| Literature DB >> 29305581 |
Mihoko Shimada1,2, Takeshi Otowa3, Taku Miyagawa1,2, Tadashi Umekage4, Yoshiya Kawamura5, Miki Bundo6, Kazuya Iwamoto6, Tempei Ikegame7, Mamoru Tochigi8, Kiyoto Kasai7, Hisanobu Kaiya9, Hisashi Tanii10, Yuji Okazaki11, Katsushi Tokunaga2, Tsukasa Sasaki12.
Abstract
Major depressive disorder is a common psychiatric disorder that is thought to be triggered by both genetic and environmental factors. Depressive symptoms are an important public health problem and contribute to vulnerability to major depression. Although a substantial number of genetic and epigenetic studies have been performed to date, the detailed etiology of depression remains unclear and there are no validated biomarkers. DNA methylation is one of the major epigenetic modifications that play diverse roles in the etiology of complex diseases. In this study, we performed an epigenome-wide association study (EWAS) of DNA methylation on subjects with (N = 20) or without (N = 27) depressive symptoms in order to examine whether different levels of DNA methylation were associated with depressive tendencies. Employing methylation-array technology, a total of 363,887 methylation sites across the genomes were investigated and several candidate CpG sites associated with depressive symptoms were identified, especially annotated to genes linked to a G-protein coupled receptor protein signaling pathway. These data provide a strong impetus for validation studies using a larger cohort and support the possibility that G-protein coupled receptor protein signaling pathways are involved in the pathogenesis of depression.Entities:
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Year: 2018 PMID: 29305581 DOI: 10.1038/s10038-017-0382-y
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172