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土耳其精神分裂症患者中MB - COMT、DRD2和NR3C1基因启动子的DNA甲基化模式

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

作者信息

Aytac Hasan Mervan, Oyaci Yasemin, Pehlivan Mustafa, Pehlivan Sacide

机构信息

Department of Psychiatry, Basaksehir Cam and Sakura City Hospital, Istanbul, Turkey.

Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.

出版信息

Clin Psychopharmacol Neurosci. 2022 Nov 30;20(4):685-693. doi: 10.9758/cpn.2022.20.4.685. Epub 2021 Jun 14.

Abstract

OBJECTIVE

We aim to evaluate the methylation status of membrane-bound catechol-O-methyltransferase () promotor, dopamine receptor D2 (), and nuclear receptor subfamily 3 group C member 1 () 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 promotor, , and gene from DNA material.

RESULTS

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

CONCLUSION

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

摘要

目的

通过与健康对照进行比较,评估精神分裂症(SCZ)患者中膜结合儿茶酚 - O - 甲基转移酶()启动子、多巴胺受体D2()和核受体亚家族3组C成员1()基因的甲基化状态。

方法

本研究纳入了110例SCZ患者和100名年龄及性别匹配的健康志愿者。通过填写包含社会人口统计学和临床信息的数据表开始访谈。使用《精神障碍诊断与统计手册》第四版轴I障碍的结构化临床访谈,根据DSM - IV - TR标准确诊。然后使用阳性和阴性症状量表评估患者的症状严重程度。采用甲基化特异性聚合酶链反应从DNA材料中确定启动子、和基因的甲基化状态。

结果

当我们将SCZ患者中启动子、和基因甲基化状态的百分比与健康对照组进行比较时,发现SCZ患者启动子(OR:0.466;95% CI:0.268 - 0.809; = 0.006)、(OR:0.439;95% CI:0.375 - 0.514; < 0.001)和(OR:0.003;95% CI:0.001 - 0.011; < 0.001)基因的甲基化状态与对照组有显著差异。启动子和基因的未甲基化与SCZ相关,而基因的部分甲基化与SCZ有关。

结论

在土耳其人群中,MB - COMT启动子、和基因的甲基化状态可能与SCZ有关。

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