AI Article Synopsis

  • The study investigates the relationship between mitochondrial DNA (mtDNA) variants and obesity risk in Kuwaiti and Qatari populations, to address the high obesity prevalence in these regions.
  • Analysis of whole exome sequencing data from 1,112 participants identified haplogroup R as having a protective effect against obesity, with statistically significant results even after adjusting for age and sex.
  • While several mtDNA variants showed initial associations with obesity, they lost significance after further testing; the findings suggest haplogroup R could serve as a biomarker for obesity risk, warranting more research for confirmation.

Article Abstract

Background: The Kuwaiti and Qatari populations have a high prevalence of obesity, a major risk factor for various metabolic disorders. Previous studies have independently explored mitochondrial DNA (mtDNA) variations and their association with obesity in these populations. This study aims to investigate the role of mtDNA haplogroups and variants in obesity risk among these Gulf populations.

Methods: Whole exome sequencing data from 1,112 participants (348 Kuwaitis and 764 Qataris) were analyzed for mtDNA variants. Participants were classified as obese or non-obese based on body mass index (BMI). Association analyses were performed to examine the relationship between mtDNA haplogroups and obesity, adjusting for covariates such as age and sex.

Results: Haplogroup R was found to be protective against obesity, with an odds ratio (OR) of 0.69 (p = 0.045). This association remained significant after adjusting for age and sex (OR = 0.694; 95% CI: 0.482-0.997; p = 0.048). Several mtDNA variants, particularly those involved in mitochondrial energy metabolism, showed nominal associations with obesity, but these did not remain significant after correcting for multiple testing.

Conclusion: Haplogroup R consistently demonstrates a protective association against obesity in both Kuwaiti and Qatari populations, highlighting its potential as a biomarker for obesity risk in the Gulf region. However, further research with larger sample sizes is needed to validate these findings and clarify the role of mtDNA variants in obesity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11502345PMC
http://dx.doi.org/10.3389/fendo.2024.1449374DOI Listing

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