Penezić Ana, Radojičić Ognjen, Stevanović Jovana, Robajac Dragana, Miljuš Goran, Šunderić Miloš, Ardalić Daniela, Mandić-Marković Vesna, Miković Željko, Nedić Olgica, Dobrijević Zorana
University of Belgrade- Institute for the Application of Nuclear Energy, Belgrade, Serbia.
University Clinic for Gynecology and Obstetrics "Narodni Front", Belgrade, Serbia.
Mol Biol Rep. 2025 Jul 1;52(1):661. doi: 10.1007/s11033-025-10778-8.
Gestational diabetes (GDM) is the most common pregnancy-related metabolic disorder and a major risk factor for both mother and a child, during pregnancy and after delivery. Impairment of the anti-oxidative system acts as the driving force of the devastating consequences in GDM, while microRNA molecules are affected by disturbances related to (glyco)oxidative stress ((g)OS) and emerged as potential sensors and effectors of (g)OS-associated mechanisms.
The aim of the present study was to evaluate the potential of OS-related microRNAs miR-27a, miR-222 and miR-340 from peripheral blood mononuclear cells (PBMCs) to serve as OS indicators of in GDM.
MicroRNA quantification was conducted in samples of patients with GDM and normoglycemic controls (n = 45 each). Levels of expression were tested for correlations with the activities of glutathione reductase (GR), superoxide dismutase (SOD) and catalase (CAT) and serum thiol content. MiR-27a demonstrated correlation with the expression of other two microRNAs. GR activity during pregnancy weeks 24-28 was increased in GDM, while thiol content showed an opposite direction of change. Similar results were acquired when comparing GDM patients with and without adverse pregnancy outcomes. The expression of tested microRNAs was positively correlated with the activity of GR in GDM group, while the correlation of the expression of miR-27a-3p and miR-340-5p with SOD activity and blood thiol content was negative.
Our findings support the relevance of redox dysregulation in mid-pregnancy for developing obstetric and neonatal complications. The results also qualify miR-27a-3p, miR-222-3p and miR-340-5p for redox status indicators in GDM.
妊娠期糖尿病(GDM)是最常见的妊娠相关代谢紊乱疾病,是孕期及产后母婴的主要危险因素。抗氧化系统受损是妊娠期糖尿病产生严重后果的驱动因素,而微小RNA分子受(糖)氧化应激((g)OS)相关干扰的影响,并成为(g)OS相关机制的潜在传感器和效应器。
本研究旨在评估外周血单核细胞(PBMCs)中与氧化应激相关的微小RNA miR-27a、miR-222和miR-340作为妊娠期糖尿病氧化应激指标的潜力。
对妊娠期糖尿病患者和血糖正常对照组的样本(每组n = 45)进行微小RNA定量分析。检测表达水平与谷胱甘肽还原酶(GR)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性以及血清硫醇含量的相关性。MiR-27a与其他两种微小RNA的表达呈相关性。妊娠期糖尿病患者在孕24 - 28周时GR活性升高,而硫醇含量变化方向相反。比较有和没有不良妊娠结局的妊娠期糖尿病患者时也得到了类似结果。在妊娠期糖尿病组中,所检测的微小RNA的表达与GR活性呈正相关,而miR-27a-3p和miR-340-5p的表达与SOD活性和血硫醇含量呈负相关。
我们的研究结果支持妊娠中期氧化还原失调与产科和新生儿并发症发生发展的相关性。结果还表明miR-27a-3p、miR-222-3p和miR-340-5p可作为妊娠期糖尿病氧化还原状态指标。