DNA Methylation Pattern of Gene Promoters of MB-COMT, DRD2, and NR3C1 in Turkish Patients Diagnosed with Schizophrenia.

IF 2.4 4区 医学 Q3 NEUROSCIENCES
Hasan Mervan Aytac, Yasemin Oyaci, Mustafa Pehlivan, Sacide Pehlivan
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引用次数: 5

Abstract

Objective: We aim to evaluate the methylation status of membrane-bound catechol-O-methyltransferase (MB-COMT) promotor, dopamine receptor D2 (DRD2), and nuclear receptor subfamily 3 group C member 1 (NR3C1) gene in pa- tients with SCZ by comparing healthy controls.

Methods: A sample of 110 patients with SCZ and 100 age- and sex-matched healthy volunteers was included in the study. The interview was started by filling out data forms that included sociodemographic and clinical information. The Structured Clinical Interview for DSM-IV Axis I Disorders was used to confirming the diagnosis according to DSM-IV-TR criteria. Then the patients were evaluated with the Positive and Negative Symptoms Scale in terms of symp- tom severity. Methylation-specific polymerase chain reaction was used to determine the methylation status of MB-COMT promotor, DRD2 , and NR3C1 gene from DNA material.

Results: When we compared the percentages of MB-COMT promotor, DRD2, and NR3C1 gene methylation status in SCZ patients with the healthy control group, the percentages of MB-COMT promotor (OR: 0.466; 95% CI: 0.268- 0.809; p = 0.006), DRD2 (OR: 0.439; 95% CI: 0.375-0.514; p < 0.001), and NR3C1 (OR: 0.003; 95% CI: 0.001- 0.011; p < 0.001) gene methylation status of SCZ was found to be significantly different from the control group. Whereas unmethylation of MB-COMT promotor and NR3C1 genes were associated with SCZ, the partial methylation of the DRD2 gene was related to the SCZ.

Conclusion: The MB-COMT promotor, DRD2, and NR3C1 gene methylation status may be associated with the SCZ in the Turkish population.

土耳其精神分裂症患者MB-COMT、DRD2和NR3C1基因启动子的DNA甲基化模式
目的:通过与健康对照比较,评估SCZ患者膜结合儿茶酚o -甲基转移酶(MB-COMT)启动子、多巴胺受体D2 (DRD2)和核受体亚家族3组C成员1 (NR3C1)基因的甲基化状况。方法:选取110例SCZ患者和100名年龄、性别匹配的健康志愿者为研究对象。访谈从填写包括社会人口统计和临床信息在内的数据表格开始。根据DSM-IV- tr标准,采用DSM-IV轴I障碍的结构化临床访谈来确认诊断。然后用阳性症状量表和阴性症状量表评定患者的症状严重程度。甲基化特异性聚合酶链反应用于测定DNA材料中MB-COMT启动子、DRD2和NR3C1基因的甲基化状态。结果:当我们将SCZ患者中MB-COMT启动子、DRD2和NR3C1基因甲基化状态的百分比与健康对照组进行比较时,MB-COMT启动子的百分比(OR: 0.466;95% ci: 0.268- 0.809;p = 0.006), DRD2 (OR: 0.439;95% ci: 0.375-0.514;p < 0.001), NR3C1 (OR: 0.003;95% ci: 0.001- 0.011;p < 0.001) SCZ基因甲基化状态与对照组有显著差异。MB-COMT启动子和NR3C1基因的非甲基化与SCZ有关,DRD2基因的部分甲基化与SCZ有关。结论:MB-COMT启动子、DRD2和NR3C1基因甲基化状态可能与土耳其人群的SCZ有关。
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来源期刊
Clinical Psychopharmacology and Neuroscience
Clinical Psychopharmacology and Neuroscience NEUROSCIENCESPHARMACOLOGY & PHARMACY-PHARMACOLOGY & PHARMACY
CiteScore
4.70
自引率
12.50%
发文量
81
期刊介绍: Clinical Psychopharmacology and Neuroscience (Clin Psychopharmacol Neurosci) launched in 2003, is the official journal of The Korean College of Neuropsychopharmacology (KCNP), and the associate journal for Asian College of Neuropsychopharmacology (AsCNP). This journal aims to publish evidence-based, scientifically written articles related to clinical and preclinical studies in the field of psychopharmacology and neuroscience. This journal intends to foster and encourage communications between psychiatrist, neuroscientist and all related experts in Asia as well as worldwide. It is published four times a year at the last day of February, May, August, and November.
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