Epigenetic influences in the developmental origins of osteoporosis
Epigenetic influences in the developmental origins of osteoporosis
Osteoporosis is a major public health problem due to consequent fragility fractures; data from the UK suggest that up to 50% of women and 20% men aged 50 years will have an osteoporosis-related fracture in their remaining lifetime. Skeletal size and density increase from early embryogenesis through intrauterine, infant, childhood and adult life to reach a peak in the third to fourth decade. The peak bone mass achieved is a strong predictor of later osteoporosis risk. Epidemiological studies have demonstrated a positive relationship between early growth and later bone mass, both at peak and in later life, and also with reduced risk of hip fracture. Mother–offspring cohorts have allowed the elucidation of some of the specific factors in early life, such as maternal body build, lifestyle and 25(OH)-vitamin D status, which might be important. Most recently, the phenomenon of developmental plasticity, whereby a single genotype may give rise to different phenotypes depending on the prevailing environment, and the science of epigenetics have presented novel molecular mechanisms which may underlie previous observations. This review will give an overview of these latter developments in the context of the burden of osteoporosis and the wider data supporting the link between the early environment and bone health in later life.
developmental origins, epigenetic, osteoporosis
401-410
Holroyd, C.
d08021f2-c96e-45b0-83b7-b5ce6a497a19
Harvey, N.
ce487fb4-d360-4aac-9d17-9466d6cba145
Dennison, E.M.
ee647287-edb4-4392-8361-e59fd505b1d1
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
February 2012
Holroyd, C.
d08021f2-c96e-45b0-83b7-b5ce6a497a19
Harvey, N.
ce487fb4-d360-4aac-9d17-9466d6cba145
Dennison, E.M.
ee647287-edb4-4392-8361-e59fd505b1d1
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Holroyd, C., Harvey, N., Dennison, E.M. and Cooper, C.
(2012)
Epigenetic influences in the developmental origins of osteoporosis.
Osteoporosis International, 23 (2), .
(doi:10.1007/s00198-011-1671-5).
(PMID:21656266)
Abstract
Osteoporosis is a major public health problem due to consequent fragility fractures; data from the UK suggest that up to 50% of women and 20% men aged 50 years will have an osteoporosis-related fracture in their remaining lifetime. Skeletal size and density increase from early embryogenesis through intrauterine, infant, childhood and adult life to reach a peak in the third to fourth decade. The peak bone mass achieved is a strong predictor of later osteoporosis risk. Epidemiological studies have demonstrated a positive relationship between early growth and later bone mass, both at peak and in later life, and also with reduced risk of hip fracture. Mother–offspring cohorts have allowed the elucidation of some of the specific factors in early life, such as maternal body build, lifestyle and 25(OH)-vitamin D status, which might be important. Most recently, the phenomenon of developmental plasticity, whereby a single genotype may give rise to different phenotypes depending on the prevailing environment, and the science of epigenetics have presented novel molecular mechanisms which may underlie previous observations. This review will give an overview of these latter developments in the context of the burden of osteoporosis and the wider data supporting the link between the early environment and bone health in later life.
This record has no associated files available for download.
More information
e-pub ahead of print date: 9 May 2011
Published date: February 2012
Keywords:
developmental origins, epigenetic, osteoporosis
Organisations:
Faculty of Health Sciences
Identifiers
Local EPrints ID: 336625
URI: http://eprints.soton.ac.uk/id/eprint/336625
ISSN: 0937-941X
PURE UUID: da2127ec-b9e5-4031-9c78-a770c013fce5
Catalogue record
Date deposited: 02 Apr 2012 15:47
Last modified: 18 Mar 2024 02:58
Export record
Altmetrics
Contributors
Author:
C. Holroyd
Download statistics
Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.
View more statistics