Tozzi Maria Giulia, Moscuzza Francesca, Michelucci Angela, Lorenzoni Francesca, Cosini Cinzia, Ciantelli Massimiliano, Ghirri Paolo
Division of Neonatology and NICU, Department of Clinical and Experimental Medicine, Pisa, Italy.
Molecular Genetics Lab, University Hospital of Pisa, Pisa, Italy.
Front Pediatr. 2018 Dec 20;6:408. doi: 10.3389/fped.2018.00408. eCollection 2018.
IntraUterine (IUGR) and ExtraUterine Growth Restriction (EUGR) may induce reprogramming mechanisms, finalized to survive before and after birth. Nutritional factors and other environmental signals could regulate gene expression through epigenetic modification, but the molecular mechanisms involved are not yet well understood. Epigenetic mechanisms could be considered as a bridge between environmental stimuli and long lasting phenotype, acquired during the intrauterine life and the first weeks of life. Our aim was to investigate the relationship between growth patterns, nutritional determinants, and epigenetic pathways. We enrolled 38 newborns admitted to Neonatal Intensive Care Unit (NICU) at University Hospital of Pisa. Gestational age at birth was <34 weeks and post-menstrual age (PMA) was 36-42 weeks at discharge. We excluded infants with malformations or clinical syndromes. EUGR was defined as the reduction in weight z score between birth and discharge >1 SD. We also evaluated DNA methylation of Imprinting Centre 1 (IC1) at birth and at discharge. We observed a decrease in SD of weight and head circumference mainly during the first weeks of life. We found a correlation between EUGR for weight and for head circumference and an increased IC1 methylation ( = 0.018 and = 0.0028, respectively). We observed a relationship between reduced protein and lipid intake and IC1 hypermethylation ( = 0.009 and = 0.043, respectively). IC1 hypermethylation could be a reprogramming mechanism to promote a catch-up growth, by means of an increased Insulin-like growth factor 2 (IGF2) expression, that may have potential effects on metabolic homeostasis later in life.
宫内生长受限(IUGR)和宫外生长受限(EUGR)可能会引发重编程机制,其目的是在出生前后存活下来。营养因素和其他环境信号可通过表观遗传修饰来调节基因表达,但其中涉及的分子机制尚未完全明确。表观遗传机制可被视为环境刺激与持久表型之间的桥梁,这种表型是在子宫内生活和出生后的头几周获得的。我们的目的是研究生长模式、营养决定因素与表观遗传途径之间的关系。我们纳入了38名入住比萨大学医院新生儿重症监护病房(NICU)的新生儿。出生时的胎龄小于34周,出院时的孕龄(PMA)为36 - 42周。我们排除了有畸形或临床综合征的婴儿。EUGR被定义为出生至出院期间体重z评分降低超过1个标准差。我们还评估了出生时和出院时印记中心1(IC1)的DNA甲基化情况。我们观察到体重和头围的标准差主要在出生后的头几周有所下降。我们发现体重和头围的EUGR与IC1甲基化增加之间存在相关性(分别为 = 0.018和 = 0.0028)。我们观察到蛋白质和脂质摄入量减少与IC1高甲基化之间存在关系(分别为 = 0.009和 = 0.043)。IC1高甲基化可能是一种重编程机制,通过增加胰岛素样生长因子2(IGF2)的表达来促进追赶生长,这可能会对日后的代谢稳态产生潜在影响。