function. PsO lesions improved approximately 4 weeks after treatment, and the vitiligo lesion improved approximately 8 weeks after treatment. These positive results underscore the favorable tolerability and effectiveness of the treatment regimen, and the follow-up interval was extended to every 2 months (for 6 months) and finally to every 3 months (to date). After 3 years of treatment at the same dosage of MTX, the psoriatic skin and nail lesions have improved slowly, the psoriasis area severity index (PASI) score has declined from 6.1 to 1.9, and the vitiligo has improved dramatically over time, with the vitiligo area scoring index (VASI) decreasing from 54.8 to 21.5, and with no signs or symptoms of arthritis observed during this period. The psoriatic nail lesions also improved slowly (approximately 18 months after treatment), and improved only partially after 3 years of treatment, with the right big toenail regrowing almost fully, approximately 50% of the nail bed area on the left big toenail regrowing, and the crumbling areas on the other toenails decreasing by approximately 30%, with only minimal residual pitting observed over all fingernails (Figures 1, 2).
Figure 1 Panels (A–D): Generalized co-occurrence of vitiligo and psoriasis before treatment.
Figure 2 Panels (E–H): Vitiligo responded better than psoriatic lesions to low-dose methotrexate treatment after 3 years.
Discussion
PsO is a chronic inflammatory skin disease characterized by well-demarcated erythematous plaques covered by excessive keratinocyte exfoliation. According to the Global Burden of Disease (GBD) Study 2019, its prevalence rate is 57.8 per 100,000 people and it is more common in Northern European nations (1). Vitiligo is an autoimmune disorder that causes the patchy loss of skin pigmentation by attacking melanocytes. It is less prevalent among Asian Americans than among individuals of other races (2). The co-occurrence of PsO and vitiligo was first reported by Selenyi in 1955 (3). PsO has a strong tendency to co-occur with other autoimmune/immune-mediated diseases, and research indicates that PsO patients may have a 25% chance of developing vitiligo during their lifetime (4). Similarly, PsO is the second most common comorbidity in vitiligo patients (5). Therefore, the co-occurrence of PsO and vitiligo is more frequent in individuals in Western countries than in Asian children. Until now, only six cases in which PsO co-occurred with vitiligo have been reported in Asian patients. These comprised four Korean patients, one Japanese patient, and one Chinese patient; the two Korean patients were adults and had previously been reported on in a study written in Korean (6, 7); of the other four patients, who were reported on in a study written in English, two were Korean adults (8, 9). In the Japanese patient, initial symptoms of vitiligo presented in childhood, and PsO co-occurred when she was 66 years old (10). The co-occurrence of PsO and vitiligo under the age of 18 years was observed in only the Chinese patients. The Chinese patient showed initial symptoms of vitiligo at 10 years of age, with PsO co-occurring 2 months later (11). Our patient is the youngest Asian child in whom the initial symptoms of co-occurrence of PsO and vitiligo presented below the age of 6 years.
Current studies have revealed that the interleukin (IL)-23/IL-17 pathogenic axis drives PsO. The activation of plasmacytoid dendritic cells promotes myeloid dendritic cell maturation and the production of tumor necrosis factor-α (TNF-α), IL-12, and IL-23, which leads to the activation of Th (T helper) 1 and Th17, and the subsequent secretion of inflammatory cytokines, such as TNF-α, IL-17, IL-21, and IL-22. These cytokines (especially IL-17) then activate keratinocytes and produce antimicrobial peptides, cytokines, and chemokines, contributing to inflammation amplification (12). Therefore, in addition to conventional synthetic diseases modified antirheumatic drugs (csDMARD), biologics are commonly used in treating PsO, including TNF inhibitor (TNFi), anti-IL-17 antibodies, anti-IL-17 receptor antibodies, anti-IL12/23 antibodies, anti-IL-23 antibodies, and Janus kinase inhibitor (JAKi).
Before 2013, no positive results associated with treating vitiligo using MTX had been published (13); only after 2015 did a few studies with a small number of patients reveal the effect of MTX in vitiligo (14, 15), and since 2020 a few positive results associated with MTX combined with low-dose steroids or phototherapy in vitiligo have also been reported in a small number of cases (16, 17). Yen et al. previously reported that PsO and vitiligo have similar pathogenic backgrounds. They are both cell-mediated Th1 diseases in which elevated TNF-α and interferon (INF) levels and the activation of the Th17 pathway are observed (18). After that, TNFi, anti-IL-17 antibodies, anti-IL-23 antibodies, and JAKi are reasonable in treating the co-occurrence of PsO and vitiligo. In recent vitiligo studies, the IFN-γ- CXCL9/10-CXCR3 axis appears important in vitiligo via inhibiting melanogenesis, inducing apoptosis of melanocytes, and further recruiting T cells to the skin. These are all involved in the JAK/signal transducer and activator of the transcription (STAT) pathway. In addition, cytokines, including heat shock protein 70i (HSP70i), IL-15, IL-17/23, and TNF, and also the wnt signaling pathway, regulatory T cells (Tregs), and micro-RNA (miRNAs), have also been proven to be involved in the pathogenesis of vitiligo. Based on the pathophysiology of vitiligo, the current treatment for moderate to severe vitiligo includes TNFi, anti-IL-17 antibody, anti-IL-23 antibody, and JAKi (19). However, many case reports have revealed that the use of these biologics in treating PsO or the co-occurrence of PsO and vitiligo, except for JAKi combined with phototherapy (20, 21), might induce the new onset of or worsen pre-existing vitiligo (22, 23). The first case of vitiligo successfully treated with JAKi was reported in 2015 (24). Later, positive results of topical JAKi in vitiligo were published in 2017 (25). Nevertheless, it was not until July 2022 that the Food and Drug Administration (FDA) approved topical ruxolitinib as a treatment for non-segmental vitiligo in patients above the age of 12 years. Although some oral JAKi studies in vitiligo had positive results, no oral JAKi are currently approved for treatment. In addition, the FDA-approved label for topical ruxolitinib features a pointed reminder that the relationship between the JAKs and their inhibition and vitiligo is not entirely understood. On the label it is stated that the “relevance of inhibition of specific JAK enzymes to therapeutic effectiveness is unknown.”
