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Umbilical venous IGF-1 concentration, neonatal bone mass, and body composition

Umbilical venous IGF-1 concentration, neonatal bone mass, and body composition
Umbilical venous IGF-1 concentration, neonatal bone mass, and body composition
IGF-1 is a key growth factor during fetal life. Using DXA, we found that the concentration of IGF-1 in umbilical cord serum is strongly related to neonatal whole body bone mineral content, lean mass, and fat mass. However IGF-1 did not explain the relationships of maternal smoking, fat mass, and physical activity with neonatal bone mass. The study supports a direct role for circulating IGF-1 in growth of the fetal skeleton.
INTRODUCTION: Evidence is accumulating that the risk of osteoporosis in later life may be determined in part by environmental influences during intrauterine and early postnatal life. We previously reported that maternal birthweight, smoking, fat stores, and physical activity during pregnancy predict neonatal bone mass. While the growth hormone/insulin-like growth factor 1 (GH/IGF-1) axis is an important determinant of postnatal skeletal growth, there are few data relating the concentration of growth factors in umbilical cord blood to bone mineral content (BMC) and other indices of body composition in the newborn infant.
MATERIALS AND METHODS: We conducted a population-based study in a cohort of full-term, newborn infants whose mothers were characterized for lifestyle, body composition, and nutrition through their normal pregnancies. In a sample of 119 infants from the cohort, we related cord serum IGF-1 and insulin-like growth factor binding protein (IGFBP)-3 concentrations to neonatal body composition measured by DXA and evaluated the extent to which this cytokine mediates the previously reported effects of maternal diet and lifestyle on neonatal bone mass.
RESULTS: There were strong positive associations between cord serum IGF-1 concentration and whole body BMC (r = 0.38, p < 0.001), whole body lean mass (r = 0.40, p < 0.001), and whole body fat mass (r = 0.50, p < 0.001) after adjusting for gestational age and sex. There was no association between cord serum IGF-1 and BMC adjusted for bone size. Neither cord serum IGF-1 nor IGFBP-3 explained the relationships that we previously reported between maternal influences and neonatal bone mass.
CONCLUSIONS: Cord serum IGF-1 is more closely related to the size of the neonatal skeleton than to its degree of mineralization. Documented maternal determinants of neonatal bone mass seem to mediate their effects independently of variations in cord serum IGF-1 in healthy pregnancies.
osteoporosis, programming, epidemiology, growth, bone mass
0884-0431
56-63
Javaid, M.K.
51d3310b-032e-4c15-83ac-b878bce090f3
Godfrey, K.M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
Taylor, P.
28b91e71-fad2-4375-8a1e-535f861901c3
Shore, S.R.
2d6b826f-a5e7-4bc0-ae12-3664df6e2aa1
Breier, B.
e413f910-b49c-45e7-b69b-886729ed6f78
Arden, N.K.
23af958d-835c-4d79-be54-4bbe4c68077f
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
Javaid, M.K.
51d3310b-032e-4c15-83ac-b878bce090f3
Godfrey, K.M.
0931701e-fe2c-44b5-8f0d-ec5c7477a6fd
Taylor, P.
28b91e71-fad2-4375-8a1e-535f861901c3
Shore, S.R.
2d6b826f-a5e7-4bc0-ae12-3664df6e2aa1
Breier, B.
e413f910-b49c-45e7-b69b-886729ed6f78
Arden, N.K.
23af958d-835c-4d79-be54-4bbe4c68077f
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6

Javaid, M.K., Godfrey, K.M., Taylor, P., Shore, S.R., Breier, B., Arden, N.K. and Cooper, C. (2004) Umbilical venous IGF-1 concentration, neonatal bone mass, and body composition. Journal of Bone and Mineral Research, 19 (1), 56-63. (doi:10.1359/JBMR.0301211).

Record type: Article

Abstract

IGF-1 is a key growth factor during fetal life. Using DXA, we found that the concentration of IGF-1 in umbilical cord serum is strongly related to neonatal whole body bone mineral content, lean mass, and fat mass. However IGF-1 did not explain the relationships of maternal smoking, fat mass, and physical activity with neonatal bone mass. The study supports a direct role for circulating IGF-1 in growth of the fetal skeleton.
INTRODUCTION: Evidence is accumulating that the risk of osteoporosis in later life may be determined in part by environmental influences during intrauterine and early postnatal life. We previously reported that maternal birthweight, smoking, fat stores, and physical activity during pregnancy predict neonatal bone mass. While the growth hormone/insulin-like growth factor 1 (GH/IGF-1) axis is an important determinant of postnatal skeletal growth, there are few data relating the concentration of growth factors in umbilical cord blood to bone mineral content (BMC) and other indices of body composition in the newborn infant.
MATERIALS AND METHODS: We conducted a population-based study in a cohort of full-term, newborn infants whose mothers were characterized for lifestyle, body composition, and nutrition through their normal pregnancies. In a sample of 119 infants from the cohort, we related cord serum IGF-1 and insulin-like growth factor binding protein (IGFBP)-3 concentrations to neonatal body composition measured by DXA and evaluated the extent to which this cytokine mediates the previously reported effects of maternal diet and lifestyle on neonatal bone mass.
RESULTS: There were strong positive associations between cord serum IGF-1 concentration and whole body BMC (r = 0.38, p < 0.001), whole body lean mass (r = 0.40, p < 0.001), and whole body fat mass (r = 0.50, p < 0.001) after adjusting for gestational age and sex. There was no association between cord serum IGF-1 and BMC adjusted for bone size. Neither cord serum IGF-1 nor IGFBP-3 explained the relationships that we previously reported between maternal influences and neonatal bone mass.
CONCLUSIONS: Cord serum IGF-1 is more closely related to the size of the neonatal skeleton than to its degree of mineralization. Documented maternal determinants of neonatal bone mass seem to mediate their effects independently of variations in cord serum IGF-1 in healthy pregnancies.

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Published date: 2004
Keywords: osteoporosis, programming, epidemiology, growth, bone mass

Identifiers

Local EPrints ID: 25667
URI: http://eprints.soton.ac.uk/id/eprint/25667
ISSN: 0884-0431
PURE UUID: 42b68511-eda5-4fc0-9988-e969389fa838
ORCID for K.M. Godfrey: ORCID iD orcid.org/0000-0002-4643-0618
ORCID for C. Cooper: ORCID iD orcid.org/0000-0003-3510-0709

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Date deposited: 20 Apr 2006
Last modified: 18 Mar 2024 02:44

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Contributors

Author: M.K. Javaid
Author: K.M. Godfrey ORCID iD
Author: P. Taylor
Author: S.R. Shore
Author: B. Breier
Author: N.K. Arden
Author: C. Cooper ORCID iD

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