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Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients
INTRODUCTION: Isotretinoin, a vitamin A-derived medication, is one of the effective treatments for severe acne. However, in a fraction of patients, this treatment causes significant adverse effects. Leptin is a pro-inflammatory cytokine that plays a role in apoptosis of adipose cells and sebaceous l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973407/ https://www.ncbi.nlm.nih.gov/pubmed/29872305 http://dx.doi.org/10.2147/TCRM.S165712 |
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author | Khabour, Omar F Alzoubi, Karem H Firoz, Abdul Samad Al-Awad, Rafat MM |
author_facet | Khabour, Omar F Alzoubi, Karem H Firoz, Abdul Samad Al-Awad, Rafat MM |
author_sort | Khabour, Omar F |
collection | PubMed |
description | INTRODUCTION: Isotretinoin, a vitamin A-derived medication, is one of the effective treatments for severe acne. However, in a fraction of patients, this treatment causes significant adverse effects. Leptin is a pro-inflammatory cytokine that plays a role in apoptosis of adipose cells and sebaceous lipid metabolism. Thus, genetic polymorphisms in the leptin (LEP) gene may modulate the response to isotretinoin therapy. Here, we explore the contribution of rs7799039 polymorphism of the LEP gene in the adverse effects of the oral isotretinoin therapy among acne patients. MATERIALS AND METHODS: Clinical parameters were obtained from 200 patients before and after isotretinoin treatment for acne. In addition, circulatory lipid profile and aspartate transaminase (AST) and alanine aminotransferase (ALT) enzymes from acne subjects before and 1 month after oral isotretinoin treatment were also measured. RESULTS: An association between the rs7799039 polymorphism and the following lipid parameters: high-density lipoprotein (HDL) at baseline and after treatment, HDL % change, low-density lipoprotein % change and total cholesterol % change (P < 0.05). In addition, there was an association between the LEP polymorphism and higher AST and ALT at baseline and after treatment (P < 0.05). CONCLUSION: In conclusion, rs7799039 LEP polymorphism might modulate lipid parameters and liver enzymes, but not other major side effects of oral isotretinoin therapy. |
format | Online Article Text |
id | pubmed-5973407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59734072018-06-05 Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients Khabour, Omar F Alzoubi, Karem H Firoz, Abdul Samad Al-Awad, Rafat MM Ther Clin Risk Manag Original Research INTRODUCTION: Isotretinoin, a vitamin A-derived medication, is one of the effective treatments for severe acne. However, in a fraction of patients, this treatment causes significant adverse effects. Leptin is a pro-inflammatory cytokine that plays a role in apoptosis of adipose cells and sebaceous lipid metabolism. Thus, genetic polymorphisms in the leptin (LEP) gene may modulate the response to isotretinoin therapy. Here, we explore the contribution of rs7799039 polymorphism of the LEP gene in the adverse effects of the oral isotretinoin therapy among acne patients. MATERIALS AND METHODS: Clinical parameters were obtained from 200 patients before and after isotretinoin treatment for acne. In addition, circulatory lipid profile and aspartate transaminase (AST) and alanine aminotransferase (ALT) enzymes from acne subjects before and 1 month after oral isotretinoin treatment were also measured. RESULTS: An association between the rs7799039 polymorphism and the following lipid parameters: high-density lipoprotein (HDL) at baseline and after treatment, HDL % change, low-density lipoprotein % change and total cholesterol % change (P < 0.05). In addition, there was an association between the LEP polymorphism and higher AST and ALT at baseline and after treatment (P < 0.05). CONCLUSION: In conclusion, rs7799039 LEP polymorphism might modulate lipid parameters and liver enzymes, but not other major side effects of oral isotretinoin therapy. Dove Medical Press 2018-05-23 /pmc/articles/PMC5973407/ /pubmed/29872305 http://dx.doi.org/10.2147/TCRM.S165712 Text en © 2018 Khabour et al. 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. |
spellingShingle | Original Research Khabour, Omar F Alzoubi, Karem H Firoz, Abdul Samad Al-Awad, Rafat MM Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients |
title | Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients |
title_full | Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients |
title_fullStr | Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients |
title_full_unstemmed | Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients |
title_short | Association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients |
title_sort | association between leptin gene rs7799039 polymorphism and lipid profile changes induced by isotretinoin treatment in acne patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973407/ https://www.ncbi.nlm.nih.gov/pubmed/29872305 http://dx.doi.org/10.2147/TCRM.S165712 |
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