Connor Caroline M, Akbarian Schahram
Program in Neurobiology, Graduate School of Biomedical Sciences, Department of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts 01604, USA.
Epigenetics. 2008 Mar-Apr;3(2):55-8. doi: 10.4161/epi.3.2.5938. Epub 2008 Mar 19.
The etiology of the major psychotic disorders, including schizophrenia and bipolar disorder, remains poorly understood. Postmortem brain studies have revealed altered expression of multiple mRNAs, affecting neurotransmission, metabolism, myelination and other functions. Epigenetic mechanisms could be involved, because for a limited number of genes, the alterations of mRNA levels have been linked to inverse DNA methylation changes at sites of the corresponding promoters. However, results from independent studies have been inconsistent, and when expressed in quantitative terms, disease-related methylation changes appear to be comparatively subtle. A recent study identified approximately 100 loci with altered CpG methylation in schizophrenia or bipolar disorder, the majority of which were gender-specific. Additional work will be necessary to clarify the origin and timing of these methylation changes in psychosis and to determine the specific cell types affected in the diseased brain.
包括精神分裂症和双相情感障碍在内的主要精神障碍的病因仍未得到充分理解。死后大脑研究显示多种mRNA的表达发生改变,影响神经传递、代谢、髓鞘形成及其他功能。表观遗传机制可能与之相关,因为对于少数基因,mRNA水平的改变已与相应启动子位点的DNA甲基化反向变化相关联。然而,独立研究的结果并不一致,而且从定量角度来看,疾病相关的甲基化变化似乎相对细微。最近一项研究在精神分裂症或双相情感障碍中鉴定出约100个CpG甲基化改变的位点,其中大多数是性别特异性的。需要进一步开展工作以阐明这些精神病甲基化变化的起源和时间,并确定患病大脑中受影响的具体细胞类型。