Mechanisms of disease: in utero programming in the pathogenesis of hypertension
Mechanisms of disease: in utero programming in the pathogenesis of hypertension
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.
700-707
Barker, David J.P.
5c773838-b094-4ac1-999b-b5869717f243
Bagby, Susan P.
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Hanson, Mark A.
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December 2006
Barker, David J.P.
5c773838-b094-4ac1-999b-b5869717f243
Bagby, Susan P.
bf742bb6-21f7-4da8-96fa-d21ed1d20fd9
Hanson, Mark A.
1952fad1-abc7-4284-a0bc-a7eb31f70a3f
Barker, David J.P., Bagby, Susan P. and Hanson, Mark A.
(2006)
Mechanisms of disease: in utero programming in the pathogenesis of hypertension.
Nature Clinical Practice Nephrology, 2 (12), .
(doi:10.1038/ncpneph0344).
Abstract
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.
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Published date: December 2006
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Local EPrints ID: 60885
URI: http://eprints.soton.ac.uk/id/eprint/60885
ISSN: 1745-8323
PURE UUID: f4449bfe-1e59-497d-9a14-5c128261d2e3
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Date deposited: 22 Sep 2008
Last modified: 16 Mar 2024 03:17
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Author:
David J.P. Barker
Author:
Susan P. Bagby
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