Wu Yujia, Chen Yun, Chen Bo, Wu Wenjuan, Yang Jiankang
School of Basic Medical Sciences, Dali University, Dali, China.
Department of Dermatology, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Front Med (Lausanne). 2023 Jul 24;10:1196149. doi: 10.3389/fmed.2023.1196149. eCollection 2023.
Acne is a chronic inflammatory skin disease that affects the pilosebaceous follicle and is influenced by heredity, hormones, inflammation, and the environment. At present, the recognized pathogenesis mainly includes four categories: excessive sebum secretion, excessive proliferation, excessive keratinization of sebaceous glands in hair follicles, and inflammatory mechanisms. Previous studies have found that DNA methylation is closely related to some chronic inflammatory skin diseases, and there is evidence that DNA methylation is controlled by genetic factors, making us want to know the relationship between DNA methylation, genetic variation and acne.
In our previous study, we performed genome-wide DNA methylation analysis in peripheral blood samples from 44 patients with severe acne and 44 unaffected normal subjects, and identified 23 differentially methylated probes (DMPs). In this study, we identified single nucleotide polymorphisms (SNPs) associated with severe acne by genome-wide association analysis in these 88 samples. To test the association between SNPs and DMPs, we conducted DNA methylation quantitative trait loci (methQTL) analysis. Next, causal inference testing (CIT) was used to determine whether genetic variation influences DNA methylation, which impacts disease phenotypes.
We found 38,269 SNPs associated with severe acne. By methQTL analysis, we obtained 24 SNP-CpG pairs that reached the threshold (FDR < 0.05), which included 7 unique CpGs and 22 unique methQTL SNPs. After CIT analysis, we found that 11 out of 24 pairs of SNP-CpG showed a weakened SNP effect after adjustment for methylation, indicating a methylation-mediated relationship between SNPs and severe acne. These 11 SNP-CpG pairs consist of four unique CpG sites and 11 SNPs, of which three CpG sites, cg03020863, cg20652636, and cg19964325, are located on the gene body of PDGFD, the intron of SH2D6, and the 5'UTR of the IL1R1 gene, respectively.
During this study, the DNA methylation of certain genes was found to be influenced by genetic factors and mediated the risk of severe acne in a young Chinese male population, providing a new perspective on the pathogenesis of severe acne.
痤疮是一种影响毛囊的慢性炎症性皮肤病,受遗传、激素、炎症和环境影响。目前,公认的发病机制主要包括四类:皮脂分泌过多、过度增殖、毛囊皮脂腺过度角化以及炎症机制。先前的研究发现,DNA甲基化与一些慢性炎症性皮肤病密切相关,并且有证据表明DNA甲基化受遗传因素控制,这促使我们想了解DNA甲基化、基因变异与痤疮之间的关系。
在我们之前的研究中,我们对44例重度痤疮患者和44例未受影响的正常受试者的外周血样本进行了全基因组DNA甲基化分析,并鉴定出23个差异甲基化探针(DMP)。在本研究中,我们通过对这88个样本进行全基因组关联分析,鉴定出与重度痤疮相关的单核苷酸多态性(SNP)。为了测试SNP与DMP之间的关联,我们进行了DNA甲基化定量性状位点(methQTL)分析。接下来,使用因果推断测试(CIT)来确定基因变异是否影响DNA甲基化,进而影响疾病表型。
我们发现了38269个与重度痤疮相关的SNP。通过methQTL分析,我们获得了24对达到阈值(FDR < 0.05)的SNP-CpG对,其中包括7个独特的CpG和22个独特的methQTL SNP。经过CIT分析,我们发现24对SNP-CpG中的11对在调整甲基化后显示出减弱的SNP效应,表明SNP与重度痤疮之间存在甲基化介导的关系。这11对SNP-CpG由4个独特的CpG位点和11个SNP组成,其中三个CpG位点,即cg03020863、cg20652636和cg19964325,分别位于PDGFD的基因体、SH2D6的内含子和IL1R1基因的5'UTR上。
在本研究中,发现某些基因的DNA甲基化受遗传因素影响,并介导了中国年轻男性人群中重度痤疮的风险,为重度痤疮的发病机制提供了新的视角。