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催产素能系统基因中的遗传变异及其与产后抑郁易感性的关联。

Genetic Variants in Oxytocinergic System Genes and Their Association with Postpartum Depression Susceptibility.

作者信息

Ciolac Livia, Andreescu Nicoleta Ioana, Farcaș Simona Sorina, Bernad Elena Silvia, Tudor Anca, Nițu Dumitru-Răzvan, Popa Daian-Ionel, Maghiari Anca-Laura, Craina Marius Lucian

机构信息

Doctoral School, Faculty of General Medicine, "Victor Babes" University of Medicine and Pharmacy Timisoara, 300041 Timisoara, Romania.

Department of Microscopic Morphology, Discipline of Genetics, Genomic Medicine Centre, "Victor Babes" University of Medicine and Pharmacy Timisoara, 2 Eftimie Murgu Square, 300041 Timisoara, Romania.

出版信息

Int J Mol Sci. 2025 Feb 27;26(5):2129. doi: 10.3390/ijms26052129.

Abstract

One of the most frequent forms of maternal morbidity following childbirth is postpartum depression. Postpartum depression (PPD), a disabling condition as a major public health concern, has a significant negative impact on the child's emotional, mental as well as intellectual development if left undiagnosed and untreated, which can later have long-term complications. The oxytocin system is an excellent candidate gene system in the maternal context. Differences in vulnerability of mothers for the onset of postpartum psychiatric disorders could be influenced by individual differences in the genetic profile of each one. In this original research, we aimed to explore if there are any possible contributions of genetic variation on both the oxytocin receptor gene (OXTR) and the oxytocin gene (OXT) to the occurrence of postpartum depression, aiming to provide the latest evidence and determine which genetic polymorphisms significantly create a susceptibility for this condition. A total of 100 mothers were preliminarily genotyped before they completed the Edinburgh Postnatal Depression Scale Questionnaire (EPDS) at 6 weeks postpartum. DNA was extracted from peripheral blood samples of the participants (N = 100) and evaluated for the oxytocin gene (OXT_rs2740210; OXT_rs4813627) and oxytocin receptor gene (OXTR_ rs237885) single nucleotide polymorphisms. The results highlighted a significant interaction between the oxytocin OXT_rs2740210 genotype and maternal postpartum depression in mothers with the CC genotype but not in those with AA/AC genotypes. This reveals that an interaction of vulnerable genotypes (CC genotype of OXT_rs2740210, C allele in genotype of OXT_rs2740210, G allele in genotype of OXT_rs4813627) with an environmental burden or other risk factors would predispose the mothers to develop postpartum depression. We found no significant association between the interaction effect of the oxytocin receptor gene OXTR_rs237885 genotype depending on the occurrence of maternal postpartum depression. These findings prove the implication of the oxytocinergic system gene variants in vulnerability for postpartum depression and indicate the need for future studies adopting a multilevel approach in order to increase understanding.

摘要

产后抑郁症是分娩后最常见的产妇发病形式之一。产后抑郁症(PPD)是一种致残性疾病,是一个主要的公共卫生问题,如果不进行诊断和治疗,会对儿童的情感、心理和智力发展产生重大负面影响,随后可能会引发长期并发症。在产妇的情况下,催产素系统是一个优秀的候选基因系统。母亲患产后精神疾病的易感性差异可能受每个人基因特征个体差异的影响。在这项原创研究中,我们旨在探讨催产素受体基因(OXTR)和催产素基因(OXT)的基因变异对产后抑郁症的发生是否有任何可能的影响,旨在提供最新证据并确定哪些基因多态性会显著增加患这种疾病的易感性。共有100名母亲在产后6周完成爱丁堡产后抑郁量表问卷(EPDS)之前进行了初步基因分型。从参与者(N = 100)的外周血样本中提取DNA,并评估催产素基因(OXT_rs2740210;OXT_rs4813627)和催产素受体基因(OXTR_ rs237885)的单核苷酸多态性。结果突出显示,在CC基因型的母亲中,催产素OXT_rs2740210基因型与产妇产后抑郁症之间存在显著相互作用,而在AA/AC基因型的母亲中则不存在这种相互作用。这表明,脆弱基因型(OXT_rs2740210的CC基因型、OXT_rs2740210基因型中的C等位基因、OXT_rs4813627基因型中的G等位基因)与环境负担或其他风险因素之间的相互作用会使母亲易患产后抑郁症。我们发现,催产素受体基因OXTR_rs237885基因型的相互作用效应与产妇产后抑郁症的发生之间没有显著关联。这些发现证明了催产素能系统基因变异在产后抑郁症易感性中的作用,并表明未来需要采用多层次方法进行研究,以增进理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/678c/11899787/9275cf2fcbc6/ijms-26-02129-g001.jpg

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