Department of Rheumatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands
Department of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Ann Rheum Dis. 2019 Sep;78(9):1198-1204. doi: 10.1136/annrheumdis-2018-214930. Epub 2019 May 29.
The main objective of this study was to determine whether the DNA methylation profile of children born to mothers with rheumatoid arthritis (RA) is different from that of children born to mothers from the general population. In addition, we aimed to determine whether any differences in methylation are associated with maternal RA disease activity or medication use during pregnancy.
For this study, genome-wide DNA methylation was measured at cytosine-phosphate-guanine (CpG) sites, using the Infinium Illumina HumanMethylation 450K BeadChip, in 80 blood samples from children (mean age=6.8 years) born to mothers with RA. As controls, blood samples from 354 children (mean age=6.0 years) from the population-based Generation R Study were used. Linear mixed models were performed to investigate differential methylation between the groups, corrected for relevant confounders.
A total of 147 CpGs were differentially methylated between blood samples of children born to mothers with RA and the control blood samples. The five most significantly associated CpGs were cg06642177, cg08867893, cg06778273, cg07786668 and cg20116574. The differences in methylation were not associated with maternal RA disease activity or medication use during pregnancy.
DNA methylation at 147 CpGs differed between children born to mothers with RA and children born to mothers from the general population. It remains unknown whether the identified associations are causal, and if so whether they are caused by the disease or treatment. More research, including replication of these results, is necessary in order to strengthen the relevance of our findings for the later-life health of children born to mothers with RA.
本研究的主要目的是确定患有类风湿关节炎(RA)的母亲所生儿童的 DNA 甲基化谱是否与普通人群母亲所生儿童的甲基化谱不同。此外,我们还旨在确定母体 RA 疾病活动或孕期用药是否与任何甲基化差异相关。
在这项研究中,我们使用 Infinium Illumina HumanMethylation 450K BeadChip 测量了 80 名儿童(平均年龄=6.8 岁)的血液样本中的全基因组 DNA 甲基化,这些儿童的母亲患有 RA。作为对照,使用了来自基于人群的 Generation R 研究的 354 名儿童(平均年龄=6.0 岁)的血液样本。为了调查两组之间的差异甲基化,我们进行了线性混合模型分析,并对相关混杂因素进行了校正。
RA 母亲所生儿童与对照血液样本之间存在 147 个差异甲基化的 CpG。与差异甲基化最显著相关的 5 个 CpG 是 cg06642177、cg08867893、cg06778273、cg07786668 和 cg20116574。甲基化的差异与母体 RA 疾病活动或孕期用药无关。
RA 母亲所生儿童与普通人群母亲所生儿童的 DNA 甲基化在 147 个 CpG 处存在差异。尚不清楚所确定的关联是否具有因果关系,如果是,它们是由疾病还是治疗引起的。为了加强我们的研究结果与 RA 母亲所生儿童后期健康的相关性,需要进行更多的研究,包括对这些结果的复制。