A conceptual framework for the developmental origins of health and disease

被引:309
作者
Gluckman, P. D. [1 ,2 ,3 ]
Hanson, M. A. [4 ]
Buklijas, T. [1 ,2 ]
机构
[1] Univ Auckland, Liggins Inst, Auckland 1023, New Zealand
[2] Univ Auckland, Natl Res Ctr Growth & Dev, Auckland 1023, New Zealand
[3] ASTAR, Singapore Inst Clin Sci, Singapore, Singapore
[4] Univ Southampton, Dev Origins Hlth & Dis Div, Inst Dev Sci, Southampton, Hants, England
关键词
developmental origins of health and disease; life history; plasticity; INTRAUTERINE GROWTH-RETARDATION; CORONARY-HEART-DISEASE; NATIONAL BIRTH COHORT; BODY-MASS INDEX; HIGH-FAT DIET; BLOOD-PRESSURE; DIABETES-MELLITUS; DNA METHYLATION; MATERNAL DIET; FETAL ORIGINS;
D O I
10.1017/S2040174409990171
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In the last decades, the developmental origins of health and disease (DOHaD) have emerged as a vigorous field combining experimental, clinical, epidemiological and public health research. Its goal is to understand how events in early life shape later morbidity risk, especially of non-communicable chronic diseases. As these diseases become the major cause of morbidity and mortality worldwide, research arising from DOHaD is likely to gain significance to public health and economic development. But action may be hindered by the lack of a firm mechanistic explanation and of a conceptual basis, especially regarding the evolutionary significance of the DOHaD phenomenon. In this article, we provide a succinct historical review of the research into the relationship between development and later disease, consider the evolutionary and developmental significance and discuss the underlying mechanisms of the DOHaD phenomenon. DOHaD should be viewed as a part of a broader biological mechanism of plasticity by which organisms, in response to cues such as nutrition or hormones, adapt their phenotype to environment. These responses may be divided into those for immediate benefit and those aimed at prediction of a future environment: disease occurs in the mismatch between predicted and realized future. The likely mechanisms that enable plasticity involve epigenetic processes, affecting the expression of genes associated with regulatory pathways. There is now evidence that epigenetic marks may be inherited and so contribute to non-genomic heritable disease risk. We end by discussing the global significance of the DOHaD phenomenon and its potential applications for public health purposes.
引用
收藏
页码:6 / 18
页数:13
相关论文
共 134 条
[1]   Developmental origins of disease and determinants of chromatin structure: maternal diet modifies the primate fetal epigenome [J].
Aagaard-Tillery, Kjersti M. ;
Grove, Kevin ;
Bishop, Jacalyn ;
Ke, Xingrao ;
Fu, Qi ;
McKnight, Robert ;
Lane, Robert H. .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2008, 41 (1-2) :91-102
[2]  
Aerts L, 1979, J Dev Physiol, V1, P219
[3]   Growth patterns and the risk of breast cancer in women [J].
Ahlgren, M ;
Melbye, M ;
Wohlfahrt, J ;
Sorensen, TIA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (16) :1619-1626
[4]  
Alderman H., 2004, Estimated Economic Benefits of Reducing Low Birth Weight in Low-Income Countries
[5]   The eukaryotic genome as an RNA machine [J].
Amaral, Paulo P. ;
Dinger, Marcel E. ;
Mercer, Tim R. ;
Mattick, John S. .
SCIENCE, 2008, 319 (5871) :1787-1789
[6]  
Amundson R, 2005, CAMB STUD PHIL BIOL, P1, DOI 10.1017/CBO9781139164856
[7]  
[Anonymous], TACKLING OBESITIES F
[8]  
[Anonymous], J DEV ORIGINS HLTH D, DOI DOI 10.1017/S2040174409990018
[9]  
[Anonymous], BRIT MED J
[10]   Epigenetic transgenerational actions of endocrine disruptors and mate fertility [J].
Anway, MD ;
Cupp, AS ;
Uzumcu, M ;
Skinner, MK .
SCIENCE, 2005, 308 (5727) :1466-1469