The efficacy of MTX in treating rheumatoid arthritis, psoriatic arthritis, and PsO was previously thought to be inherent to its action as a competitive inhibitor of dihydrofolate reductase (DHFR); enzymatic inhibition reduces the intracellular levels of downstream folate pathway intermediates required for nucleotide synthesis, and this results in impaired DNA replication. A possible new mechanism of MTX in immune disease, namely its inhibition of the JAK/STAT pathway, was proposed in 2015 (26). MTX has multiple mechanisms that potentially contribute to anti-inflammatory actions, including (a) inhibition of purine and pyrimidine synthesis, (b) transmethylation reactions, (c) the translocation of nuclear factor-κB (NF-κB) to the nucleus, (d) signaling via the JAK/STAT pathway, (e) nitric oxide production, and (f) the promotion of adenosine release and expression of specific long non-coding RNAs. Among these possible mechanisms, (c), (d), and (e) have been proposed to be the principal anti-inflammatory mechanisms (27). The (f) mechanism of anti-inflammation was previously included in the main mechanism, but a recent study revealed that the polymorphism of the genes involved in adenosine production and signaling could influence the response to MTX (28). The patient reported on in our case report started taking MTX in 2018; at that time, MTX was the first choice of first-line csDMARDs for moderate to severe PsO and was not considered helpful for vitiligo treatment, and JAKi, in both topical and oral form, had still not been approved for the treatment of vitiligo, especially in children under the age of 12 years. Therefore, in addition to presenting the youngest patient with co-occurrence of vitiligo and PsO, in our case report we present the successful treatment with MTX, especially of vitiligo and not just of PsO, as a piece of minor evidence that the JAK/STAT pathway may play an important role in both vitiligo and PsO.
Another interesting observation is that in our patient the PsO lesions were all found within the later onset vitiligo lesion area. From Sharquie’s report, 15 patients were found to have co-occurrence of PsO and vitiligo. The PsO lesions of eight patients were in the vitiligo lesions, and in another nine their PsO lesions were separate from the vitiligo lesions (29). Whether or not the excellent response of PsO and vitiligo to MTX in our patient is related to the fact that these two skin lesions (for two conditions with a common pathologic pathway) were in the same area still needs further study.
Conclusion
Li et al. summarized three possible mechanisms of the co-occurrence of vitiligo and PsO: (a) isomorphic reaction, (b) shared genetic basis of autoimmunity and inflammation, and (c) shared cellular immune pathways and related cellular molecules (11). Based on the occurrence of vitiligo following the onset of PsO, the lack of a traceable family history of PsO or vitiligo, and the good results with MTX treatment in both PsO and vitiligo in our case, we suggest that the co-occurrence of PsO and vitiligo is not a coincidence and may be related to the shared cellular immune pathways of both diseases. Although the effects of TNFi and anti-IL-17 antibodies on vitiligo are variable, the utilization of MTX in conjunction with steroids or phototherapy and the consideration of JAKi targeting the JAK/STAT pathway hold potential for treating vitiligo. However, it is important to note that the hypothesis regarding the involvement of the JAK/STAT pathway in vitiligo treatment needs to be substantiated with further evidence.
Data availability statement
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.
Ethics statement
Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author contributions
A-PH: Resources, Supervision, Writing – review & editing, Validation. P-YL: Writing – original draft, Investigation. T-MC: Writing – original draft, Investigation. JW: Supervision, Validation, Writing – review & editing.
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.
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Keywords: psoriasis, vitiligo, methotrexate, JAK, biologics
Citation: Leong P-Y, Chiu T-M, Wei JC-C and Huo A-P (2023) Case Report: Successful treatment with methotrexate in a 10-year-old boy with co-occurrence of generalized psoriasis and vitiligo. Front. Immunol. 14:1255909. doi: 10.3389/fimmu.2023.1255909
Received: 10 July 2023; Accepted: 13 September 2023;
Published: 03 October 2023.
Edited by:
Magda Carneiro-Sampaio, University of São Paulo, BrazilReviewed by:
William D. Shipman, Yale University, United StatesEmanuele Bizzi, ASST Fatebenefratelli Sacco, Italy
Copyright © 2023 Leong, Chiu, Wei and Huo. 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: An-Ping Huo, antonio.aphuo@msa.hinet.net; antoniohuo@gmail.com
†ORCID: An-Ping Huo, orcid.org/0000-0002-8285-1700
†These authors have contributed equally to this work and share first authorship