Since abnormal keratinocyte (KC) proliferation and differentiation as well as defective E cadherin expression were reported in vitiligo lesions, the investigators set to study the potential efficacy of combining Retinoids, which are known to improve KC proliferation and differentiation and increase the expression of adhesion molecules, with narrowband UVB in the treatment of vitiligo.
• Twenty patients with generalized vitiligo will be included in this study. All patients will be subjected to: * Clinical evaluation: * An informed written consent. * History taking include age, previous treatment, disease activity * Clinical examination including Vitiligo Area Scoring Index (VASI) and Vitiligo Disease Activity Score (VIDA) * Photography (before starting the treatment and every 2 weeks till the end of the study) Laboratory evaluation: * 2 mm punch skin biopsies will be taken from vitiligo patients, 1 from lesional and the other from perilesional skin before treatment. * The patients will be randomly assigned to two groups: Group A: patients will receive three NB-UVB sessions per week for 48 sessions. Group B: patients will receive three NB-UVB sessions per week for 48 sessions combined with acitretin in a dose of 0.3mg/kg/day daily. * Controls: 20 individuals age and sex matched will be biopsied from the skin of their abdominoplasty surgery. * Another two 2 mm punch skin biopsies will be taken from lesional and perilesional skin at the onset of repigmentation if repigmentation starts before completion of the 48 treatment session or after completion of the treatment period if repigmentation does not occur. * .All biopsies from patients and controls will be stained Immunohistochemically by anti-E cadherin antibody.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
20
The patients will receive the drug and the effect on repigmentation on vitiligo lesions will be observed
Patients receive nbUVB session 3 times per week
Cairo University
Cairo, Egypt
RECRUITINGDetermining whether addition of acitretin is beneficial for vitiligo patients or not using Vitiligo Area Scoring Index
The number of patients who will achieve 100%, 75% and 50% repigmentation of vitiligo lesions will be compared between group A (nbUVB) and group B (nbUVB+ acitretin) after 48 nbUVB sessions. The comparison of the 2 groups will be assessed using Vitiligo Area Scoring Index (VASI)
Time frame: 4-5 months
Determining whether addition of acitretin is beneficial for vitiligo patients or not using Vitiligo Disease Activity Score.
The number of patients who will achieve 100%, 75% and 50% repigmentation of vitiligo lesions will be compared between group A (nbUVB) and group B (nbUVB+ acitretin) after 48 nbUVB sessions. The comparison of the 2 groups will be assessed using Vitiligo Disease Activity Score (VIDA).
Time frame: 4-5 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.