Evidence from a meta-analysis for association of MC4R rs17782313 and FTO rs9939609 polymorphisms with susceptibility to obesity in children

Diabetes Metab Syndr. 2021 Sep-Oct;15(5):102234. doi: 10.1016/j.dsx.2021.102234. Epub 2021 Jul 30.

Abstract

Background and aim: The aim of this study was to evaluate the association of MC4R rs17782313 and FTO rs9939609 polymorphisms with childhood obesity.

Methods: A universal search was performed up to May 2021.

Results: A total of 31 studies including 13 studies with 9565 cases and 11956 controls on MC4R rs17782313 and 18 studies with 4789 cases and 15918 controls on FTO rs9939609 were selected.

Conclusions: Pooled data showed that FTO rs9930506 and MC4R rs17782313 polymorphisms were significantly associated with obesity in children. Stratified analyses revealed that these genetic variants were associated with childhood obesity in Caucasian and Asian children.

Keywords: Children; Fat mass and obesity associated gene; Melanocortin-4 receptor gene; Obesity; Polymorphism.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO / genetics*
  • Child
  • Genetic Predisposition to Disease*
  • Humans
  • Pediatric Obesity / etiology
  • Pediatric Obesity / metabolism
  • Pediatric Obesity / pathology*
  • Polymorphism, Single Nucleotide*
  • Prognosis
  • Receptor, Melanocortin, Type 4 / genetics*

Substances

  • MC4R protein, human
  • Receptor, Melanocortin, Type 4
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • FTO protein, human