Journal article icon

Journal article

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

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.
Publication status:
Published

Actions


Access Document


Publisher copy:
10.1111/j.1365-2265.2007.02978.x

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Role:
Author


Journal:
Clinical endocrinology More from this journal
Volume:
67
Issue:
6
Pages:
871-878
Publication date:
2007-12-01
DOI:
EISSN:
1365-2265
ISSN:
0300-0664


Language:
English
Keywords:
Pubs id:
pubs:125696
UUID:
uuid:70c13a43-64a6-43ee-b182-99218cf2411e
Local pid:
pubs:125696
Source identifiers:
125696
Deposit date:
2012-12-19

Terms of use



Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP