Epigenetic Determinants of Major Depression: a Monozygotic Discordant Twin Study

重度抑郁症的表观遗传决定因素：同卵不一致双胞胎研究

• 批准号: 8503945
• 负责人: Andrew James Sharp
• 金额: $ 64.71万
• 依托单位: TULANE UNIVERSITY OF LOUISIANA
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-08-15 至 2018-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8503945
• 关键词: Aberrant DNA Methylation; Adult; Affect; American; Amygdaloid structure; Area; Authorization documentation; Autopsy; Belief; Biological; Blood; Brain; Brain region; Candidate Disease Gene; Classification; Collection; Communities; Complex; CpG Islands; DNA; DNA Methylation; Data; Depressed mood; Diagnosis; Diagnostic; Disease; Early Diagnosis; Enrollment; Environmental Risk Factor; Epigenetic Process; Functional disorder; Gene Expression; Gene Expression Profile; Genes; Genetic; Genomics; Goals; Hippocampus (Brain); Knowledge; Link; Major Depressive Disorder; Medical Research; Mental Depression; Mental disorders; Messenger RNA; Methylation; Modification; Monozygotic Twinning; Monozygotic twins; Organ; Outcome; Pathogenesis; Pathway interactions; Patients; Play; Prevention; Preventive; Preventive Intervention; Procedures; Recruitment Activity; Registries; Research; Research Institute; Risk; Risk Assessment; Risk Factors; Role; Sampling; Technology; Therapeutic; Therapeutic Intervention; Tissues; Twin Multiple Birth; Twin Studies; Uncertainty; Universities; Variant; Washington; Work; base; bisulfite; brain tissue; cingulate cortex; design; disorder control; disorder risk; epigenetic marker; epigenetic variation; epigenome; frontal lobe; genome-wide; interest; monocyte; novel; promoter; psychogenetics; public health relevance; pyrosequencing; research study; therapeutic target

DESCRIPTION (provided by applicant): Major depressive disorder (MDD) is a devastating psychiatric disorder that affects millions of Americans. Despite substantial research, no specific risk factor has yet been identified as having a causal role in MDD. Epigenetic modifications, especially DNA methylation, are increasingly being recognized as a key mechanism involved in the pathogenesis of depression. However, the biological pathways linking aberrant methylation to depression remain poorly understood. This uncertainty greatly hampers our ability to implement early diagnosis, prevention and treatment for this debilitating disorder. The objective of this study is to identify functional epigenetic determinants for MDD. Our central hypothesis is that aberrant DNA methylation and resulting alterations in gene expression are associated with MDD. The rationale for the proposed research is that: once we know the epigenetic determinants for depression, we will be able to develop novel epigenetic markers and therapeutic targets for risk assessment, prevention and treatment of MDD and related psychiatric conditions. We proposed three specific aims: (1) Identify differentially methylated regions (DMRs) associated with MDD. This aim is to conduct an epigenome-wide DNA methylation analysis to identify epigenetic variations contributing to MDD in monocytes DNA from 100 monozygotic (MZ) discordant twin pairs from the University of Washington Twin Registry (UWTR), a large community-based twin registry in the U.S. (2) Replicate the top 50 ranked genes from Aim 1 in two independent samples, including 80 MZ discordant twin pairs recruited from the same registry and 36 postmortem brain tissue of well-characterized MDD patients and matched controls. (3) Determine the functional importance of the positive methylation findings in both blood and brain by profiling gene expression levels in each of the four brain regions (frontal cortex, hippocampus, amygdala, and cingulate cortex). Differential expressed genes related to MDD will be identified. Integrative analyses will be performed to elucidate the connections between DNA methylation patterns and gene expression of cognate genes in relation to MDD. The proposed study is the only one of its kind to identify functional epigenetic determinants for MDD in a well- matched MZ discordant twin sample, followed by replication in postmortem brain tissue, the affected organ in MDD. The work proposed here is expected to have an important positive impact, because genes with both differential methylation and expression are highly likely to provide novel epigenetic targets for prevention, intervention and treatment for depression and its related psychiatric conditions in addition to fundamentally advancing the fields of psychiatric genetics.

描述（由申请人提供）：重度抑郁症（MDD）是一种影响数百万美国人的毁灭性精神疾病。尽管有大量的研究，但尚未确定特定的风险因素在MDD中具有因果作用。表观遗传修饰，特别是DNA甲基化，越来越多地被认为是参与抑郁症发病机制的关键机制。然而，将异常甲基化与抑郁症联系起来的生物学途径仍然知之甚少。这种不确定性极大地阻碍了我们对这种使人衰弱的疾病进行早期诊断、预防和治疗的能力。本研究的目的是确定MDD的功能表观遗传决定因素。我们的中心假设是，异常的DNA甲基化和基因表达的改变与MDD相关。这项研究的基本原理是：一旦我们知道抑郁症的表观遗传决定因素，我们将能够开发新的表观遗传标记和治疗靶点，用于风险评估，预防和治疗MDD和相关精神疾病。我们提出了三个具体的目标：（1）识别与MDD相关的差异甲基化区域（DMR）。该目的是进行表观基因组范围的DNA甲基化分析，以鉴定来自华盛顿大学双胞胎登记处（UWTR）（美国一个大型的基于社区的双胞胎登记处）的100对单卵（MZ）不一致双胞胎对的单核细胞DNA中促成MDD的表观遗传变异。（2）在两个独立样品中复制来自Aim 1的前50个排名基因，包括从同一登记处招募的80对MZ不一致双胞胎和36例特征明确的MDD患者和匹配对照的死后脑组织。(3)通过分析四个大脑区域（额叶皮层、海马、杏仁核和扣带皮层）中每个区域的基因表达水平，确定血液和大脑中阳性甲基化结果的功能重要性。将鉴定与MDD相关的差异表达基因。将进行综合分析，以阐明与MDD相关的同源基因的DNA甲基化模式和基因表达之间的联系。这项拟议的研究是同类研究中唯一一项在匹配良好的MZ不一致双胞胎样本中鉴定MDD的功能性表观遗传决定因素，然后在死后脑组织（MDD的受影响器官）中复制。这里提出的工作预计将产生重要的积极影响，因为具有差异甲基化和表达的基因极有可能为预防，干预和治疗抑郁症及其相关精神疾病提供新的表观遗传靶点，此外还从根本上推进了精神遗传学领域。