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Assessment of biochemical parameters and characterization of TNFα -308G/A and PTPN22 +1858c/T gene polymorphisms in the risk of obesity in adolescents

  • Mauricio Andrés Salinas-Santander
    ,
  • ,
  • Ana Cecilia Cepeda-Nieto
    ,
  • Celia Nohemí Sánchez-Domínguez
    ,
  • María Antonia González-Zavala
    ,
  • Hugo Leonid Gallardo-Blanco
  • Universidad Autonoma de Coahuila
    ,
  • Universidad Autonoma de Nuevo Leon
Research Output: Contribution to journal Article Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

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SciVal
FWCI
0.17
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Author count
8
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Citations
5
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Paper percentile
36
Scopus
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Abstract

Obesity is currently considered an inflammatory condition associated with autoimmune diseases, suggesting a common origin. Among other factors, candidate genes may explain the development of this disease. Polymorphisms in the tumor necrosis factor α (TNFα) and lymphoid protein tyrosine phosphatase (PTPN22) genes lead to an increased risk to development of immune and inflammatory diseases. The aim of the present study was to analyze the biochemical parameters and the effect of the TNFα -308G/A and PTPN22 +1858C/T polymorphisms in the susceptibility of adolescents to obesity. A group of 253 adolescent subjects were recruited and classified as obese, overweight or normal weight according to their nutritional status. Anthropometric measurements, clinical and biochemical data were analyzed. DNA was extracted from peripheral blood samples by the phenol-chloroform method, and TNFα -308G/A and PTPN22 1858C/T polymorphisms were determined by polymerase chain reaction-restriction fragment length polymorphism assays. Clinical, genetic and biochemical parameters were analyzed to determine the existence of a possible association with the development of obesity. Statistically significant differences in body mass index, insulin, triglyceride levels and homeostatic model assessment for insulin resistance (HOMA-IR) index were observed among the three groups analyzed (P≤0.05). The studied polymorphisms did not confer a risk for developing obesity in the analyzed population (P>0.05); however, significantly low levels of insulin and decreased rates of HOMA-IR were observed in the 1858 CT genotype carriers of the PTPN22 gene. In conclusion, no association between the TNFα -308G/A and PTPN22 +1858C/T polymorphisms and the risk to development of obesity in the adolescent population analyzed was observed. However, the 1858 CT genotype of the PTPN22 gene was associated with variations of certain biochemical parameters analyzed.

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 107-111 (5 pages)

Journal (Volume, Issue Number)

Biomedical Reports (Volume 4, Issue 1)

Publication milestones

  • Published - 01/01/2016

Publication status

Published - 01/01/2016

ISSN

2049-9434

Publication IDs

  • Scopus: 85046242403
  • PubMed: 26870345