Identification of biological factors related to the pathological condition of postpartum depression using comprehensive epigenome analysis
Project/Area Number |
26461717
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Psychiatric science
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Research Institution | Nagoya University |
Principal Investigator |
|
Co-Investigator(Renkei-kenkyūsha) |
Ozaki Norio 名古屋大学, 医学系研究科, 教授 (40281480)
|
Project Period (FY) |
2014-04-01 – 2018-03-31
|
Project Status |
Completed (Fiscal Year 2017)
|
Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥2,860,000 (Direct Cost: ¥2,200,000、Indirect Cost: ¥660,000)
|
Keywords | 網羅的メチル化解析 / 周産期 / うつ病 / 網羅的エピゲノム解析 / DNAメチル化 |
Outline of Final Research Achievements |
In this study, we conducted comprehensive methylation analysis using peripheral blood with the aim of developing a diagnostic method for postpartum depression (PPD). A total of 18 female cases and 18 female controls were enrolled. We performed a case-control study to examine the association of DNA methylation (DNAm) status (p<1.3E-7). After that we conducted functional enrichment analysis of PPD. We observed no genome-wide significant association between the genome-wide measure of DNAm based on all CpG sites and PPD. From a result of comparing the case-control DNAm level, we selected 1,000 sites with low p-values and conducted functional enrichment analysis. As a result of enrichment analysis we found four GO Terms. From the results of this study, we confirmed that not only a single methylation site but also an analysis focusing on their functional relevance was useful for development of a diagnostic method for postpartum depression.
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Report
(5 results)
Research Products
(1 results)