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Association of Obesity Susceptibility Gene Variants with Metabolic Syndrome and Related Traits in 1,443 Czech Adolescents

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    0396556 - BTÚ 2014 RIV CZ eng J - Journal Article
    Dusatkova, L. - Zamrazilova, H. - Sedlackova, B. - Vcelak, J. - Hlavaty, P. - Hainerova, I.A. - Korenková, Vlasta - Bradnova, O. - Bendlova, B. - Kunesova, M. - Hainer, V.
    Association of Obesity Susceptibility Gene Variants with Metabolic Syndrome and Related Traits in 1,443 Czech Adolescents.
    Folia Biologica. Roč. 59, č. 3 (2013), s. 123-133. ISSN 0015-5500. E-ISSN 0015-5500
    Institutional research plan: CEZ:AV0Z50520701
    Keywords : Genome-wide association studies * obesity * metabolic syndrome
    Subject RIV: EB - Genetics ; Molecular Biology
    Impact factor: 1.167, year: 2013

    Genome-wide association studies have revealed several gene variants associated with obesity; however, only a few studies have further investigated their association with metabolic syndrome. We performed a study of eleven variants in/near genes TMEM18, SH2B1, KCTD15, PCSK1, BDNF, SEC16B, MC4R, and FTO in Czech adolescents and analysed their association with obesity, metabolic syndrome and related traits. Genotyping was performed in 1,443 adolescents aged 13.0-17.9 years. Anthropometric parameters, biochemical parameters and blood pressure were assessed. Metabolic syndrome was defined according to the International Diabetes Federation. The FTO rs9939609 variant was associated with overweight/obesity (OR 1.40, 95% Cl 1.21-1.63, P < 0.001). The minor allele of TMEM18 rs7561317 was related to underweight (OR 1.78, 95% CI 1.14-2.79, P = 0.015). BDNF rs925946 and MC4R rs17782313 were associated with metabolic syndrome (OR 1.53, 95% CI 1.14-2.04, P = 0.005; 1.51, 95% CI 1.12-2.04, P = 0.009). The PCSK1 rs6235 variant was negatively related to increased blood glucose (OR 0.69,95% CI 0.49-0.97, P = 0.040). In conclusion, the FTO variant was associated with overweight/obesity in Czech adolescents. Moreover, MC4R and BDNF variants increased the risk of metabolic syndrome, probably through their effect on abdominal obesity. The PCSK1 variant may have a protective role in the development of type 2 diabetes.
    Permanent Link: http://hdl.handle.net/11104/0224343

     
     
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