Developmental programming of cardiovascular disease by prenatal hypoxia

被引:149
作者
Giussani, D. A. [1 ]
Davidge, S. T. [2 ,3 ]
机构
[1] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3EG, England
[2] Univ Alberta, Women & Childrens Hlth Res Inst, Dept Obstet & Gynecol, Edmonton, AB, Canada
[3] Univ Alberta, Women & Childrens Hlth Res Inst, Dept Physiol, Edmonton, AB, Canada
基金
英国生物技术与生命科学研究理事会; 加拿大健康研究院;
关键词
cardiovascular dysfunction; fetal hypoxia; interventions; metabolic syndrome; treatment; INTRAUTERINE GROWTH RESTRICTION; PKC-EPSILON GENE; CHRONIC MODERATE HYPOXIA; INTIMA-MEDIA THICKNESS; HIGH-ALTITUDE HYPOXIA; LOW-BIRTH-WEIGHT; HIGH-FAT DIET; LONG-TERM; FETAL-GROWTH; ADULT MALE;
D O I
10.1017/S204017441300010X
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
It is now recognized that the quality of the fetal environment during early development is important in programming cardiovascular health and disease in later life. Fetal hypoxia is one of the most common consequences of complicated pregnancies worldwide. However, in contrast to the extensive research effort on pregnancy affected by maternal nutrition or maternal stress, the contribution of pregnancy affected by fetal chronic hypoxia to developmental programming is only recently becoming delineated and established. This review discusses the increasing body of evidence supporting the programming of cardiac susceptibility to ischaemia and reperfusion (I/R) injury, of endothelial dysfunction in peripheral resistance circulations, and of indices of the metabolic syndrome in adult offspring of hypoxic pregnancy. An additional focus of the review is the identification of plausible mechanisms and the implementation of maternal and early life interventions to protect against adverse programming.
引用
收藏
页码:328 / 337
页数:10
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