Abstract
Aging can be defined as deteriorative changes during postmaturational life that are associated with an increased risk of morbidity, disability and death. The process of human aging commences as early as conception with the inheritance of a specific genome, and does not cease until death. Environmental influences during intrauterine and early postnatal life modify gene expression with effects on phenotypes that persist into adulthood, and often result in a predisposition to age-related system decline. This developmental plasticity allows one genotype to give rise to a range of different physiological or morphological states in response to different prevailing environmental conditions during development. Thus, phenotypic alterations occur in response to environmental changes in just one generation. This plasticity has been shown to have specific effects on the musculoskeletal system. For example, lower weight at birth and at 1 year of age has been shown to be associated with a greater risk of osteoporosis and sarcopenia in later life. As an individual grows, the potential for plasticity reduces. Further research is required to obtain a full understanding of the lifecourse determinants of aging.
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Abbreviations
- BMC:
-
bone mineral content
- BMD:
-
bone mineral density
- DXA:
-
Dual-energy X-ray absorptiometry
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Acknowledgements
The authors are grateful to the Medical Research Council, the NIHR Biomedical Research Unit in Nutrition, University of Southampton, and the NIHR Biomedical Research Unit in Musculoskeletal Science, University of Oxford, for supporting this research. The manuscript was prepared by Mrs Gill Strange.
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Edwards, M., Dennison, E., Sayer, A.A., Cooper, C. (2012). Lifecourse Epidemiology and Aging. In: Newman, A., Cauley, J. (eds) The Epidemiology of Aging. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-5061-6_10
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