Department of Molecular Biology and Cell Pathology, Third Faculty of Medicine, Charles University, 100 00 Prague, Czech Republic.
Institute for the Care of the Mother and Child, Third Faculty of Medicine, Charles University, 147 00 Prague, Czech Republic.
Int J Mol Sci. 2020 Nov 9;21(21):8413. doi: 10.3390/ijms21218413.
The goal was to assess how a history of any kind of pregnancy-related complication altered expression profile of microRNAs played a role in the pathogenesis of diabetes, cardiovascular and cerebrovascular diseases in the peripheral blood leukocytes of children at the age of 3-11 years. The prior exposure to gestational hypertension, preeclampsia, fetal growth restriction, gestational diabetes mellitus, preterm prelabor rupture of membranes or spontaneous preterm birth causes that a significant proportion of children (57.42% to 90.0% specifically) had a substantially altered microRNA expression profile, which might be the origin of a lifelong cardiovascular risk. A total of 23 out of 29 tested microRNAs were upregulated in children born from such complicated gestation. The occurrence of overweight, obesity, valve problems and heart defects even intensified upregulation of microRNAs already present in children exposed to such pregnancy complications. The occurrence of overweight/obesity (miR-92a-3p, and miR-210-3p) and valve problems or heart defects (miR-342-3p) induced microRNA upregulation in children affected with pregnancy complications. Overall, 42.86% overweight/obese children and 27.36% children with valve problems or heart defects had even higher microRNA levels than children with normal clinical findings after complicated pregnancies. In addition, the microRNA expression profile was also able to differentiate between children descending from normal gestation in relation to the occurrence of overweight and obesity. Screening on the base of the combination of 19 microRNAs identified 70.0% overweight/obese children at 90.0% specificity. In general, children after complicated pregnancies, just as children after normal pregnancies, with abnormal findings are at a higher risk of the onset of cardiovascular complications, and their dispensarization, with the aim to implement primary prevention strategies, would be beneficial.
目的在于评估任何一种与妊娠相关的并发症史如何改变微 RNA 的表达谱,从而在 3-11 岁儿童的外周血白细胞中发挥作用,导致糖尿病、心血管和脑血管疾病的发病机制。先前暴露于妊娠高血压、子痫前期、胎儿生长受限、妊娠糖尿病、胎膜早破或自发性早产会导致相当一部分儿童(具体为 57.42%至 90.0%)的微 RNA 表达谱发生显著改变,这可能是终生心血管风险的根源。在这些复杂妊娠中出生的儿童中,有 23 种微 RNA 被检测到上调。超重、肥胖、瓣膜问题和心脏缺陷的发生甚至加剧了暴露于这些妊娠并发症的儿童中已经存在的微 RNA 的上调。超重/肥胖(miR-92a-3p 和 miR-210-3p)和瓣膜问题或心脏缺陷(miR-342-3p)的发生诱导了受妊娠并发症影响的儿童的微 RNA 上调。总体而言,42.86%的超重/肥胖儿童和 27.36%的瓣膜问题或心脏缺陷儿童的微 RNA 水平甚至高于正常临床发现的复杂妊娠后儿童。此外,微 RNA 表达谱还能够区分正常妊娠和超重/肥胖儿童。基于 19 种微 RNA 的组合进行筛查,可在 90.0%的特异性下识别出 70.0%的超重/肥胖儿童。一般来说,复杂妊娠后的儿童,就像正常妊娠后的儿童一样,有异常发现的儿童发生心血管并发症的风险更高,对他们进行分诊,以实施初级预防策略,将是有益的。