Rubin Leah H, Connelly Jessica J, Reilly James L, Carter C Sue, Drogos Lauren L, Pournajafi-Nazarloo Hossein, Ruocco Anthony C, Keedy Sarah K, Matthew Ian, Tandon Neeraj, Pearlson Godfrey D, Clementz Brett A, Tamminga Carol A, Gershon Elliot S, Keshavan Matcheri S, Bishop Jeffrey R, Sweeney John A
Department of Psychiatry, University of Illinois at Chicago, Chicago, IL.
Department of Psychology, University of Virginia, Charlottesville, VA.
Biol Psychiatry Cogn Neurosci Neuroimaging. 2016 Mar 1;1(2):141-151. doi: 10.1016/j.bpsc.2015.10.003. Epub 2015 Nov 9.
The oxytocin (OT) system, including receptor epigenetic mechanisms, has been shown to influence emotion processing, especially in females. Whether OT receptor () epigenetic alterations occur across psychotic disorders in relation to illness-related disturbances in social cognition and brain anatomy is unknown.
Participants with affective and nonaffective psychotic disorders (92 women, 75 men) and healthy controls (38 women, 37 men) from the Chicago site of the BSNIP study completed the Penn Emotion Recognition Test (ER-40), a facial emotion recognition task. We measured cytosine methylation at site -934 upstream of the start codon in DNA from whole blood, and for the first time their relationship with plasma OT levels assessed by enzyme-immunoassay. Volumes of brain regions supporting social cognition were measured from MRI scans using FreeSurfer.
Patients with prototypic schizophrenia features showed higher levels of DNA methylation than those with prototypic bipolar features. Methylation was higher in women than men, and was associated with poorer emotion recognition only in female patients and controls. Greater methylation was associated with smaller volumes in temporal-limbic and prefrontal regions associated previously with social cognition, but only in healthy women and females with schizophrenia.
DNA methylation of the site -934 was higher in schizophrenia spectrum than bipolar patients. Among patients, it was linked to behavioral deficits in social cognition and neuroanatomic structures known to support emotion processing only in schizophrenia spectrum individuals.
包括受体表观遗传机制在内的催产素(OT)系统已被证明会影响情绪处理,尤其是在女性中。OT受体()表观遗传改变是否会在整个精神障碍中出现,与社会认知和脑解剖结构中与疾病相关的紊乱有关,目前尚不清楚。
来自BSNIP研究芝加哥站点的患有情感性和非情感性精神障碍的参与者(92名女性,75名男性)以及健康对照者(38名女性,37名男性)完成了面部表情识别任务——宾夕法尼亚情绪识别测试(ER - 40)。我们测量了全血DNA中起始密码子上游 - 934位点的胞嘧啶甲基化情况,并首次测量了其与通过酶免疫测定法评估的血浆OT水平之间的关系。使用FreeSurfer从MRI扫描中测量支持社会认知的脑区体积。
具有典型精神分裂症特征的患者比具有典型双相情感障碍特征的患者表现出更高水平的DNA甲基化。女性的甲基化水平高于男性,并且仅在女性患者和对照者中与较差的情绪识别相关。更高的甲基化与先前与社会认知相关的颞叶边缘和前额叶区域的较小体积相关,但仅在健康女性和患有精神分裂症的女性中如此。
精神分裂症谱系患者中 - 934位点的DNA甲基化高于双相情感障碍患者。在患者中,它与社会认知方面的行为缺陷以及仅在精神分裂症谱系个体中已知支持情绪处理的神经解剖结构有关。