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MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients
This study was performed for investigation the relationship between variants of MTP gene polymorphism and the development of NAFLD in patients with and without MS. The study was included 174 NAFLD patients (106 with MS and 68 without MS), and 141 healthy control subjects. The 493 G/T polymorphism of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chongqing Medical University
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147179/ https://www.ncbi.nlm.nih.gov/pubmed/30258926 http://dx.doi.org/10.1016/j.gendis.2017.09.002 |
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author | Gouda, Weaam Ashour, Esmat Shaker, Yehia Ezzat, Wafaa |
author_facet | Gouda, Weaam Ashour, Esmat Shaker, Yehia Ezzat, Wafaa |
author_sort | Gouda, Weaam |
collection | PubMed |
description | This study was performed for investigation the relationship between variants of MTP gene polymorphism and the development of NAFLD in patients with and without MS. The study was included 174 NAFLD patients (106 with MS and 68 without MS), and 141 healthy control subjects. The 493 G/T polymorphism of MTP gene was evaluated by PCR-RFLP method. The frequency of MTP TT genotype and T allele were significantly higher in NAFLD patients when compared to healthy controls. Moreover, a significant association in MTP gene polymorphism was observed in NAFLD patients with MS compared to NAFLD patients without MS and controls. Our study suggested that MTP 493 G/T gene polymorphism may act as susceptibility biomarker for NAFLD and MS. |
format | Online Article Text |
id | pubmed-6147179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Chongqing Medical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-61471792018-09-26 MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients Gouda, Weaam Ashour, Esmat Shaker, Yehia Ezzat, Wafaa Genes Dis Article This study was performed for investigation the relationship between variants of MTP gene polymorphism and the development of NAFLD in patients with and without MS. The study was included 174 NAFLD patients (106 with MS and 68 without MS), and 141 healthy control subjects. The 493 G/T polymorphism of MTP gene was evaluated by PCR-RFLP method. The frequency of MTP TT genotype and T allele were significantly higher in NAFLD patients when compared to healthy controls. Moreover, a significant association in MTP gene polymorphism was observed in NAFLD patients with MS compared to NAFLD patients without MS and controls. Our study suggested that MTP 493 G/T gene polymorphism may act as susceptibility biomarker for NAFLD and MS. Chongqing Medical University 2017-10-16 /pmc/articles/PMC6147179/ /pubmed/30258926 http://dx.doi.org/10.1016/j.gendis.2017.09.002 Text en © 2017 Chongqing Medical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Gouda, Weaam Ashour, Esmat Shaker, Yehia Ezzat, Wafaa MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients |
title | MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients |
title_full | MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients |
title_fullStr | MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients |
title_full_unstemmed | MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients |
title_short | MTP genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients |
title_sort | mtp genetic variants associated with non-alcoholic fatty liver in metabolic syndrome patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147179/ https://www.ncbi.nlm.nih.gov/pubmed/30258926 http://dx.doi.org/10.1016/j.gendis.2017.09.002 |
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