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

被引:4
作者
Andres Salinas-Santander, Mauricio [1 ]
Baliazar Leon-Cachon, Rafael [2 ]
Cecilia Cepeda-Nieto, Ana [1 ]
Nohemi Sanchez-Dominguez, Celia [3 ]
Antonia Gonzalez-Zavala, Maria [4 ]
Leonid Gallardo-Blanco, Hugo [5 ]
Cecilia Esparza-Gonzalez, Sandra [1 ]
Angel Gonzalez-Madrazo, Miguel [1 ]
机构
[1] Autonomous Univ Coahuila, Saltillo Unit, Res Dept, Fac Med, Francisco Murguia Sur 205 Zona Ctr, Saltillo 2500, Coahuila, Mexico
[2] Univ Monterrey, Div Hlth Sci, Dept Basic Sci, San Pedro Garza Garcia 66238, Nuevo Leon, Mexico
[3] Autonomous Univ Nuevo Leon, Fac Med, Dept Biochem & Mol Med, Monterrey 64460, Nuevo Leon, Mexico
[4] Autonomous Univ Nuevo Leon, Sch Chem Sci, Saltillo 25280, Coahuila, Mexico
[5] Autonomous Univ Nuevo Leon, Sch Med, Dept Genet, Monterrey 64460, Nuevo Leon, Mexico
关键词
obesity; autoimmune diseases; inflammatory; Mexican population; PCR-RFLP; TNF alpha-308G/A; PTPN22 +1858C/T;
D O I
10.3892/br.2015.534
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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 (TNF) 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 TNF -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 TNF -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 (P0.05). 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 TNF -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.
引用
收藏
页码:107 / 111
页数:5
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