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Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris

BACKGROUND: Vitiligo is a common depigmented skin disorder characterised by the selective destruction of melanocytes. AIMS AND OBJECTIVES: This study aimed to assess serum desnutrin and its association with insulin resistance in patients with vitiligo vulgaris. MATERIALS AND METHODS: This study was...

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Autores principales: El-Hamd, Mohammed Abu, Sedky, Ahmed, Mahmoud, Asmaa B., Abd El-Magid, Wafaa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564220/
https://www.ncbi.nlm.nih.gov/pubmed/37822413
http://dx.doi.org/10.4103/ijd.ijd_435_22
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author El-Hamd, Mohammed Abu
Sedky, Ahmed
Mahmoud, Asmaa B.
Abd El-Magid, Wafaa M.
author_facet El-Hamd, Mohammed Abu
Sedky, Ahmed
Mahmoud, Asmaa B.
Abd El-Magid, Wafaa M.
author_sort El-Hamd, Mohammed Abu
collection PubMed
description BACKGROUND: Vitiligo is a common depigmented skin disorder characterised by the selective destruction of melanocytes. AIMS AND OBJECTIVES: This study aimed to assess serum desnutrin and its association with insulin resistance in patients with vitiligo vulgaris. MATERIALS AND METHODS: This study was a cross-sectional case-control study. It included 45 patients with vitiligo vulgaris and 45 age- and sex-matched healthy controls. Patients were subjected to complete general and cutaneous evaluations. All participants were subjected to the assay of fasting blood glucose (FBG), cholesterol, triglyceride, high-density lipoprotein (HDL), very low-density lipoprotein (VLDL), low-density lipoprotein (LDL), fasting serum insulin and serum desnutrin. Homeostasis Model Assessment + insulin resistance (HOMA + IR) was calculated for all participants. RESULTS: There were statistically significant differences between the patients with vitiligo vulgaris and healthy controls regarding HDL, FBG, fasting insulin, HOMA-IR, and serum desnutrin (P < 0.001). Desnutrin levels were negatively correlated with FBS, LDL, VLDL, fasting insulin, and HOMA-IR (P < 0.05). Unlikely, the level of desnutrin had a positive, non-significant correlation with HDL (rho = 0.17, P = 0.059). CONCLUSION: This study concluded that in patients with vitiligo vulgaris, as a result of increased serum levels of glucose and insulin, the serum desnutrin was suppressed, perhaps contributing to hyperlipidaemia and IR. So, low serum desnutrin could be a biomarker for IR in patients with vitiligo vulgaris. A multidisciplinary approach is essential for the early detection of diabetes mellitus, IR and hyperlipidemia among patients with vitiligo vulgaris to avoid cardiovascular and metabolic complications.
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spelling pubmed-105642202023-10-11 Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris El-Hamd, Mohammed Abu Sedky, Ahmed Mahmoud, Asmaa B. Abd El-Magid, Wafaa M. Indian J Dermatol Original Article BACKGROUND: Vitiligo is a common depigmented skin disorder characterised by the selective destruction of melanocytes. AIMS AND OBJECTIVES: This study aimed to assess serum desnutrin and its association with insulin resistance in patients with vitiligo vulgaris. MATERIALS AND METHODS: This study was a cross-sectional case-control study. It included 45 patients with vitiligo vulgaris and 45 age- and sex-matched healthy controls. Patients were subjected to complete general and cutaneous evaluations. All participants were subjected to the assay of fasting blood glucose (FBG), cholesterol, triglyceride, high-density lipoprotein (HDL), very low-density lipoprotein (VLDL), low-density lipoprotein (LDL), fasting serum insulin and serum desnutrin. Homeostasis Model Assessment + insulin resistance (HOMA + IR) was calculated for all participants. RESULTS: There were statistically significant differences between the patients with vitiligo vulgaris and healthy controls regarding HDL, FBG, fasting insulin, HOMA-IR, and serum desnutrin (P < 0.001). Desnutrin levels were negatively correlated with FBS, LDL, VLDL, fasting insulin, and HOMA-IR (P < 0.05). Unlikely, the level of desnutrin had a positive, non-significant correlation with HDL (rho = 0.17, P = 0.059). CONCLUSION: This study concluded that in patients with vitiligo vulgaris, as a result of increased serum levels of glucose and insulin, the serum desnutrin was suppressed, perhaps contributing to hyperlipidaemia and IR. So, low serum desnutrin could be a biomarker for IR in patients with vitiligo vulgaris. A multidisciplinary approach is essential for the early detection of diabetes mellitus, IR and hyperlipidemia among patients with vitiligo vulgaris to avoid cardiovascular and metabolic complications. Wolters Kluwer - Medknow 2023 /pmc/articles/PMC10564220/ /pubmed/37822413 http://dx.doi.org/10.4103/ijd.ijd_435_22 Text en Copyright: © 2023 Indian Journal of Dermatology 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
El-Hamd, Mohammed Abu
Sedky, Ahmed
Mahmoud, Asmaa B.
Abd El-Magid, Wafaa M.
Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris
title Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris
title_full Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris
title_fullStr Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris
title_full_unstemmed Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris
title_short Desnutrin as a Biomarker for Insulin Resistance in Patients with Vitiligo Vulgaris
title_sort desnutrin as a biomarker for insulin resistance in patients with vitiligo vulgaris
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564220/
https://www.ncbi.nlm.nih.gov/pubmed/37822413
http://dx.doi.org/10.4103/ijd.ijd_435_22
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