Bone modeling: the first step in the bone-building process
Bone modeling: the first step in the bone-building process
Osteoporosis is a major cause of morbidity and mortality through its association
with age-related fractures. Although most effort in fracture
prevention has been directed at retarding the rate of age-related bone
loss, and reducing the frequency and severity of trauma among elderly people,
evidence is growing that peak bone mass is an important contributor to bone
strength during later life. Bone mass in later life depends upon the peak attained
during childhood and adolescence, and on the subsequent rate of bone loss. Factors
that influence the accumulation of bone mineral during childhood and adolescence
include heredity, gender, diet, physical activity, endocrine status, and
sporadic risk factors such as cigarette smoking. In addition to modifiable factors
during childhood, evidence has also accrued that fracture risk might be programmed
during intrauterine life. Epidemiological studies have demonstrated
a relationship between birth weight, weight in infancy, and adult bone mass.
This appears to be mediated through modulation of the set-point for basal activity
of pituitary-dependent endocrine systems, such as the hypothalamic-pituitary-
adrenal axis, and the growth hormone/insulin-like growth factor I axis.
Maternal smoking, diet, and physical activity levels appear to modulate bone
mineral acquisition during intrauterine life. Furthermore, both low birth size
and poor childhood growth are directly linked to the later risk of hip fracture.
Optimization of maternal nutrition and intrauterine growth should also be included
in preventive strategies against osteoporotic fracture, albeit for future
generations.
osteoporosis, epidemiology, growth, programming, development
113-119
Cole, Z.A.
c070462a-a9c1-48a3-ad61-089e6fefa1a6
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
2007
Cole, Z.A.
c070462a-a9c1-48a3-ad61-089e6fefa1a6
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Cole, Z.A. and Cooper, C.
(2007)
Bone modeling: the first step in the bone-building process.
Medicographia, 29 (2), .
Abstract
Osteoporosis is a major cause of morbidity and mortality through its association
with age-related fractures. Although most effort in fracture
prevention has been directed at retarding the rate of age-related bone
loss, and reducing the frequency and severity of trauma among elderly people,
evidence is growing that peak bone mass is an important contributor to bone
strength during later life. Bone mass in later life depends upon the peak attained
during childhood and adolescence, and on the subsequent rate of bone loss. Factors
that influence the accumulation of bone mineral during childhood and adolescence
include heredity, gender, diet, physical activity, endocrine status, and
sporadic risk factors such as cigarette smoking. In addition to modifiable factors
during childhood, evidence has also accrued that fracture risk might be programmed
during intrauterine life. Epidemiological studies have demonstrated
a relationship between birth weight, weight in infancy, and adult bone mass.
This appears to be mediated through modulation of the set-point for basal activity
of pituitary-dependent endocrine systems, such as the hypothalamic-pituitary-
adrenal axis, and the growth hormone/insulin-like growth factor I axis.
Maternal smoking, diet, and physical activity levels appear to modulate bone
mineral acquisition during intrauterine life. Furthermore, both low birth size
and poor childhood growth are directly linked to the later risk of hip fracture.
Optimization of maternal nutrition and intrauterine growth should also be included
in preventive strategies against osteoporotic fracture, albeit for future
generations.
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Published date: 2007
Keywords:
osteoporosis, epidemiology, growth, programming, development
Identifiers
Local EPrints ID: 61007
URI: http://eprints.soton.ac.uk/id/eprint/61007
ISSN: 0243-3397
PURE UUID: eb447f0b-3f6c-4d98-894a-b7d3b882abc3
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Date deposited: 18 Nov 2008
Last modified: 18 Mar 2024 02:44
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Author:
Z.A. Cole
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