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Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults

INTRODUCTION: The Q223R polymorphism of the leptin receptor (LEPR) gene is one of the most common polymorphisms and it is believed to be associated with a damaged capacity of LEPR signaling and with high circulating leptin levels. METHODS: An observational, cross-sectional, analytical study was carr...

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Autores principales: Diéguez-Campa, Carlos E., Angel-Chávez, Luis I., Reyes-Ruvalcaba, David, Talavera-Zermeño, María J., Armendáriz-Cabral, Diego A., Torres-Muro, Dayanara, Pérez-Neri, Iván
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Communications and Publications Division (CPD) of the IFCC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545130/
https://www.ncbi.nlm.nih.gov/pubmed/33061875
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author Diéguez-Campa, Carlos E.
Angel-Chávez, Luis I.
Reyes-Ruvalcaba, David
Talavera-Zermeño, María J.
Armendáriz-Cabral, Diego A.
Torres-Muro, Dayanara
Pérez-Neri, Iván
author_facet Diéguez-Campa, Carlos E.
Angel-Chávez, Luis I.
Reyes-Ruvalcaba, David
Talavera-Zermeño, María J.
Armendáriz-Cabral, Diego A.
Torres-Muro, Dayanara
Pérez-Neri, Iván
author_sort Diéguez-Campa, Carlos E.
collection PubMed
description INTRODUCTION: The Q223R polymorphism of the leptin receptor (LEPR) gene is one of the most common polymorphisms and it is believed to be associated with a damaged capacity of LEPR signaling and with high circulating leptin levels. METHODS: An observational, cross-sectional, analytical study was carried out in the Autonomous University of Ciudad Juarez, Mexico, where a sample of young adult participants (ranging from 18 to 30 years of age) was obtained. They were classified based on the results of body mass index: non-obese, and overweight/obese. The polymorphic variant was determined by Polymerase Chain Reaction (PCR) from the DNA sample and serum leptin levels were measured by Enzyme-Linked Immuno Sorbent Assay. RESULTS: A total of 159 participants were included (non-obese, n=103; overweight/obese, n=56). Leptin levels were 15.14±12.3 ng/mL in the non-obese group and 26.13±19.0 ng/mL in the overweight/obese group (p≤0.001). The allelic frequencies of the Q and R alleles of the LEPR gene in the studied subjects were as follows: non-obese, Q=0.56, R=0.44; overweight/obese, Q=0.62, R=0.38. The relative risk for the Q/Q genotype was 1.18 (Cl 0.53-2.34), for Q/R was 1.14 (Cl 0.59-2.18) and for R/R was 0.59 (Cl 0.23-1.50). CONCLUSIONS: This study shows that leptin levels are associated with overweight/obesity in Mexican young adults, but this is not related to the presence of the Q223R polymorphism in the LEPR gene, so the underlying mechanisms for a possible disturbance in leptin signaling in obese Mexican young adults await further studies.
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spelling pubmed-75451302020-10-14 Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults Diéguez-Campa, Carlos E. Angel-Chávez, Luis I. Reyes-Ruvalcaba, David Talavera-Zermeño, María J. Armendáriz-Cabral, Diego A. Torres-Muro, Dayanara Pérez-Neri, Iván EJIFCC Research Article INTRODUCTION: The Q223R polymorphism of the leptin receptor (LEPR) gene is one of the most common polymorphisms and it is believed to be associated with a damaged capacity of LEPR signaling and with high circulating leptin levels. METHODS: An observational, cross-sectional, analytical study was carried out in the Autonomous University of Ciudad Juarez, Mexico, where a sample of young adult participants (ranging from 18 to 30 years of age) was obtained. They were classified based on the results of body mass index: non-obese, and overweight/obese. The polymorphic variant was determined by Polymerase Chain Reaction (PCR) from the DNA sample and serum leptin levels were measured by Enzyme-Linked Immuno Sorbent Assay. RESULTS: A total of 159 participants were included (non-obese, n=103; overweight/obese, n=56). Leptin levels were 15.14±12.3 ng/mL in the non-obese group and 26.13±19.0 ng/mL in the overweight/obese group (p≤0.001). The allelic frequencies of the Q and R alleles of the LEPR gene in the studied subjects were as follows: non-obese, Q=0.56, R=0.44; overweight/obese, Q=0.62, R=0.38. The relative risk for the Q/Q genotype was 1.18 (Cl 0.53-2.34), for Q/R was 1.14 (Cl 0.59-2.18) and for R/R was 0.59 (Cl 0.23-1.50). CONCLUSIONS: This study shows that leptin levels are associated with overweight/obesity in Mexican young adults, but this is not related to the presence of the Q223R polymorphism in the LEPR gene, so the underlying mechanisms for a possible disturbance in leptin signaling in obese Mexican young adults await further studies. The Communications and Publications Division (CPD) of the IFCC 2020-09-29 /pmc/articles/PMC7545130/ /pubmed/33061875 Text en Copyright © 2020 International Federation of Clinical Chemistry and Laboratory Medicine (IFCC). All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This is a Platinum Open Access Journal distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Diéguez-Campa, Carlos E.
Angel-Chávez, Luis I.
Reyes-Ruvalcaba, David
Talavera-Zermeño, María J.
Armendáriz-Cabral, Diego A.
Torres-Muro, Dayanara
Pérez-Neri, Iván
Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults
title Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults
title_full Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults
title_fullStr Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults
title_full_unstemmed Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults
title_short Leptin Levels and Q223R Leptin Receptor Gene Polymorphism in Obese Mexican Young Adults
title_sort leptin levels and q223r leptin receptor gene polymorphism in obese mexican young adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545130/
https://www.ncbi.nlm.nih.gov/pubmed/33061875
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