Institute of Graduate Studies in Health Sciences, Istanbul University, Istanbul, Turkey.
Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Turkey.
J Investig Med. 2024 Jun;72(5):449-456. doi: 10.1177/10815589241242715. Epub 2024 Apr 25.
We aim to investigate the methylation of gene promotor and polymorphism in schizophrenia (SCZ) patients with attempted suicide or non-suicidal self-injury (NSSI). A sample of 112 patients with SCZ was included in the study. Structured Clinical Interview for Diagnostic and Statistical Manual-Fourth Edition Axis I Disorders was used to confirm the diagnosis according to The Diagnostic and Statistical Manual of Mental Disorders, fourth edition, text revision criteria. The patients were evaluated by data forms that had sociodemographic, suicidal behavior, and NSSI information. Methylation-specific polymerase chain reaction (PCR) was used to identify the methylation of the gene. The analysis of the BclI polymorphism of the gene was evaluated by using the PCR restriction fragment length polymorphism. Our results revealed that although the NR3C1 gene methylation was not statistically significantly different, there was a significant difference in NR3C1 genotype distribution among the SCZ groups with and without attempted suicide. SCZ patients carrying the CC genotype had a lower risk of attempted suicide (Odds Ratio [OR]: 0.421; 95% Confidence Interval [CI]: 0.183-0.970; p = 0.040), while having the GG genotype in SCZ patients was associated with a higher risk of attempted suicide (OR: 3.785; 95% Cl: 1.107-12.945; p = 0.042). Additionally, due to NSSI in SCZ patients, there were no significant differences in NR3C1 gene methylation and genotype distribution among the groups. We propose that the BclI polymorphism may be associated with attempted suicide in Turkish patients diagnosed with SCZ.
我们旨在探讨自杀未遂或非自杀性自伤(NSSI)精神分裂症(SCZ)患者基因启动子甲基化和多态性。研究纳入了 112 例 SCZ 患者。采用《精神障碍诊断与统计手册》第四版轴 I 障碍的结构临床访谈对诊断进行确认。根据《精神障碍诊断与统计手册》第四版修订本的标准,对患者进行了包括社会人口统计学、自杀行为和 NSSI 信息在内的数据表评估。采用甲基化特异性聚合酶链反应(PCR)鉴定基因的甲基化。采用聚合酶链反应限制性片段长度多态性分析方法评估基因的 BclI 多态性。我们的结果表明,尽管 NR3C1 基因甲基化无统计学显著差异,但在有自杀未遂和无自杀未遂的 SCZ 组之间,NR3C1 基因型分布存在显著差异。携带 CC 基因型的 SCZ 患者自杀未遂的风险较低(优势比 [OR]:0.421;95%置信区间 [CI]:0.183-0.970;p=0.040),而 SCZ 患者携带 GG 基因型与自杀未遂的风险较高相关(OR:3.785;95% Cl:1.107-12.945;p=0.042)。此外,由于 SCZ 患者存在 NSSI,NR3C1 基因甲基化和基因型分布在各组之间无显著差异。我们提出,BclI 多态性可能与土耳其诊断为 SCZ 的患者自杀未遂有关。