Hromadnikova Ilona, Kotlabova Katerina, Krofta Ladislav
Department of Molecular Biology and Cell Pathology, Third Faculty of Medicine, Charles University, 110 00 Prague, Czech Republic.
Institute for the Care of the Mother and Child, Third Faculty of Medicine, Charles University, 147 00 Prague, Czech Republic.
J Pers Med. 2021 Jan 11;11(1):39. doi: 10.3390/jpm11010039.
The principal goal of the study was to map common postpartal alterations in gene expression of microRNAs associated with diabetes/cardiovascular/cerebrovascular diseases induced by most frequently occurring pregnancy-related complications (gestational hypertension, preeclampsia, fetal growth restriction, gestational diabetes mellitus, preterm prelabor rupture of membranes, or spontaneous preterm birth). In addition, the association analyses between individual abnormal clinical findings (overweight/obesity, central obesity, hypertension, on blood pressure treatment, history of infertility treatment, actual hormonal contraceptive use, the presence of trombophilic gene mutations, actual smoking status, increased serum levels of total cholesterol, HDL (high density lipoprotein) cholesterol, LDL (low density lipoprotein) cholesterol, triglycerides, lipoprotein A, CRP (C-reactive protein), and uric acid, and increased plasma levels of homocysteine) and microRNA expression levels were performed in mothers with respect/regardless to previous course of gestation. The prior exposure to gestational hypertension, preeclampsia, fetal growth restriction, gestational diabetes mellitus, preterm prelabor rupture of membranes, or spontaneous preterm birth caused that a significant proportion of mothers (52.42% at 90.0% specificity) had substantially altered microRNA expression profile, which might originate lifelong cardiovascular risk. 26 out of 29 tested microRNAs were up-regulated in mothers with a history of such complicated pregnancies. MicroRNA expression profiles were also able to differentiate between mothers with normal and abnormal clinical findings (BMI (body mass index), waist circumference, systolic blood pressure, on blood pressure treatment, history of infertility treatment, and the presence of trombophilic gene mutations) irrespective of previous course of gestation. The treatment of hypertension even intensified upregulation of some microRNAs (miR-24-3p, and miR-342-3p) already present in women after complicated pregnancies. Newly, the presence of overweight/obesity (miR-155-5p), systolic hypertension (miR-92a-3p, and miR-210-3p), treatment for infertility (miR-155-5p), and treatment for hypertension (miR-210-3p) induced upregulation of several microRNAs. In general, mothers after complicated pregnancies are at increased risk of development of cardiovascular complications. Especially those mothers indicated to have postpartally altered microRNA expression profiles might be considered as a highly risky group that would benefit from dispensarization and implementation of primary prevention strategies.
该研究的主要目标是描绘与最常见的妊娠相关并发症(妊娠期高血压、先兆子痫、胎儿生长受限、妊娠期糖尿病、胎膜早破或自然早产)所引发的糖尿病/心血管疾病/脑血管疾病相关的微小RNA基因表达的常见产后变化。此外,针对有/无既往妊娠史的母亲,对个体异常临床发现(超重/肥胖、中心性肥胖、高血压、正在接受血压治疗、不孕治疗史、当前使用激素避孕药、存在血栓形成倾向基因突变、当前吸烟状况、血清总胆固醇、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇、甘油三酯、脂蛋白A、C反应蛋白和尿酸水平升高,以及血浆同型半胱氨酸水平升高)与微小RNA表达水平之间进行了关联分析。既往暴露于妊娠期高血压、先兆子痫、胎儿生长受限、妊娠期糖尿病、胎膜早破或自然早产导致相当比例的母亲(在特异性为90.0%时为52.42%)的微小RNA表达谱发生了显著改变,这可能会引发终身心血管风险。在有此类复杂妊娠史的母亲中,29个检测的微小RNA中有26个上调。无论既往妊娠史如何,微小RNA表达谱也能够区分有正常和异常临床发现(体重指数、腰围、收缩压、正在接受血压治疗、不孕治疗史以及存在血栓形成倾向基因突变)的母亲。高血压治疗甚至会加剧复杂妊娠后女性体内已存在的一些微小RNA(miR - 24 - 3p和miR - 342 - 3p)的上调。最近,超重/肥胖(miR - 155 - 5p)、收缩期高血压(miR - 92a - 3p和miR - 210 - 3p)、不孕治疗(miR - 155 - 5p)和高血压治疗(miR - 210 - 3p)会诱导几种微小RNA上调。总体而言,经历复杂妊娠后的母亲发生心血管并发症的风险增加。特别是那些产后微小RNA表达谱显示有改变的母亲可能被视为高风险群体,她们将从疾病防治和一级预防策略的实施中受益。