• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[In utero fetal programming and its impact on health in adulthood].

作者信息

Ramírez-Vélez Robinson

机构信息

Programa de Medicina, Ciencias Básicas, Fisiología, Universidad ICESI, Santiago de Cali, Valle del Cauca, Colombia.

出版信息

Endocrinol Nutr. 2012 Jun-Jul;59(6):383-93. doi: 10.1016/j.endonu.2012.02.002. Epub 2012 Apr 6.

DOI:10.1016/j.endonu.2012.02.002
PMID:22483564
Abstract

Adverse events during intrauterine life may program organ growth and favor disease later in life. This is the usually called 'Barker's hypothesis'. Increasing evidence suggests that conditions like vascular disease, hypertension, metabolic syndrome, and type 2 diabetes mellitus are programmed during the early stages of fetal development and become manifest in late stages of life, when there is an added impact of lifestyle and other conventional acquired environmental risk factors that interact with genetic factors. The aim of this review was to provide additional, updated evidence to support the association between intrauterine fetal health and increased prevalence of chronic non-communicable diseases in adulthood. Various potential cellular and molecular mechanisms proposed to be related to the above hypothesis are discussed, including endothelial function, oxidative stress, insulin resistance, and mitochondrial function.

摘要

相似文献

1
[In utero fetal programming and its impact on health in adulthood].
Endocrinol Nutr. 2012 Jun-Jul;59(6):383-93. doi: 10.1016/j.endonu.2012.02.002. Epub 2012 Apr 6.
2
In utero origins of adult insulin resistance and vascular dysfunction.胎儿期胰岛素抵抗和血管功能障碍的起源。
Semin Reprod Med. 2011 May;29(3):211-24. doi: 10.1055/s-0031-1275522. Epub 2011 Jun 27.
3
Fetal programming of atherosclerosis: possible role of the mitochondria.胎儿期动脉粥样硬化的形成:线粒体的可能作用。
Eur J Obstet Gynecol Reprod Biol. 2010 Apr;149(2):127-30. doi: 10.1016/j.ejogrb.2009.12.005. Epub 2010 Jan 6.
4
[Foetal programming of nutrition-related chronic diseases].[营养相关慢性疾病的胎儿编程]
Sante. 2002 Jan-Mar;12(1):56-63.
5
[Fetal programming--the intrauterine origin of adult morbidity].[胎儿编程——成人疾病的宫内起源]
Harefuah. 2005 Feb;144(2):97-101, 151, 150.
6
Tracing the origins of "fetal origins" of adult diseases: programming by oxidative stress?探寻成人疾病“胎儿起源”的根源:氧化应激编程?
Med Hypotheses. 2006;66(1):38-44. doi: 10.1016/j.mehy.2005.08.020. Epub 2005 Sep 27.
7
[Fetal weight at weight as predisposing risk factor for type 2 diabetes in adulthood].[胎儿体重作为成年期2型糖尿病的易感风险因素]
Ginecol Obstet Mex. 2001 Oct;69:390-8.
8
Fetal and neonatal programming: evidence and clinical implications.胎儿及新生儿编程:证据与临床意义
Am J Perinatol. 2009 Mar;26(3):191-8. doi: 10.1055/s-0028-1103027. Epub 2008 Nov 21.
9
The fetal origin of adult diseases.成人疾病的胎儿起源。
J Obstet Gynaecol. 2003 Sep;23(5):555-60. doi: 10.1080/0144361031000156483.
10
[Nephropathy associated with arterial hypertension: genes and Barker's hypothesis].[与动脉高血压相关的肾病:基因与巴克假说]
G Ital Nefrol. 2002 Sep-Oct;19(5):517-22.

引用本文的文献

1
A dataset of synthetic, maturation-informed magnetic resonance images of the human fetal brain.一个包含人类胎儿大脑合成的、成熟度相关磁共振图像的数据集。
Sci Data. 2025 Apr 10;12(1):602. doi: 10.1038/s41597-025-04926-9.
2
Rapid Growth between 0 and 2 Years Old in Healthy Infants Born at Term and Its Relationship with Later Obesity: A Systematic Review and Meta-Analysis of Evidence.健康足月出生婴儿在 0 至 2 岁期间的快速生长及其与后期肥胖的关系:系统评价和证据的荟萃分析。
Nutrients. 2024 Sep 2;16(17):2939. doi: 10.3390/nu16172939.
3
Preconceptional maternal hyperandrogenism and metabolic syndrome risk in male offspring: a long-term population-based study.
孕前母体高雄激素血症与男性子代代谢综合征风险:一项基于人群的长期研究。
J Endocrinol Invest. 2024 Nov;47(11):2731-2743. doi: 10.1007/s40618-024-02374-7. Epub 2024 Apr 22.
4
Molecular Indicators of Blood-Brain Barrier Breakdown and Neuronal Injury in Pregnancy Complicated by Fetal Growth Restriction.胎儿生长受限合并妊娠时血脑屏障破坏和神经元损伤的分子指标
Int J Mol Sci. 2022 Nov 9;23(22):13798. doi: 10.3390/ijms232213798.
5
Effect of Exercise on the Resting Metabolic Rate and Substrate Utilization in Women with Gestational Diabetes Mellitus: Results of a Pilot Study.运动对妊娠期糖尿病女性静息代谢率和底物利用的影响:一项初步研究的结果。
Metabolites. 2022 Oct 20;12(10):998. doi: 10.3390/metabo12100998.
6
Foetal lipoprotein oxidation and preeclampsia.胎儿脂蛋白氧化与子痫前期。
Lipids Health Dis. 2022 Jun 4;21(1):51. doi: 10.1186/s12944-022-01663-5.
7
A Fetal Brain magnetic resonance Acquisition Numerical phantom (FaBiAN).胎儿脑磁共振采集数值体模(FaBiAN)。
Sci Rep. 2022 May 23;12(1):8682. doi: 10.1038/s41598-022-10335-4.
8
Maternal Oxidative Stress Biomarkers in Pregnancy and Child Growth from Birth to Age 6.孕期母体氧化应激生物标志物与儿童生长:从出生到 6 岁。
J Clin Endocrinol Metab. 2021 Apr 23;106(5):1427-1436. doi: 10.1210/clinem/dgab018.
9
Use of dietary supplements by pregnant women in Colombia.哥伦比亚孕妇对膳食补充剂的使用情况。
BMC Pregnancy Childbirth. 2018 May 2;18(1):117. doi: 10.1186/s12884-018-1758-5.
10
Neonatal Lipopolysaccharide Exposure Gender-Dependently Increases Heart Susceptibility to Ischemia/Reperfusion Injury in Male Rats.新生大鼠脂多糖暴露致雄性大鼠心脏对缺血/再灌注损伤的易感性增加具有性别依赖性。
Int J Med Sci. 2017 Sep 19;14(11):1163-1172. doi: 10.7150/ijms.20285. eCollection 2017.