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Fetal programming and diseases in adulthood: A critical analysis

机译:胎儿编程与成年期疾病:一项关键分析

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Fetal malnutrition is an important risk factor for the occurrence of metabolic syndrome in adulthood (cardiovascular disease, high blood pressure, insulin resistance, hyper-lipemia). This concept of metabolic programming is now well established in biology, whereby a stimulus or an insult during a critical or sensitive period of development can have long-term or life-time effects on the organism. The glucose-insulin-IGF system, main regulatory parameter of fetal growth, plays very likely an important role in metabolic programming. Nutritional epi-genomics is another fascinating area of research. As opposed to mutations in the DNA sequence, epigenetic modifications are instable and reversible. They can be influenced by the nutritional status, as shown in animal models and more recently in humans. In infants presenting at birth with severe intrauterine growth retardation (IUGR) due to fetal malnutrition, rapid catch up growth can have an additional deleterious metabolic effect, which is difficult to differentiate from the specific metabolic effects of IUGR.
机译:胎儿营养不良是成年后代谢综合征(心血管疾病,高血压,胰岛素抵抗,高脂血症)发生的重要危险因素。如今,代谢程序设计的这一概念已在生物学中得到了很好的确立,因此,在发育的关键或敏感时期进行刺激或侮辱可能会对生物产生长期或终身影响。葡萄糖-胰岛素-IGF系统是胎儿生长的主要调节参数,很可能在代谢程序中起重要作用。营养表观基因组学是另一个有趣的研究领域。与DNA序列中的突变相反,表观遗传修饰是不稳定和可逆的。它们可能会受到营养状况的影响,如动物模型以及最近在人类中所显示的。在出生时因胎儿营养不良而导致严重的宫内发育迟缓(IUGR)的婴儿中,快速的追赶生长会产生额外的有害代谢作用,这很难与IUGR的特定代谢作用区分开。

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