AI Article Synopsis

  • Vitiligo does not show clear inflammatory symptoms like other skin disorders, making it challenging to assess and treat.
  • This study investigates serum levels of soluble CD27 (sCD27) and macrophage Migration Inhibitory Factor (MIF) as potential biomarkers for better disease management in vitiligo.
  • Results indicate higher serum levels of sCD27 and MIF in vitiligo patients compared to healthy controls, with significant correlations between these biomarkers and disease activity, especially sCD27.

Article Abstract

Contrary to other inflammatory skin disorders like psoriasis or atopic dermatitis, vitiligo does not present with distinct inflammatory symptoms that can be easily evaluated by clinical examination. Identification of a putative biomarker to inform early and accurate treatment responses could be of considerable value. This study aims to validate levels of serum soluble CD27 (sCD27) and macrophage Migration Inhibitory Factor (MIF) as biomarkers of vitiligo to improve the quality of disease management. This cross-sectional study was conducted on 32 vitiligo patients, stratified into two subgroups of 22 active and 10 stable vitiligo patients; the stable group containing 1 segmental and 9 nonsegmental presentations, and 32 matched healthy individuals as the control group. Of the 32 patients in the study, 21 were female and 11 were male with a median age of 30 years. The measurements of the study parameters of sCD27 and MIF in the serum were carried out through blood sampling and followed up for three months at onemonth intervals for stable vitiligo cases. Mean serum levels of sCD27 and MIF were significantly higher in vitiligo patients than in the control group. A positive correlation was observed in active vitiligo cases between both serum MIF and sCD27 levels and the spreading item of Vitiligo European Task Force (VETF) score as an indicator of disease activity. Serum sCD27 and MIF levels in vitiligo patients were observed to be higher than that of controls with greater correlation found for sCD27 with disease activity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073715PMC
http://dx.doi.org/10.4081/dr.2019.8265DOI Listing

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