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A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo

BACKGROUND: There is evidence to support that vitiligo is linked to metabolic syndrome (MS), confirming its systemic nature. However, the underlying pathogenic mechanisms remain unknown. OBJECTIVES: To reveal the possible association of MS with vitiligo. We also attempted to study the connection bet...

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Autores principales: Mustafa, Amany I., Hamed, Ahmed M., Kadah, Ahmed S., Fawzy, Eman M., El Shimi, Ola S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373801/
https://www.ncbi.nlm.nih.gov/pubmed/37521222
http://dx.doi.org/10.4103/idoj.idoj_674_22
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author Mustafa, Amany I.
Hamed, Ahmed M.
Kadah, Ahmed S.
Fawzy, Eman M.
El Shimi, Ola S.
author_facet Mustafa, Amany I.
Hamed, Ahmed M.
Kadah, Ahmed S.
Fawzy, Eman M.
El Shimi, Ola S.
author_sort Mustafa, Amany I.
collection PubMed
description BACKGROUND: There is evidence to support that vitiligo is linked to metabolic syndrome (MS), confirming its systemic nature. However, the underlying pathogenic mechanisms remain unknown. OBJECTIVES: To reveal the possible association of MS with vitiligo. We also attempted to study the connection between some inflammatory markers and MS in vitiligo patients to evaluate their utility in predicting MS risk. MATERIALS AND METHODS: The study included 100 vitiligo patients with an age range between 18 to 60 years and 100 controls with matched age, gender, and body mass index. All subjects were tested for MS components. Serum visceral adipose tissue-derived serine protease inhibitor (vaspin), fatty acid binding protein 4 (FABP4), vascular adhesion protein 1 (VAP-1), chitinase-3-like protein 1 (YKL-40), and high-sensitivity C-reactive protein (hs-CRP) were also measured. RESULTS: Regarding MS, it was observed in 22.0% of vitiligo patients and 2.0% of control subjects (P < 0.001). Serum FABP4, VAP-1, YKL-40, and hs-CRP concentrations were higher in patients than in the control group (P < 0.05 each), and their levels showed high sensitivity and specificity to differentiate MS when using the receiver operating characteristic (ROC). Levels of these markers, except serum vaspin, were significantly positively correlated with lipid profile markers (except high-density lipoprotein cholesterol) and fasting blood glucose levels (P < 0.05 each). CONCLUSION: MS was more common in vitiligo patients. The levels of the biomarkers studied were significantly higher in vitiligo patients. Furthermore, their levels accurately predicted MS in vitiligo patients. According to current research, these markers may be useful in assessing MS risk in vitiligo patients. Extensive research, however, is required.
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spelling pubmed-103738012023-07-28 A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo Mustafa, Amany I. Hamed, Ahmed M. Kadah, Ahmed S. Fawzy, Eman M. El Shimi, Ola S. Indian Dermatol Online J Original Article BACKGROUND: There is evidence to support that vitiligo is linked to metabolic syndrome (MS), confirming its systemic nature. However, the underlying pathogenic mechanisms remain unknown. OBJECTIVES: To reveal the possible association of MS with vitiligo. We also attempted to study the connection between some inflammatory markers and MS in vitiligo patients to evaluate their utility in predicting MS risk. MATERIALS AND METHODS: The study included 100 vitiligo patients with an age range between 18 to 60 years and 100 controls with matched age, gender, and body mass index. All subjects were tested for MS components. Serum visceral adipose tissue-derived serine protease inhibitor (vaspin), fatty acid binding protein 4 (FABP4), vascular adhesion protein 1 (VAP-1), chitinase-3-like protein 1 (YKL-40), and high-sensitivity C-reactive protein (hs-CRP) were also measured. RESULTS: Regarding MS, it was observed in 22.0% of vitiligo patients and 2.0% of control subjects (P < 0.001). Serum FABP4, VAP-1, YKL-40, and hs-CRP concentrations were higher in patients than in the control group (P < 0.05 each), and their levels showed high sensitivity and specificity to differentiate MS when using the receiver operating characteristic (ROC). Levels of these markers, except serum vaspin, were significantly positively correlated with lipid profile markers (except high-density lipoprotein cholesterol) and fasting blood glucose levels (P < 0.05 each). CONCLUSION: MS was more common in vitiligo patients. The levels of the biomarkers studied were significantly higher in vitiligo patients. Furthermore, their levels accurately predicted MS in vitiligo patients. According to current research, these markers may be useful in assessing MS risk in vitiligo patients. Extensive research, however, is required. Wolters Kluwer - Medknow 2023-06-28 /pmc/articles/PMC10373801/ /pubmed/37521222 http://dx.doi.org/10.4103/idoj.idoj_674_22 Text en Copyright: © 2023 Indian Dermatology Online Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Mustafa, Amany I.
Hamed, Ahmed M.
Kadah, Ahmed S.
Fawzy, Eman M.
El Shimi, Ola S.
A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo
title A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo
title_full A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo
title_fullStr A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo
title_full_unstemmed A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo
title_short A Notorious Trio! Inflammation, Metabolic Syndrome and Vitiligo
title_sort notorious trio! inflammation, metabolic syndrome and vitiligo
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373801/
https://www.ncbi.nlm.nih.gov/pubmed/37521222
http://dx.doi.org/10.4103/idoj.idoj_674_22
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