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Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population

The elongation of very long chain fatty acids (ELOVL) is a family of seven enzymes that have specific functions in the synthesis of fatty acids. Some have been shown to be related to insulin secretion (ELOVL2), and in the lipid profile (ELOVL6) and patients with various pathologies. The present work...

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Autores principales: Maycotte-Cervantes, María Luisa, Aguilar-Galarza, Adriana, Anaya-Loyola, Miriam Aracely, Anzures-Cortes, Ma. de Lourdes, Haddad-Talancón, Lorenza, Méndez-Rangel, Akram Sharim, García-Gasca, Teresa, Rodríguez-García, Víctor Manuel, Moreno-Celis, Ulisses
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694210/
https://www.ncbi.nlm.nih.gov/pubmed/33158152
http://dx.doi.org/10.3390/nu12113389
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author Maycotte-Cervantes, María Luisa
Aguilar-Galarza, Adriana
Anaya-Loyola, Miriam Aracely
Anzures-Cortes, Ma. de Lourdes
Haddad-Talancón, Lorenza
Méndez-Rangel, Akram Sharim
García-Gasca, Teresa
Rodríguez-García, Víctor Manuel
Moreno-Celis, Ulisses
author_facet Maycotte-Cervantes, María Luisa
Aguilar-Galarza, Adriana
Anaya-Loyola, Miriam Aracely
Anzures-Cortes, Ma. de Lourdes
Haddad-Talancón, Lorenza
Méndez-Rangel, Akram Sharim
García-Gasca, Teresa
Rodríguez-García, Víctor Manuel
Moreno-Celis, Ulisses
author_sort Maycotte-Cervantes, María Luisa
collection PubMed
description The elongation of very long chain fatty acids (ELOVL) is a family of seven enzymes that have specific functions in the synthesis of fatty acids. Some have been shown to be related to insulin secretion (ELOVL2), and in the lipid profile (ELOVL6) and patients with various pathologies. The present work focused on the study of ELOVL polymorphs with clinical markers of non-communicable chronic diseases in the Mexican population. A sample of 1075 participants was obtained, who underwent clinical, biochemical, and nutritional evaluation, and a genetic evaluation of 91 genetic variants of ELOVL was considered (2–7). The results indicate a 33.16% prevalence of obesity by body mass index, 13.84% prevalence of insulin resistance by homeostatic model assessment (HOMA) index, 7.85% prevalence of high cholesterol, and 20.37% prevalence of hypercholesterolemia. The deprived alleles showed that there is no association between them and clinical disease risk markers, and the notable finding of the association studies is that the ELOVL2 variants are exclusive in men and ELVOL7 in women. There is also a strong association of ELOVL6 with various markers. The present study shows, for the first time, the association between the different ELOVLs and clinical markers of chronic non-communicable diseases.
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spelling pubmed-76942102020-11-28 Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population Maycotte-Cervantes, María Luisa Aguilar-Galarza, Adriana Anaya-Loyola, Miriam Aracely Anzures-Cortes, Ma. de Lourdes Haddad-Talancón, Lorenza Méndez-Rangel, Akram Sharim García-Gasca, Teresa Rodríguez-García, Víctor Manuel Moreno-Celis, Ulisses Nutrients Article The elongation of very long chain fatty acids (ELOVL) is a family of seven enzymes that have specific functions in the synthesis of fatty acids. Some have been shown to be related to insulin secretion (ELOVL2), and in the lipid profile (ELOVL6) and patients with various pathologies. The present work focused on the study of ELOVL polymorphs with clinical markers of non-communicable chronic diseases in the Mexican population. A sample of 1075 participants was obtained, who underwent clinical, biochemical, and nutritional evaluation, and a genetic evaluation of 91 genetic variants of ELOVL was considered (2–7). The results indicate a 33.16% prevalence of obesity by body mass index, 13.84% prevalence of insulin resistance by homeostatic model assessment (HOMA) index, 7.85% prevalence of high cholesterol, and 20.37% prevalence of hypercholesterolemia. The deprived alleles showed that there is no association between them and clinical disease risk markers, and the notable finding of the association studies is that the ELOVL2 variants are exclusive in men and ELVOL7 in women. There is also a strong association of ELOVL6 with various markers. The present study shows, for the first time, the association between the different ELOVLs and clinical markers of chronic non-communicable diseases. MDPI 2020-11-04 /pmc/articles/PMC7694210/ /pubmed/33158152 http://dx.doi.org/10.3390/nu12113389 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Maycotte-Cervantes, María Luisa
Aguilar-Galarza, Adriana
Anaya-Loyola, Miriam Aracely
Anzures-Cortes, Ma. de Lourdes
Haddad-Talancón, Lorenza
Méndez-Rangel, Akram Sharim
García-Gasca, Teresa
Rodríguez-García, Víctor Manuel
Moreno-Celis, Ulisses
Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population
title Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population
title_full Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population
title_fullStr Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population
title_full_unstemmed Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population
title_short Influence of Single Nucleotide Polymorphisms of ELOVL on Biomarkers of Metabolic Alterations in the Mexican Population
title_sort influence of single nucleotide polymorphisms of elovl on biomarkers of metabolic alterations in the mexican population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694210/
https://www.ncbi.nlm.nih.gov/pubmed/33158152
http://dx.doi.org/10.3390/nu12113389
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