Lee Jangho, Choi Hyo-Kyoung, Park Soo-Hyun, Lee Yu Geon, Park Jae-Ho
Korea Food Research Institute, Jeollabuk-do, 55365, Jeollabuk-do, Republic of Korea.
Sci Rep. 2025 Aug 6;15(1):28681. doi: 10.1038/s41598-025-13868-6.
Obesity and abdominal obesity contribute to significant metabolic health risks through distinct pathophysiological mechanisms. We conducted an epigenome-wide association study to identify differential DNA methylation patterns associated with body mass index (BMI)-defined and abdominal obesity and explore their relationships with dietary intake among Korean adults (n = 1,526). We identified 23 and 1931 DMPs associated with abdominal obesity and severe BMI-defined obesity, respectively, with four CpG sites common to both phenotypes. The most significant associations were at cg10323433 and cg10501210 in serotonin receptor 2 A (HTR2A) for abdominal obesity (Δβ = -0.023) and BMI-defined obesity (Δβ = -0.021), respectively. Most DMPs (> 75%) exhibited hypomethylation in obesity with progressive changes correlating with obesity severity. Hierarchical clustering revealed distinct dietary associations: WHR-related DMPs correlated with traditional fermented foods, whereas BMI-related DMPs showed stronger associations with fruit consumption. Sites with hypomethylation in obesity consistently demonstrated positive correlations with fat intake but negative correlations with carbohydrates. The distinct associations between methylation patterns and dietary components suggest that different foods may influence epigenetic modifications that are specific to overall adiposity or fat distribution, providing potential targets for nutritional interventions to modify obesity-related epigenetic signatures.
肥胖和腹型肥胖通过不同的病理生理机制导致显著的代谢健康风险。我们进行了一项全表观基因组关联研究,以确定与体重指数(BMI)定义的肥胖和腹型肥胖相关的差异DNA甲基化模式,并探讨它们与韩国成年人(n = 1526)饮食摄入之间的关系。我们分别鉴定出与腹型肥胖和严重BMI定义的肥胖相关的23个和1931个差异甲基化位点(DMP),两种表型共有四个CpG位点。最显著的关联分别是腹型肥胖在血清素受体2A(HTR2A)中的cg10323433和cg10501210(Δβ = -0.023),以及BMI定义的肥胖中的(Δβ = -0.021)。大多数DMP(>75%)在肥胖中表现为低甲基化,且随着肥胖严重程度的增加呈现渐进性变化。层次聚类揭示了不同的饮食关联:与腰臀比(WHR)相关的DMP与传统发酵食品相关,而与BMI相关的DMP与水果消费的关联更强。肥胖中低甲基化的位点始终与脂肪摄入呈正相关,但与碳水化合物呈负相关。甲基化模式与饮食成分之间的不同关联表明,不同的食物可能会影响特定于总体肥胖或脂肪分布的表观遗传修饰,为营养干预以改变肥胖相关的表观遗传特征提供了潜在靶点。