» Articles » PMID: 37298700

Etiopathogenesis and Emerging Methods for Treatment of Vitiligo

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 Jun 10
PMID 37298700
Authors
Affiliations
Soon will be listed here.
Abstract

Vitiligo is an acquired chronic depigmenting disorder of skin. It is mostly asymptomatic and characterized by amelanotic macules and patches that affects 0.5% to 2% of the world's population. The etiology of vitiligo has not been clearly elucidated and multiple theories have been proposed regarding the causes of the disorder. Among the most prevalent theories, the genetic predisposition, oxidative stress theory, promotion of cellular stress and pathologic influence of lymphocytes T have been highlighted. As a result of increases in in-depth knowledge concerning the pathogenetic processes in vitiligo, we review the most recent information concerning its etiopathogenesis and treatment methods including topical and oral Janus kinase inhibitors, prostaglandins and their analogues, namely afamelanotide, Wnt/β-catenin-signaling agonists and cell-based therapies. Topical ruxolitinib has been registered for vitiligo treatment, whereas other agents as oral ritlecitinib, afamelanotide and latanoprost have been studied in ongoing clinical trials. New highly effective therapeutic strategies may be developed thanks to molecular and genetic studies.

Citing Articles

Short-term efficacy and safety of upadacitinib combined with 308 excimer light versus upadacitinib alone and 308 excimer light alone in patients with progressing facial vitiligo.

Zhang W, Zhai S, Dou J, Zhang S, Liu H Arch Dermatol Res. 2025; 317(1):252.

PMID: 39821379 DOI: 10.1007/s00403-024-03717-3.


Bioinformatic analysis of ferroptosis related biomarkers and potential therapeutic targets in vitiligo.

Liu L, Deng L, Guan L, Hu Y, Li Q, Yu C Sci Rep. 2025; 15(1):2035.

PMID: 39814853 PMC: 11735852. DOI: 10.1038/s41598-025-86061-4.


Vitiligo: Clinical and Laboratory Characteristics in 573 Saudi Patients.

AlJasser M Clin Cosmet Investig Dermatol. 2024; 17:2887-2899.

PMID: 39712943 PMC: 11660655. DOI: 10.2147/CCID.S499794.


Role of Cytokines and Chemokines in Vitiligo and Their Therapeutic Implications.

Kadziela M, Kutwin M, Karp P, Wozniacka A J Clin Med. 2024; 13(16).

PMID: 39201060 PMC: 11355229. DOI: 10.3390/jcm13164919.


Afamelanotide in protoporphyria and other skin diseases: a review.

Polanska A, Wegner J, Nutbohm P, Staubach P, Zaba R, Danczak-Pazdrowska A Postepy Dermatol Alergol. 2024; 41(2):149-154.

PMID: 38784937 PMC: 11110213. DOI: 10.5114/ada.2024.138818.


References
1.
Vanderweil S, Amano S, Ko W, Richmond J, Kelley M, Senna M . A double-blind, placebo-controlled, phase-II clinical trial to evaluate oral simvastatin as a treatment for vitiligo. J Am Acad Dermatol. 2016; 76(1):150-151.e3. PMC: 5176345. DOI: 10.1016/j.jaad.2016.06.015. View

2.
Fraczek A, Owczarczyk-Saczonek A, Placek W . The Role of T Cells in the Pathogenesis of Vitiligo-A Review of the Current State-Of-The-Art. Int J Mol Sci. 2020; 21(10). PMC: 7278984. DOI: 10.3390/ijms21103552. View

3.
Thier R, Bruning T, Roos P, Rihs H, Golka K, Ko Y . Markers of genetic susceptibility in human environmental hygiene and toxicology: the role of selected CYP, NAT and GST genes. Int J Hyg Environ Health. 2003; 206(3):149-71. DOI: 10.1078/1438-4639-00209. View

4.
Anbar T, El-Ammawi T, Abdel-Rahman A, Hanna M . The effect of latanoprost on vitiligo: a preliminary comparative study. Int J Dermatol. 2014; 54(5):587-93. DOI: 10.1111/ijd.12631. View

5.
Jin Y, Birlea S, Fain P, Ferrara T, Ben S, Riccardi S . Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. Nat Genet. 2012; 44(6):676-80. PMC: 3366044. DOI: 10.1038/ng.2272. View