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Serum fasting cortisol in relation to bone, and the role of genetic variations in the glucocorticoid receptor

Serum fasting cortisol in relation to bone, and the role of genetic variations in the glucocorticoid receptor
Serum fasting cortisol in relation to bone, and the role of genetic variations in the glucocorticoid receptor
Objective To examine the relationship between endogenous cortisol and bone, and the role of genetic variations in the glucocorticoid receptor (GR). Design and patients The Longitudinal Ageing Study Amsterdam (LASA), a population-based cohort study in older men and women. Measurements Serum fasting cortisol was assessed by competitive immunoassay (n = 1214); bone mineral density (BMD) by dual X-ray absorptiometry (DXA) (n = 502); broadband ultrasound attenuation (BUA) by ultrasound (n = 1209); fractures by self-report (n = 1211); and GR gene polymorphisms (ER22/23EK, N363S, 9beta, BclI) were genotyped by Taqman (n = 858). Results Higher serum fasting cortisol was significantly associated with lower BMD at all sites and BUA at the heel in women, although most relationships were attenuated by age and body mass index (BMI). The effect on femoral neck BMD remained statistically significant in the fully adjusted model (r = -0.135, P = 0.04). No significant associations in men were found. Female 9beta G-allele carriers had 50.2 nmol/l lower cortisol and 1.2 lower free cortisol levels than AA homozygotes [P = 0.01 for (free) cortisol]. Furthermore, female BclI GG homozygotes had 54.8 nmol/l higher cortisol levels than C-carriers (P = 0.03). In the total population, BclI GG homozygotes had 0.05 g/cm(2) lower trochanteric region BMD (P = 0.03). For the other GR gene polymorphisms, no significant associations were found. Conclusions Higher cortisol levels are associated with lower femoral neck BMD in elderly women. The G allele of the 9beta polymorphism was associated with lower serum cortisol levels in women. Female BclI GG homozygotes had higher serum cortisol levels, and BclI GG homozygotes had lower trochanteric region BMD in the total population.
cohort, women, bone, netherlands, elderly, female, cohort studies, ageing, cortisol, neck, body mass index, fasting, fractures
871-878
van Schoor, N.M.
54108e9a-d965-45e0-86a2-a5eccb7f2890
Dennison, E.
ee647287-edb4-4392-8361-e59fd505b1d1
Lips, P.
c17c31d2-f4d8-457f-99ad-fa5af27723ca
Uitterlinden, A.G.
e15f45d4-cdaf-4d8e-9f77-38e4cddd3c5a
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6
van Schoor, N.M.
54108e9a-d965-45e0-86a2-a5eccb7f2890
Dennison, E.
ee647287-edb4-4392-8361-e59fd505b1d1
Lips, P.
c17c31d2-f4d8-457f-99ad-fa5af27723ca
Uitterlinden, A.G.
e15f45d4-cdaf-4d8e-9f77-38e4cddd3c5a
Cooper, C.
e05f5612-b493-4273-9b71-9e0ce32bdad6

van Schoor, N.M., Dennison, E., Lips, P., Uitterlinden, A.G. and Cooper, C. (2007) Serum fasting cortisol in relation to bone, and the role of genetic variations in the glucocorticoid receptor. Clinical Endocrinology, 67 (6), 871-878. (doi:10.1111/j.1365-2265.2007.02978.x).

Record type: Article

Abstract

Objective To examine the relationship between endogenous cortisol and bone, and the role of genetic variations in the glucocorticoid receptor (GR). Design and patients The Longitudinal Ageing Study Amsterdam (LASA), a population-based cohort study in older men and women. Measurements Serum fasting cortisol was assessed by competitive immunoassay (n = 1214); bone mineral density (BMD) by dual X-ray absorptiometry (DXA) (n = 502); broadband ultrasound attenuation (BUA) by ultrasound (n = 1209); fractures by self-report (n = 1211); and GR gene polymorphisms (ER22/23EK, N363S, 9beta, BclI) were genotyped by Taqman (n = 858). Results Higher serum fasting cortisol was significantly associated with lower BMD at all sites and BUA at the heel in women, although most relationships were attenuated by age and body mass index (BMI). The effect on femoral neck BMD remained statistically significant in the fully adjusted model (r = -0.135, P = 0.04). No significant associations in men were found. Female 9beta G-allele carriers had 50.2 nmol/l lower cortisol and 1.2 lower free cortisol levels than AA homozygotes [P = 0.01 for (free) cortisol]. Furthermore, female BclI GG homozygotes had 54.8 nmol/l higher cortisol levels than C-carriers (P = 0.03). In the total population, BclI GG homozygotes had 0.05 g/cm(2) lower trochanteric region BMD (P = 0.03). For the other GR gene polymorphisms, no significant associations were found. Conclusions Higher cortisol levels are associated with lower femoral neck BMD in elderly women. The G allele of the 9beta polymorphism was associated with lower serum cortisol levels in women. Female BclI GG homozygotes had higher serum cortisol levels, and BclI GG homozygotes had lower trochanteric region BMD in the total population.

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More information

Published date: December 2007
Keywords: cohort, women, bone, netherlands, elderly, female, cohort studies, ageing, cortisol, neck, body mass index, fasting, fractures

Identifiers

Local EPrints ID: 61576
URI: http://eprints.soton.ac.uk/id/eprint/61576
PURE UUID: 7a89d27f-3c38-45bd-8353-f362e3077b96
ORCID for E. Dennison: ORCID iD orcid.org/0000-0002-3048-4961
ORCID for C. Cooper: ORCID iD orcid.org/0000-0003-3510-0709

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Date deposited: 02 Oct 2008
Last modified: 18 Mar 2024 02:44

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Contributors

Author: N.M. van Schoor
Author: E. Dennison ORCID iD
Author: P. Lips
Author: A.G. Uitterlinden
Author: C. Cooper ORCID iD

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