Mechanisms of Disease:: in utero programming in the pathogenesis of hypertension

被引:193
作者
Barker, David J. P.
Bagby, Susan P.
Hanson, Mark A.
机构
[1] Univ Southampton, Dev Origins Hlth & Dis Div, Southampton SO9 5NH, Hants, England
[2] Oregon Hlth & Sci Univ, Dept Med, Heart Res Ctr, Portland, OR 97201 USA
来源
NATURE CLINICAL PRACTICE NEPHROLOGY | 2006年 / 2卷 / 12期
关键词
birth weight; developmental plasticity; hypertension;
D O I
10.1038/ncpneph0344
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Nutritional and other environmental cues during development can permanently alter the structure, homeostatic systems, and functions of the body. This phenomenon has been referred to as 'programming' Epidemiological and animal studies show that programmed effects operate within the normal range of growth and development, and influence the risk of chronic disease in adult life. We review the evidence that these effects include reduced nephron number and compensatory adaptations, which might lead to hypertension, and perhaps accelerate the decline in renal function that accompanies aging. These processes might be exacerbated by programmed changes in vascular structure and function, and alterations in endocrine and metabolic homeostasis. Programmed effects might be initiated as early as the periconceptual phase of development, and could involve epigenetic changes in gene expression or altered stem cell allocation. Better understanding of these processes could lead to the development of novel diagnostic and preventive measures, and to early detection of at-risk individuals. By monitoring blood pressure, weight, and renal function in children, it might be possible to reduce the risk of cardiovascular and renal disease in later life.
引用
收藏
页码:700 / 707
页数:8
相关论文
共 85 条
[1]   CARDIAC-OUTPUT AND UTEROPLACENTAL BLOOD-FLOW IN DIET-RESTRICTED AND DIET-REPLETED PREGNANT RATS [J].
AHOKAS, RA ;
ANDERSON, GD ;
LIPSHITZ, J .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1983, 146 (01) :6-13
[2]   Renal denervation abolishes hypertension in low-birth-weight offspring from pregnant rats with reduced uterine perfusion [J].
Alexander, BT ;
Hendon, AE ;
Ferril, G ;
Dwyer, TM .
HYPERTENSION, 2005, 45 (04) :754-758
[3]   Cardiovascular reactivity to stress and left ventricular mass in youth [J].
Allen, MT ;
Matthews, KA ;
Sherman, FS .
HYPERTENSION, 1997, 30 (04) :782-787
[4]  
BARKER DJP, 1989, LANCET, V2, P577
[5]   FETAL ORIGINS OF CORONARY HEART-DISEASE [J].
BARKER, DJP .
BRITISH MEDICAL JOURNAL, 1995, 311 (6998) :171-174
[6]   Fetal origins of adult disease:: strength of effects and biological basis [J].
Barker, DJP ;
Eriksson, JG ;
Forsén, T ;
Osmond, C .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2002, 31 (06) :1235-1239
[7]   Growth and living conditions in childhood and hypertension in adult life:: a longitudinal study [J].
Barker, DJP ;
Forsén, T ;
Eriksson, JG ;
Osmond, C .
JOURNAL OF HYPERTENSION, 2002, 20 (10) :1951-1956
[8]  
BARKER DJP, IN PRESS BMJ
[9]   Developmental plasticity and human health [J].
Bateson, P ;
Barker, D ;
Clutton-Brock, T ;
Deb, D ;
D'Udine, B ;
Foley, RA ;
Gluckman, P ;
Godfrey, K ;
Kirkwood, T ;
Lahr, MM ;
McNamara, J ;
Metcalfe, NB ;
Monaghan, P ;
Spencer, HG ;
Sultan, SE .
NATURE, 2004, 430 (6998) :419-421
[10]   Fetal experience and good adult design [J].
Bateson, P .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2001, 30 (05) :928-934