精神障碍中催产素受体(OXTR)甲基化与认知

Tyler B. Grove, K. Burghardt, A. Kraal, Ryan J. Dougherty, S. Taylor, V. Ellingrod
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引用次数: 14

摘要

以前的报告已经确定了精神疾病中认知障碍和遗传变异之间的联系。特别是,这种关联可能与负责广泛认知功能的基因如催产素受体(OXTR)的异常调节有关。在精神疾病中,对于基因调控具有重要意义的OXTR甲基化是否与认知功能有关尚不清楚。目前的研究检查了精神分裂症、分裂情感性障碍和精神障碍患者外周血OXTR甲基化和一般认知(N = 101)。通过分层多元回归分析,在控制多重测试的情况下,Chr3:8767638位点的甲基化与复合认知能力显著相关,独立于人口统计学和药物因素(调整p = 0.023)。
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Oxytocin Receptor (OXTR) Methylation and Cognition in Psychotic Disorders
Previous reports have identified an association between cognitive impairment and genetic variation in psychotic disorders. In particular, this association may be related to abnormal regulation of genes responsible for broad cognitive functions such as the oxytocin receptor (OXTR). Within psychotic disorders, it is unknown if OXTR methylation, which can have important implications for gene regulation, is related to cognitive function. The current study examined peripheral blood OXTR methylation and general cognition in people with schizophrenia, schizoaffective disorder, and psychotic disorder not otherwise specified (N = 101). Using hierarchical multiple regression analysis, methylation at the Chr3:8767638 site was significantly associated with composite cognitive performance independent of demographic and medication factors while controlling for multiple testing in this combined diagnostic sample (adjusted p = 0.023).
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