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Type 2 diabetes-associated genetic variants of FTO, LEPR, PPARg, and TCF7L2 in gestational diabetes in a Brazilian population
Anghebem-Oliveira, Mauren Isfer; Martins, Bruna Rodrigues; Alberton, Dayane; Ramos, Edneia Amancio de Souza; Picheth, Geraldo; Rego, Fabiane Gomes de Moraes.
  • Anghebem-Oliveira, Mauren Isfer; Universidade Federal do Paraná. Departamento de Análises Clínicas. Curitiba. BR
  • Martins, Bruna Rodrigues; Universidade Federal do Paraná. Departamento de Análises Clínicas. Curitiba. BR
  • Alberton, Dayane; Universidade Federal do Paraná. Departamento de Análises Clínicas. Curitiba. BR
  • Ramos, Edneia Amancio de Souza; Universidade Federal do Paraná. Departamento de Análises Clínicas. Curitiba. BR
  • Picheth, Geraldo; Universidade Federal do Paraná. Departamento de Análises Clínicas. Curitiba. BR
  • Rego, Fabiane Gomes de Moraes; Universidade Federal do Paraná. Departamento de Análises Clínicas. Curitiba. BR
Arch. endocrinol. metab. (Online) ; 61(3): 238-248, May-June 2017. tab, graf
Article in English | LILACS | ID: biblio-887551
ABSTRACT
ABSTRACT Objective Gestational diabetes mellitus (GDM) is a metabolic disorder that shares pathophysiologic features with type 2 diabetes mellitus. The aim of this study was to investigate the association of the polymorphisms fat mass and obesity-associated (FTO) rs1421085, leptin receptor (LEPR) rs1137100, rs1137101, peroxisome proliferator-activated receptor gamma (PPARg) rs1801282, and transcription factor 7-like 2 (TCF7L2) rs7901695 with GDM. Subjects and methods 252 unrelated Euro-Brazilian pregnant women were classified into two groups according to the 2015 criteria of the American and Brazilian Diabetes Association healthy pregnant women (n = 125) and pregnant women with GDM (n = 127), matched by age. The polymorphisms were genotyped using fluorescent probes (TaqMan®). Results All groups were in Hardy-Weinberg equilibrium. The genotype and allele frequencies of the studied polymorphisms did not show significant differences between the groups (P > 0.05). In the healthy and GDM groups, the C allele frequencies (95% CI) of the FTO rs1421085 polymorphism were 36.8% [31-43%] and 35.0% [29-41%]; the G allele frequencies (95% CI) of the LEPR rs1137100 polymorphism were 24.8% [19-30%] and 22.8% [18-28%]; the G allele frequencies (95% CI) of the LEPR rs1137101 polymorphism were 43.6% [37-50%] and 42.9% [37-49%]; the G allele frequencies (95% CI) of the PPARg rs1801282 polymorphism were 7.6% [4-11%] and 8.3% [5-12%]; and the C allele frequencies (95% CI) of the TCF7L2 rs7901695 polymorphism were 33.6% [28-39%] and 39.0% [33-45%], respectively. Conclusion The studied polymorphisms were not associated with GDM in a Brazilian population.
Subject(s)


Full text: Available Index: LILACS (Americas) Main subject: Polymorphism, Genetic / Diabetes, Gestational / PPAR gamma / Diabetes Mellitus, Type 2 / Receptors, Leptin / Transcription Factor 7-Like 2 Protein / Alpha-Ketoglutarate-Dependent Dioxygenase FTO Type of study: Etiology study / Observational study / Prevalence study / Prognostic study / Risk factors Limits: Adult / Female / Humans Country/Region as subject: South America / Brazil Language: English Journal: Arch. endocrinol. metab. (Online) Journal subject: Endocrinology / Metabolism Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Paraná/BR

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Full text: Available Index: LILACS (Americas) Main subject: Polymorphism, Genetic / Diabetes, Gestational / PPAR gamma / Diabetes Mellitus, Type 2 / Receptors, Leptin / Transcription Factor 7-Like 2 Protein / Alpha-Ketoglutarate-Dependent Dioxygenase FTO Type of study: Etiology study / Observational study / Prevalence study / Prognostic study / Risk factors Limits: Adult / Female / Humans Country/Region as subject: South America / Brazil Language: English Journal: Arch. endocrinol. metab. (Online) Journal subject: Endocrinology / Metabolism Year: 2017 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal do Paraná/BR