表观遗传学
DNA甲基化
精神分裂症(面向对象编程)
生物
遗传学
生物信息学
基因
医学
基因表达
精神科
作者
Thabo Magwai,Khanyiso Bright Shangase,Fredrick Otieno Oginga,Bonginkosi Chiliza,Thabisile Mpofana,Khethelo Richman Xulu
出处
期刊:Cells
[MDPI AG]
日期:2021-10-26
卷期号:10 (11): 2890-2890
被引量:38
标识
DOI:10.3390/cells10112890
摘要
Schizophrenia is a neuropsychiatric disorder characterized by dissociation of thoughts, idea, identity, and emotions. It has no central pathophysiological mechanism and precise diagnostic markers. Despite its high heritability, there are also environmental factors implicated in the development of schizophrenia. Epigenetic factors are thought to mediate the effects of environmental factors in the development of the disorder. Epigenetic modifications like DNA methylation are a risk factor for schizophrenia. Targeted gene approach studies attempted to find candidate gene methylation, but the results are contradictory. Genome-wide methylation studies are insufficient in literature and the available data do not cover different populations like the African populations. The current genome-wide studies have limitations related to the sample and methods used. Studies are required to control for these limitations. Integration of DNA methylation, gene expression, and their effects are important in the understanding of the development of schizophrenia and search for biomarkers. There are currently no precise and functional biomarkers for the disorder. Several epigenetic markers have been reported to be common in functional and peripheral tissue. This makes the peripheral tissue epigenetic changes a surrogate of functional tissue, suggesting common epigenetic alteration can be used as biomarkers of schizophrenia in peripheral tissue.
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