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非酒精性脂肪性肝病的发育编程:早期营养对晚年易感性和疾病严重程度的影响。

Developmental Programming of Nonalcoholic Fatty Liver Disease: The Effect of Early Life Nutrition on Susceptibility and Disease Severity in Later Life.

作者信息

Li Minglan, Reynolds Clare M, Segovia Stephanie A, Gray Clint, Vickers Mark H

机构信息

Liggins Institute and Gravida: National Centre for Growth and Development, University of Auckland, Auckland 1142, New Zealand.

出版信息

Biomed Res Int. 2015;2015:437107. doi: 10.1155/2015/437107. Epub 2015 May 18.

DOI:10.1155/2015/437107
PMID:26090409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4450221/
Abstract

Nonalcoholic fatty liver disease (NAFLD) is fast becoming the most common liver disease globally and parallels rising obesity rates. The developmental origins of health and disease hypothesis have linked alterations in the early life environment to an increased risk of metabolic disorders in later life. Altered early life nutrition, in addition to increasing risk for the development of obesity, type 2 diabetes, and cardiovascular disease in offspring, is now associated with an increased risk for the development of NAFLD. This review summarizes emerging research on the developmental programming of NAFLD by both maternal obesity and undernutrition with a particular focus on the possible mechanisms underlying the development of hepatic dysfunction and potential strategies for intervention.

摘要

非酒精性脂肪性肝病(NAFLD)正迅速成为全球最常见的肝脏疾病,且与肥胖率上升同步。健康与疾病的发育起源假说将生命早期环境的改变与晚年代谢紊乱风险增加联系起来。生命早期营养改变,除了增加后代患肥胖症、2型糖尿病和心血管疾病的风险外,现在还与患NAFLD风险增加有关。本综述总结了关于母体肥胖和营养不良对NAFLD进行发育编程的新研究,特别关注肝功能障碍发展的潜在机制以及潜在的干预策略。

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本文引用的文献

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Oxidative stress and altered lipid homeostasis in the programming of offspring fatty liver by maternal obesity.母源性肥胖对子代脂肪肝发生的氧化应激与脂质代谢失衡的程序化作用。
Am J Physiol Regul Integr Comp Physiol. 2014 Jul 1;307(1):R26-34. doi: 10.1152/ajpregu.00049.2014. Epub 2014 Apr 30.
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Early life exposure to maternal insulin resistance has persistent effects on hepatic NAFLD in juvenile nonhuman primates.生命早期暴露于母体胰岛素抵抗可对幼年非人类灵长类动物的肝脏 NAFLD 产生持续影响。
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The regulation of hepatic Pon1 by a maternal high-fat diet is gender specific and may occur through promoter histone modifications in neonatal rats.
4岁以下儿童肝脏脂肪变性超声偶然发现的患病率。
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Factors early in life associated with hepatic steatosis.生命早期与肝脂肪变性相关的因素。
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Diets Partially Replaced With Cassava Residue Modulate Antioxidant Capacity, Lipid Metabolism, and Gut Barrier Function of Huanjiang Mini-Pigs.用木薯残渣部分替代的日粮调节环江小型猪的抗氧化能力、脂质代谢和肠道屏障功能。
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Early-Life Exposure to Famine and Risk of Metabolic Associated Fatty Liver Disease in Chinese Adults.早期生活经历饥荒与中国成年人代谢相关脂肪性肝病风险的关系。
Nutrients. 2021 Nov 13;13(11):4063. doi: 10.3390/nu13114063.
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Gestational exposure to high fat diets and bisphenol A alters metabolic outcomes in dams and offspring, but produces hepatic steatosis only in dams.妊娠期间暴露于高脂肪饮食和双酚 A 会改变母鼠及其后代的代谢结果,但仅在母鼠中会引起肝脂肪变性。
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母体高脂饮食对肝脏Pon1的调节具有性别特异性,且可能通过新生大鼠启动子组蛋白修饰发生。
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Accelerated infant weight gain and risk for nonalcoholic fatty liver disease in early adulthood.加速婴儿体重增加与成年早期非酒精性脂肪肝风险。
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