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dc.contributor.authorMartínez Martínez, María D.
dc.contributor.authorMendieta Zerón, Hugo
dc.contributor.authorCelis Regalado, Luis Gustavo
dc.contributor.authorLayton Tovar, Cristian F.
dc.contributor.authorTorres García, Rocío
dc.contributor.authorGutiérrez Pliego, Laura E.
dc.contributor.authorCamarillo Romero, Eneida
dc.contributor.authorGarduño García, José D.
dc.contributor.authorCamarillo Romero, María D.
dc.date.accessioned8/2/2020 10:41
dc.date.available2020-08-02T15:41:00Z
dc.date.issued2018-03-13
dc.identifier.otherhttps://journals.squ.edu.om/index.php/squmj/article/view/2848
dc.identifier.otherhttps://journals.squ.edu.om/index.php/squmj/article/view/2848/2512
dc.identifier.urihttp://hdl.handle.net/10818/42619
dc.description8 páginases_CO
dc.description.abstractObjectives: This study aimed to describe correlations between glucose, insulin and adipokine levels and the homeostasis model assessment (HOMA) index with regards to the presence/absence of fat mass and obesity-associated (FTO) rs9939609 and peroxisome proliferator-activated receptor (PPAR)-y rs1801282 single nucleotide polymorphisms (SNPs) as indicators of body mass index in adolescents. Methods: This cross-sectional study was conducted between September and December 2016 in Toluca, Mexico. A total of 71 students between 14–18 years old were included. Various anthropometric and laboratory measurements were collected, including lipid profile, glucose, insulin and adipokine levels and HOMA index. The degree of association between variables was evaluated with regards to the presence/absence of the SNPs. Results: Leptin levels were significantly higher among female students (P = 0.001), although adiponectin levels did not differ significantly (P = 0.060). There were significant positive correlations between insulin levels and HOMA index with FTO (r = 0.391; P = 0.007 and r = 0.413; P = 0.005, respectively) and PPARγ (r = 0.529; P = 0.007 and r = 0.537; P = 0.007, respectively) SNPs. Leptin showed a significant positive correlation in the presence of PPARγ (r = 0.483; P = 0.007) or in the absence of both SNPs (r = 0.627; P = 0.039). However, adiponectin was significantly negatively correlated in the presence of FTO, either alone (r = −0.333; P = 0.024) or in combination with PPARγ (r = −0.616; P = 0.043). Conclusion: The presence of FTO and/or PPARγ SNPs might be related to a genetic predisposition to metabolic syndrome.en
dc.formatapplication/pdfes_CO
dc.language.isoenges_CO
dc.publisherSQU Medical Journales_CO
dc.relation.ispartofseriesSQU Medical Journal, August 2018, Volume 18, Issue 3
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceUniversidad de La Sabanaes_CO
dc.sourceIntellectum Repositorio Universidad de La Sabanaes_CO
dc.subjectObesityes_CO
dc.subjectBody Mass Indexes_CO
dc.subjectSingle Nucleotide Polymorphismses_CO
dc.subjectFat Mass and Obesity Associated Proteines_CO
dc.subjectHumanes_CO
dc.subjectPeroxisome Proliferator-Activated Receptor gammaes_CO
dc.subjectAdipokineses_CO
dc.titleCorrelation of the Homeostasis Model Assessment Index and Adiponectin, Leptin and Insulin Levels to Body Mass Index-Associated Gene Polymorphisms in Adolescentses_CO
dc.typearticleen
dc.type.hasVersionpublishedVersiones_CO
dc.rights.accessRightsopenAccesses_CO
dc.identifier.doi10.18295/squmj.2018.18.03.005


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