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Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women

INTRODUCTION: Melasma is a condition of hyperpigmentation of the facial skin that increases in prevalence with ageing. The alleged involvement of reactive oxygen species and antioxidants is the basis of the pathology of melasma. Glutathione is one of the non-enzymatic antioxidants produced by the bo...

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Autores principales: Wiraguna, Anak Agung Gde Putra, Hari, Embun Dini, Praharsini, I Gusti Ayu Agung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367920/
https://www.ncbi.nlm.nih.gov/pubmed/32765038
http://dx.doi.org/10.2147/CCID.S258834
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author Wiraguna, Anak Agung Gde Putra
Hari, Embun Dini
Praharsini, I Gusti Ayu Agung
author_facet Wiraguna, Anak Agung Gde Putra
Hari, Embun Dini
Praharsini, I Gusti Ayu Agung
author_sort Wiraguna, Anak Agung Gde Putra
collection PubMed
description INTRODUCTION: Melasma is a condition of hyperpigmentation of the facial skin that increases in prevalence with ageing. The alleged involvement of reactive oxygen species and antioxidants is the basis of the pathology of melasma. Glutathione is one of the non-enzymatic antioxidants produced by the body and plays a role in melanogenesis. The purpose of this study was to examine serum glutathione levels on the severity of melasma. METHODS: This study used a cross-sectional design conducted at the Cosmetic Dermatology Clinic at Sanglah Hospital, Denpasar, from September to October 2016. Serum glutathione was examined through venous blood with ELISA method, and the severity of melasma was assessed using melasma area severity index (MASI). Independent t-test and ANOVA were used to evaluate differences in plasma glutathione levels based on the characteristics of the sample. Pearson correlation test and linear regression were used to assess the relationship between MASI and plasma glutathione. RESULTS: This study involved 47 people with a clinical diagnosis of melasma. There was a significant strong negative correlation between plasma glutathione and MASI (p<0.001; r = −0.624). Mild melasma (1.89 ± 0.28 µmol/L) had higher plasma glutathione levels compared to moderate melasma (1.53 ± 0.13 µmol/L) and severe (1.18 ± 0.20 µmol/L) (p=0.043). Linear regression showed a significant negative linear relationship between MASI scores against plasma glutathione (β = −58.2; p <0.01). CONCLUSION: Glutathione plasma has a strong negative correlation with the MASI score in person with melasma.
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spelling pubmed-73679202020-08-05 Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women Wiraguna, Anak Agung Gde Putra Hari, Embun Dini Praharsini, I Gusti Ayu Agung Clin Cosmet Investig Dermatol Original Research INTRODUCTION: Melasma is a condition of hyperpigmentation of the facial skin that increases in prevalence with ageing. The alleged involvement of reactive oxygen species and antioxidants is the basis of the pathology of melasma. Glutathione is one of the non-enzymatic antioxidants produced by the body and plays a role in melanogenesis. The purpose of this study was to examine serum glutathione levels on the severity of melasma. METHODS: This study used a cross-sectional design conducted at the Cosmetic Dermatology Clinic at Sanglah Hospital, Denpasar, from September to October 2016. Serum glutathione was examined through venous blood with ELISA method, and the severity of melasma was assessed using melasma area severity index (MASI). Independent t-test and ANOVA were used to evaluate differences in plasma glutathione levels based on the characteristics of the sample. Pearson correlation test and linear regression were used to assess the relationship between MASI and plasma glutathione. RESULTS: This study involved 47 people with a clinical diagnosis of melasma. There was a significant strong negative correlation between plasma glutathione and MASI (p<0.001; r = −0.624). Mild melasma (1.89 ± 0.28 µmol/L) had higher plasma glutathione levels compared to moderate melasma (1.53 ± 0.13 µmol/L) and severe (1.18 ± 0.20 µmol/L) (p=0.043). Linear regression showed a significant negative linear relationship between MASI scores against plasma glutathione (β = −58.2; p <0.01). CONCLUSION: Glutathione plasma has a strong negative correlation with the MASI score in person with melasma. Dove 2020-07-09 /pmc/articles/PMC7367920/ /pubmed/32765038 http://dx.doi.org/10.2147/CCID.S258834 Text en © 2020 Wiraguna et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wiraguna, Anak Agung Gde Putra
Hari, Embun Dini
Praharsini, I Gusti Ayu Agung
Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women
title Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women
title_full Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women
title_fullStr Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women
title_full_unstemmed Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women
title_short Correlation Between Glutathione Plasma with Degree Severity of Melasma in Balinese Women
title_sort correlation between glutathione plasma with degree severity of melasma in balinese women
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367920/
https://www.ncbi.nlm.nih.gov/pubmed/32765038
http://dx.doi.org/10.2147/CCID.S258834
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