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. 2009 Jun;20(6):923-33.
doi: 10.1007/s00198-008-0763-3. Epub 2008 Oct 2.

Poor glycemic control is associated with low BMD detected in premenopausal women with type 1 diabetes

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Poor glycemic control is associated with low BMD detected in premenopausal women with type 1 diabetes

K K Danielson et al. Osteoporos Int. 2009 Jun.

Abstract

Summary: The etiology of bone fragility in individuals with type 1 diabetes is unknown. This study demonstrated that bone turnover favors resorption and that poor glycemic control is associated with low bone mineral density (BMD) and low bone turnover, in premenopausal women with type 1 diabetes. The results could inform future interventions.

Introduction: Low BMD and fracture may be complications of type 1 diabetes. We sought to determine the roles of bone turnover and glycemic control in the etiology of low BMD.

Methods: Premenopausal women from the Wisconsin Diabetes Registry Study and matched controls were compared (n = 75 pairs). Heel and forearm BMD were measured, and hip and spine BMD were measured in a subset. Markers of bone formation (osteocalcin) and resorption (NTx), and glycemic control (HbA1c) were determined.

Results: Age ranged from 18 to 50 years with a mean of 28, and 97% were Non-Hispanic white. Among women with diabetes, mean disease duration was 16 years and current HbA1c was 8%. Compared to controls, women with diabetes had a high prevalence of previous fracture (37% vs. 24%) and low BMD for age (heel or forearm: 49% vs. 31%), low heel and forearm BMD, and low osteocalcin levels. Levels of NTx were similar, suggesting uncoupled turnover favoring resorption. Poor glycemic control was associated with low BMD at all bone sites except the spine, and with low osteocalcin and NTx levels.

Conclusions: Optimal glycemic control may prevent low BMD and altered bone turnover in type 1 diabetes, and decrease fracture risk.

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Figures

Figure 1
Figure 1
Individual levels of bone turnover markers for 75 premenopausal women with type 1 diabetes (points jittered horizontally). Each level is expressed as a Z-score (number of SDs from the mean of 75 matched controls). The Uncoupling Index was calculated as the osteocalcin Z-score minus NTx Z-score. Lines with respective numbers are mean Z-scores or the UncouplingIndex. *p<0.05 statistical significance of the mean Z-score or Uncoupling Index compared to zero as assessed by one-group t-test.

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