Medical Department III-Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, Germany.
Helmholtz Institute for Metabolic, Obesity and Vascular Research (HI-MAG), Helmholtz Zentrum München, University of Leipzig and University Hospital Leipzig, Leipzig, Germany.
Clin Transl Med. 2022 Jun;12(6):e851. doi: 10.1002/ctm2.851.
Obesity is driven by modifiable lifestyle factors whose effects may be mediated by epigenetics. Therefore, we investigated lifestyle effects on blood DNA methylation in participants of the LIFE-Adult study, a well-characterised population-based cohort from Germany.
Lifestyle scores (LS) based on diet, physical activity, smoking and alcohol intake were calculated in 4107 participants of the LIFE-Adult study. Fifty subjects with an extremely healthy lifestyle and 50 with an extremely unhealthy lifestyle (5th and 95th percentiles LS) were selected for genome-wide DNA methylation analysis in blood samples employing Illumina Infinium® Methylation EPIC BeadChip system technology.
Differences in DNA methylation patterns between body mass index groups (<25 vs. >30 kg/m ) were rather marginal compared to inter-lifestyle differences (0 vs. 145 differentially methylated positions [DMPs]), which identified 4682 differentially methylated regions (DMRs; false discovery rate [FDR <5%) annotated to 4426 unique genes. A DMR annotated to the glutamine-fructose-6-phosphate transaminase 2 (GFPT2) locus showed the strongest hypomethylation (∼6.9%), and one annotated to glutamate rich 1 (ERICH1) showed the strongest hypermethylation (∼5.4%) in healthy compared to unhealthy lifestyle individuals. Intersection analysis showed that diet, physical activity, smoking and alcohol intake equally contributed to the observed differences, which affected, among others, pathways related to glutamatergic synapses (adj. p < .01) and axon guidance (adj. p < .05). We showed that methylation age correlates with chronological age and waist-to-hip ratio with lower DNA methylation age (DNAmAge) acceleration distances in participants with healthy lifestyles. Finally, two identified top DMPs for the alanyl aminopeptidase (ANPEP) locus also showed the strongest expression quantitative trait methylation in blood.
DNA methylation patterns help discriminate individuals with a healthy versus unhealthy lifestyle, which may mask subtle methylation differences derived from obesity.
肥胖是由可改变的生活方式因素驱动的,其影响可能受到表观遗传学的调节。因此,我们在德国一项基于人群的 LIFE-Adult 研究中,研究了生活方式对血液 DNA 甲基化的影响。
在 LIFE-Adult 研究的 4107 名参与者中,基于饮食、体力活动、吸烟和饮酒摄入计算了生活方式评分(LS)。选择 50 名生活方式非常健康的个体和 50 名生活方式非常不健康的个体(LS 的第 5 和 95 百分位数),采用 Illumina Infinium® Methylation EPIC BeadChip 系统技术,对血液样本进行全基因组 DNA 甲基化分析。
与生活方式差异(0 与 145 个差异甲基化位置[DMP])相比,体重指数组(<25 与>30kg/m )之间的 DNA 甲基化模式差异相当微小,鉴定出 4682 个差异甲基化区域(DMR;错误发现率[FDR<5%]注释到 4426 个独特基因。在健康生活方式个体中,谷氨酰胺果糖-6-磷酸转氨酶 2(GFPT2)基因座注释的 DMR 表现出最强的去甲基化(约 6.9%),而谷氨酸丰富 1(ERICH1)基因座注释的 DMR 表现出最强的超甲基化(约 5.4%)。交集分析表明,饮食、体力活动、吸烟和饮酒摄入同样促成了所观察到的差异,这些差异影响了与谷氨酰胺能突触(adj.p<.01)和轴突导向(adj.p<.05)相关的途径等。我们表明,甲基化年龄与实际年龄相关,腰围与臀围比与健康生活方式参与者的 DNA 甲基化年龄(DNAmAge)加速距离相关。最后,两个鉴定的位于丙氨酰氨基肽酶(ANPEP)基因座的 topDMP 也显示了血液中最强的表达数量性状甲基化。
DNA 甲基化模式有助于区分生活方式健康与不健康的个体,这可能掩盖了肥胖导致的微妙甲基化差异。