Genome-wide DNA methylation in 1-year-old infants of mothers with major depressive disorder.
Genome-wide DNA methylation in 1-year-old infants of mothers with major depressive disorder.
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DOI:
10.1017/s0954579416000912
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发表时间:
2016-11
影响因子:
3.3
通讯作者:
Toth SL
中科院分区:
文献类型:
--
作者:
Cicchetti D;Hetzel S;Rogosch FA;Handley ED;Toth SL
A genome-wide methylation study was conducted among a sample of 114 infants (M age = 13.2 mo.; SD = 1.08) of low-income urban women with (n=73) and without (n=41) Major Depressive Disorder (MDD). The Illumina HumanMethylation450 BeadChip array with the GenomeStudio Methylation Module and Illumina Custom model were used to conduct differential methylation analyses. Using the 5.0 × 10−7 p-value, 2119 loci were found to be significantly different between infants of depressed and non-depressed mothers. Infants of depressed mothers had greater methylation at low methylation sites (0–29%) compared to infants of non-depressed mothers. At high levels of methylation (70–100%) the infants of depressed mothers were predominantly hypomethylated. The mean difference in methylation between the infants of depressed and infants of non-depressed mothers was 5.23%. Disease by biomarker analyses were also conducted using GeneGo MetaCore Software. Results indicated significant cancer-related differences in biomarker networks such as prostatic neoplasms, ovarian and breast neoplasms, and colonic neoplasms. Results of a process networks analysis indicated significant differences in process networks associated with neuronal development and central nervous system functioning, as well as cardiac development between infants of depressed and non-depressed mothers. These findings indicate that early in development, infants of mothers with MDD evince epigenetic differences relative to infants of well mothers that suggest risk for later adverse health outcomes.