Gene expression of methylation cycle and related genes in lymphocytes and brain of patients with schizophrenia and non-psychotic controls

Q2 Medicine
Henry Sershen , Alessandro Guidotti , James Auta , Jenny Drnevich , Dennis R. Grayson , Marin Veldic , Jordan Meyers , Mary Youseff , Adrian Zhubi , Keturah Faurot , Renrong Wu , Jingping Zhao , Hua Jin , Abel Lajtha , John M. Davis , Robert C. Smith
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引用次数: 6

Abstract

Some of the biochemical abnormalities underlying schizophrenia, involve differences in methylation and methylating enzymes, as well as other related target genes. We present results of a study of differences in mRNA expression in peripheral blood lymphocytes (PBLs) and post-mortem brains of chronic schizophrenics (CSZ) and non-psychotic controls (NPC), emphasizing the differential effects of sex and antipsychotic drug treatment on mRNA findings. We studied mRNA expression in lymphocytes of 61 CSZ and 49 NPC subjects using qPCR assays with TaqMan probes to assess levels of DNMT, TET, GABAergic, NR3C1, BDNF mRNAs, and several additional targets identified in a recent RNA sequence analysis. In parallel we studied DNMT1 and GAD67 in samples of brain tissues from 19 CSZ, 26 NPC. In PBLs DNMT1 and DNMT3A mRNA levels were significantly higher in male CSZ vs NPC No significant differences were detected in females. The GAD1, NR3C1 and CNTNAP2 mRNA levels were significantly higher in CSZ than NPC. In CSZ patients treated with clozapine, GAD-1 related, CNTNAP2, and IMPA2 mRNAs were significantly higher than in CSZ subjects not treated with clozapine. Differences between CSZ vs NPC in these mRNAs was primarily attributable to the clozapine treatment. In the brain samples, DNMT1 was significantly higher and GAD67 was significantly lower in CSZ than in NPC, but there were no significant sex differences in diagnostic effects. These findings highlight the importance of considering sex and drug treatment effects in assessing the substantive significance of differences in mRNAs between CSZ and NPC.

精神分裂症患者和非精神病性对照组淋巴细胞和大脑甲基化周期及相关基因的基因表达
精神分裂症的一些生化异常包括甲基化和甲基化酶以及其他相关靶基因的差异。我们报告了慢性精神分裂症患者(CSZ)和非精神病对照组(NPC)的外周血淋巴细胞(pbl)和死后大脑mRNA表达差异的研究结果,强调了性别和抗精神病药物治疗对mRNA表达的差异影响。我们研究了61例CSZ和49例NPC受试者的淋巴细胞中mRNA的表达,使用qPCR方法和TaqMan探针来评估DNMT、TET、GABAergic、NR3C1、BDNF mRNA的水平,以及最近在RNA序列分析中发现的一些其他靶标。同时,我们研究了19例CSZ, 26例NPC脑组织样本中的DNMT1和GAD67。在pbl中,DNMT1和DNMT3A mRNA水平在男性CSZ与NPC中显著升高,而在女性中未发现显著差异。CSZ中GAD1、NR3C1和CNTNAP2 mRNA水平显著高于NPC。在接受氯氮平治疗的CSZ患者中,GAD-1相关mrna、CNTNAP2和IMPA2 mrna显著高于未接受氯氮平治疗的CSZ患者。CSZ与NPC在这些mrna上的差异主要归因于氯氮平治疗。脑样本中,CSZ患者DNMT1显著高于NPC患者,GAD67显著低于NPC患者,但在诊断效果上无显著性别差异。这些发现强调了在评估CSZ和NPC之间mrna差异的实质性意义时考虑性别和药物治疗效果的重要性。
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来源期刊
Biomarkers in Neuropsychiatry
Biomarkers in Neuropsychiatry Medicine-Psychiatry and Mental Health
CiteScore
4.00
自引率
0.00%
发文量
12
审稿时长
7 weeks
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