The role of FTO variant rs1421085 in the relationship with obesity: a systematic review and meta-analysis.

Eat Weight Disord

Cellular and Molecular Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, No 24, Parvaneh St, Yemen St, Chamran Exp, PO Box 1985717413, Tehran, Iran.

Published: December 2022

AI Article Synopsis

  • The study focuses on the FTO gene's variant rs1421085, which has been linked to obesity risk, though some previous research has shown inconsistent results.
  • A systematic review and meta-analysis evaluated studies from multiple databases and analyzed data from 5,169 obese individuals and 7,772 non-obese individuals to assess the relationship between rs1421085 and obesity.
  • The findings confirmed that the rs1421085 variant significantly increases the risk of obesity across various genetic models, showing a strong positive association to the condition.

Article Abstract

Purpose: Fat mass and obesity-associated (FTO) is considered the first locus associated with adiposity, a concerning health problem worldwide. Many studies have evaluated the relationship between the FTO variants and obesity susceptibility. While the strong association of FTO rs1421085 with the risk of obesity across populations was reported in different studies, some researchers found a lack of association of this variant with adiposity. This systematic review and meta-analysis aimed to assess the association between obesity and rs1421085 polymorphism.

Methods: We systematically searched PubMed, Scopus, and Google Scholar up to June 2022 to find pertinent studies. To further assess this issue, we surveyed the probable association of rs1421085 with obesity development among Iranian adults using the logistic regression analysis, and the obtained results were used for doing meta-analysis. After selection, nine eligible studies were included in the meta-analysis through the random- and fixed-effect models to determine the combined odds ratios (OR) and 95% confidence intervals (CI).

Results: According to our meta-analysis conducted on 5169 obese and 7772 non-obese individuals using different genetic models, including recessive, dominant, over-dominant, and additive, rs1421085 could positively increase the risk of obesity under all tested genetic models. Also, we detected a high to moderate level of heterogeneity among different studies under various genetic models.

Conclusion: This meta-analysis further verified the positive association of FTO rs1421085 with the risk of developing obesity.

Study Registration: This study is registered as PROSPERO CRD42021220092.

Level Of Evidence: Level I, systematic reviews and meta-analyses.

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Source
http://dx.doi.org/10.1007/s40519-022-01509-0DOI Listing

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