Epigenome-wide association study detects a novel loci associated with central obesity in healthy subjects

Central obesity is a condition that poses a significant risk to global health and requires the employment of novel scientific methods for exploration. The objective of this study is to use DNA methylation analysis to detect DNA methylation loci linked to obesity phenotypes, i.e. waist circumference...

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Veröffentlicht in:BMC medical genomics 2021-09, Vol.14 (1), p.233-8, Article 233
Hauptverfasser: Xie, Ting, Gorenjak, Vesna, Stathopoulou, Maria G, Dadé, Sébastien, Marouli, Eirini, Masson, Christine, Murray, Helena, Lamont, John, Fitzgerald, Peter, Deloukas, Panos, Visvikis-Siest, Sophie
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Sprache:eng
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Zusammenfassung:Central obesity is a condition that poses a significant risk to global health and requires the employment of novel scientific methods for exploration. The objective of this study is to use DNA methylation analysis to detect DNA methylation loci linked to obesity phenotypes, i.e. waist circumference and waist-to-hip ratio adjusted for BMI. Two-hundred and ten healthy European participants from the STANISLAS Family Study (SFS), comprising 73 nuclear families, were comprehensively assessed for methylation status using Illumina Infinium HumanMethylation450 BeadChip. An epigenome-wide association study was performed, which identified a CpG site cg16170243 located on chromosome 18q21.2 significantly associated with waist circumference, after adjusting for BMI (β = 2.32, SE = 0.41, P  = 0.048). Cg16170243 corresponds to a 50 bp-length human methylation oligoprobe located within the AC090241.2 gene that overlaps ST8SIA5 gene. No significant association was observed with waist-to-hip ratio adjusted for BMI (P  > 0.05). A novel association between DNA methylation and WC was identified, which is demonstrating that epigenetic mechanisms may have a significant impact on waist circumference ratio in healthy individuals. Further studies are warranted to address the causal effects of this association.
ISSN:1755-8794
1755-8794
DOI:10.1186/s12920-021-01077-9