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No association of adiponectin +45 T/G polymorphism with the risk of gestational diabetes mellitus: Evidence from a meta-analysis

INTRODUCTION: Adiponectin (ADIPOQ), involved in regulating glucose levels and fatty acid oxidation, plays key roles in metabolic derangements such as gestational diabetes mellitus (GDM). Previously, several studies have been conducted to assess the association between ADIPOQ +45 T/G polymorphism and...

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Detalles Bibliográficos
Autores principales: Xu, Fang, Zhang, Hua, Qi, Hongbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843878/
https://www.ncbi.nlm.nih.gov/pubmed/27296394
http://dx.doi.org/10.1177/1470320316653283
Descripción
Sumario:INTRODUCTION: Adiponectin (ADIPOQ), involved in regulating glucose levels and fatty acid oxidation, plays key roles in metabolic derangements such as gestational diabetes mellitus (GDM). Previously, several studies have been conducted to assess the association between ADIPOQ +45 T/G polymorphism and risk of GDM. The results, however, are inconclusive. We aimed to evaluate the effect of the polymorphism on the risk of GDM using a meta-analysis. MATERIALS AND METHODS: After databases searching, eight records were identified. Pooled odds ratios (ORs) with their corresponding 95% confidence intervals (CIs) were used to evaluate the association between ADIPOQ +45 T/G polymorphism and risk of GDM. RESULTS: No significant association was observed between the ADIPOQ +45 T/G polymorphism and the risk of GDM (heterozygote comparison: OR = 1.15, 95% CI, 0.70–1.89; homozygote comparison: OR = 1.21, 95% CI, 0.48–3.03; dominant model: OR = 0.86, 95% CI, 0.50–1.48, recessive model: OR = 1.21, 95% CI, 0.62–2.33, and allele comparison: OR = 1.17, 95% CI, 0.79–1.76, respectively). Apparent heterogeneity was detected. However, no evidence of publication bias was found. CONCLUSIONS: This meta-analysis provides evidence that the ADIPOQ +45 T/G polymorphism was not related to the risk of GDM. Further multicenter, prospective studies with larger sample size would be valuable to confirm the result.