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Association between UCP polymorphisms and adipokines with obesity in Mexican adolescents

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Published/Copyright: April 10, 2018

Abstract

Background:

It has been reported that the uncoupling proteins (UCPs) can contribute to energy metabolism, and are thus involved in the pathogenesis of obesity. The objective of the study was to analyze the association between UCP polymorphisms, clinical parameters and leptin and adiponectin plasma levels in an adolescent population with overweight and obesity.

Methods:

We analyzed the UCP1 -3826 C/T, UCP2-866 G/A, Ala55Val and UCP3 -55 C/T polymorphisms and the levels of adipokines in adolescents with normal weight and with overweight or obesity. The study included 270 students aged between 12 and 18 years categorized according to the percentiles from Mexico City. Adipokines levels were measured by immunoassay methods and the UCP polymorphisms were determined using Taqman real-time polymerase chain reaction (RT-PCR).

Results:

No significant differences were found in the UCP polymorphisms in seven inheritance models studied. Most of the significant differences in the clinical parameters were found under a recessive model, the UCP2 -866 polymorphism was associated with diastolic blood pressure (p=0.008), triglycerides (p=0.045), low-density lipoprotein-cholesterol (LDL-C) (p=0.003), high-density lipoprotein-cholesterol (HDL-C) (p=0.050) and plasma levels of leptin (p<0.001). Also, the obese group was found to have higher leptin levels and lower adiponectin levels in GA+AA vs. GG (recessive model).

Conclusions:

This study demonstrated a direct relationship between the clinical characteristics and UCP2-866 in a recessive model, associated with high levels of leptin and decreased levels of adiponectin in an obese or overweight Mexican adolescent population.

Acknowledgments

The authors thank the participants of this study.

  1. Author contributions: R. Sámano, R. Gamboa and designed the study; R. Sámano, C. Huesca-Gómez, R. López-Marure A. Rodríguez-Ventura, AK. Hernandez-Cabrera and M. Tolentino collected the data; R. Sámano, R. Gamboa, C. Huesca-Gómez and A. Rodríguez-Ventura contributed to data analysis and interpretation; R. Gamboa drafted the manuscript. All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: Funding for this study was provided by Instituto Nacional de Perinatología in the public sector, Funder Id: 10.13039/501100007686, registry 212250-49541 and Consejo Nacional de Ciencia y Tecnología, project number 179967 CB2012-01.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2017-7-4
Accepted: 2018-2-5
Published Online: 2018-4-10
Published in Print: 2018-5-24

©2018 Walter de Gruyter GmbH, Berlin/Boston

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