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Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla

INTRODUCTION: Obesity is considered a serious public health problem. Efforts have been directed to search for candidate genes such as LEP, LEPR, and MC4R involved in the leptin- melanocortin system. The neuroendocrine regulation of these genes on energy intake and balance influences the pathogenesis...

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Autores principales: Garavito, Pilar, Mosquera-Heredia, María Isabel, Fang, Luis, Payares, Fausto, Ruiz, Marta, Arias, Isis, Tuesca, Rafael, Navarro, Édgar, Silvera-Redondo, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Nacional de Salud 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505507/
https://www.ncbi.nlm.nih.gov/pubmed/32673455
http://dx.doi.org/10.7705/biomedica.4827
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author Garavito, Pilar
Mosquera-Heredia, María Isabel
Fang, Luis
Payares, Fausto
Ruiz, Marta
Arias, Isis
Tuesca, Rafael
Navarro, Édgar
Silvera-Redondo, Carlos
author_facet Garavito, Pilar
Mosquera-Heredia, María Isabel
Fang, Luis
Payares, Fausto
Ruiz, Marta
Arias, Isis
Tuesca, Rafael
Navarro, Édgar
Silvera-Redondo, Carlos
author_sort Garavito, Pilar
collection PubMed
description INTRODUCTION: Obesity is considered a serious public health problem. Efforts have been directed to search for candidate genes such as LEP, LEPR, and MC4R involved in the leptin- melanocortin system. The neuroendocrine regulation of these genes on energy intake and balance influences the pathogenesis of this disease. Contradictory results regarding the association of these genes with obesity raise the need for new research. OBJECTIVE: To analyze the association between obesity and LEP rs2167270, LEPR rs1137101, and MC4R rs17782313 polymorphisms and the clinical and biochemical variables in obese adults from Barranquilla, Colombia. MATERIALS AND METHODS: We analyzed 111 obese adults and 155 non-obese individuals as controls. The polymorphisms were determined by real-time PCR. Besides, anthropometric measures, blood pressure, and biochemical tests were evaluated. RESULTS: No statistical differences were found in allele and genotype frequencies of gene polymorphisms between groups. The CC genotype of MC4R rs17782313 polymorphism was associated with increased systolic blood pressure and T allele and TT genotype, with decreased HDL cholesterol in obese adults. The effect of the other polymorphisms on these variables was not evidenced. CONCLUSIONS: LEP rs2167270, LEPR rs1137101, and MC4R rs17782313 polymorphisms were not associated with obesity in the population under study. MC4R rs17782313 polymorphisms were associated with an increase in systolic blood pressure and a decrease in HDL cholesterol.
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spelling pubmed-75055072020-09-22 Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla Garavito, Pilar Mosquera-Heredia, María Isabel Fang, Luis Payares, Fausto Ruiz, Marta Arias, Isis Tuesca, Rafael Navarro, Édgar Silvera-Redondo, Carlos Biomedica Artículo Original INTRODUCTION: Obesity is considered a serious public health problem. Efforts have been directed to search for candidate genes such as LEP, LEPR, and MC4R involved in the leptin- melanocortin system. The neuroendocrine regulation of these genes on energy intake and balance influences the pathogenesis of this disease. Contradictory results regarding the association of these genes with obesity raise the need for new research. OBJECTIVE: To analyze the association between obesity and LEP rs2167270, LEPR rs1137101, and MC4R rs17782313 polymorphisms and the clinical and biochemical variables in obese adults from Barranquilla, Colombia. MATERIALS AND METHODS: We analyzed 111 obese adults and 155 non-obese individuals as controls. The polymorphisms were determined by real-time PCR. Besides, anthropometric measures, blood pressure, and biochemical tests were evaluated. RESULTS: No statistical differences were found in allele and genotype frequencies of gene polymorphisms between groups. The CC genotype of MC4R rs17782313 polymorphism was associated with increased systolic blood pressure and T allele and TT genotype, with decreased HDL cholesterol in obese adults. The effect of the other polymorphisms on these variables was not evidenced. CONCLUSIONS: LEP rs2167270, LEPR rs1137101, and MC4R rs17782313 polymorphisms were not associated with obesity in the population under study. MC4R rs17782313 polymorphisms were associated with an increase in systolic blood pressure and a decrease in HDL cholesterol. Instituto Nacional de Salud 2020-06-30 /pmc/articles/PMC7505507/ /pubmed/32673455 http://dx.doi.org/10.7705/biomedica.4827 Text en https://creativecommons.org/licenses/by/4.0/ Este es un artículo publicado en acceso abierto bajo una licencia Creative Commons
spellingShingle Artículo Original
Garavito, Pilar
Mosquera-Heredia, María Isabel
Fang, Luis
Payares, Fausto
Ruiz, Marta
Arias, Isis
Tuesca, Rafael
Navarro, Édgar
Silvera-Redondo, Carlos
Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla
title Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla
title_full Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla
title_fullStr Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla
title_full_unstemmed Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla
title_short Polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de Barranquilla
title_sort polimorfismos de los genes del sistema leptina- melanocortina asociados con la obesidad en la población adulta de barranquilla
topic Artículo Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505507/
https://www.ncbi.nlm.nih.gov/pubmed/32673455
http://dx.doi.org/10.7705/biomedica.4827
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