Bone mineral density and its determinants in diabetes: the Fremantle Diabetes Study |
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Authors: | V. Rakic W. A. Davis S. A. P. Chubb F. M. A. Islam R. L. Prince T. M. E. Davis |
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Affiliation: | (1) University of Western Australia, School of Medicine and Pharmacology, Fremantle Hospital, P.O. Box 480, Fremantle, WA, 6959, Australia;(2) Biochemistry Department, Fremantle Hospital, Fremantle, WA, Australia;(3) Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, WA, Australia;(4) University of Western Australia, School of Medicine and Pharmacology, Sir Charles Gairdner Hospital, Nedlands, WA, Australia |
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Abstract: | Aims/hypothesis We assessed the effects of type 1 and type 2 diabetes on bone density and metabolism.Materials and methods We analysed bone mineral density (BMD) measured at the hip, spine and forearm using dual energy X-ray absorptiometry in 34 patients with type 1 and 194 patients with type 2 diabetes. Patients were from the community-based Fremantle Diabetes Study, and findings for them were compared with those from normal age- and sex-matched control subjects from the local community. Biochemical and hormonal markers of bone metabolism were measured in a subset of 70 patients.Results After adjusting for age and BMI, there was a lower BMD at total hip (p<0.001) and femoral neck (p=0.012) in type 1 men vs control subjects, but type 1 women and matched controls had similar BMD at each site. There was a higher BMD at total hip (p=0.006), femoral neck (p=0.026) and forearm (p<0.001) in type 2 women vs control subjects, but diabetes status was not associated with BMD in type 2 men after adjustment for age and BMI. Serum oestradiol, BMI, C-terminal telopeptide of collagen type 1 and male sex were consistently and independently associated with BMD at forearm, hip and femoral neck and explained 61, 55 and 50% of the total variance in BMD, respectively, at these sites. Spine BMD was independently associated with BMI and ln(oestradiol).Conclusions/interpretation Men with type 1 diabetes may be at increased risk of osteoporosis, while type 2 women appear to be protected even after adjusting for BMI. Low serum oestradiol concentrations may predispose to diabetes-associated osteoporosis regardless of sex. |
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Keywords: | Bone mineral density Bone turnover markers Diabetes mellitus Dual energy X-ray absorptiometry Sex hormones |
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