Longer duration of diabetes strongly impacts fracture risk assessment: The Manitoba BMD cohort
Majumdar, Sumit R., Leslie, William D., Lix, Lisa M., Morin, Suzanne N., Johansson, Helena, Oden, Anders, McCloskey, Eugene V. and Kanis, John A.. (2016) Longer duration of diabetes strongly impacts fracture risk assessment: The Manitoba BMD cohort. Journal of Clinical Endocrinology and Metabolism. 101(11), pp. 4489 - 4496. https://doi.org/10.1210/jc.2016-2569
|Authors||Majumdar, Sumit R., Leslie, William D., Lix, Lisa M., Morin, Suzanne N., Johansson, Helena, Oden, Anders, McCloskey, Eugene V. and Kanis, John A.|
Context: Type 2 diabetes is associated with a higher risk for major osteoporotic fracture ( MOF ) and hip fracture than predicted by the World Health Organization fracture risk assessment ( FRAX ) tool. Objective: The objective of the study was to examine the impact of diabetes duration on fracture risk. Methods: Using a clinical dual-energy x-ray absorptiometry registry linked with the Manitoba administrative databases, we identified all women age 40 years or older with 10 or more years of prior health care coverage undergoing hip dual-energy x-ray absorptiometry measurements ( 1996–2013 ). Incident MOF and incident hip fractures were each studied over 7 years. Cox proportional hazards models were adjusted for FRAX ( FRAX adjusted ) and then FRAX plus comorbidity, falls, osteoporosis therapy, or insulin ( fully adjusted ). FRAX calibration was assessed comparing observed vs predicted probabilities. Results: There were 49 098 women without and 8840 women with diabetes ( 31.4% > 10 y duration; 20.1% 5–10 y; 23.7% < 5 y; 24.8% new onset ). In FRAX-adjusted analyses, only duration longer than 10 years was associated with a higher risk for MOF ( hazard ratio [HR] 1.47, 95% confidence interval [CI] 1.30–1.66 ), and this was similar in the fully adjusted models ( HR 1.34, 95% CI 1.17–1.54 ). In contrast, a higher risk for hip fracture was seen for all durations in a dose-dependent fashion ( eg, FRAX adjusted HR 2.10, 95% CI 1.71–2.59 for duration > 10 y vs HR 1.32, 95% CI 1.03–1.69 for new onset ). FRAX significantly underestimated the MOF risk ( calibration ratio 1.24, 95% CI 1.08–1.39 ) and hip fracture risk ( 1.93, 95% CI 1.50–2.35 ) in those with a diabetes duration longer than 10 years. Conclusion: Diabetes is a FRAX-independent risk factor for MOF only in women with a long duration of diabetes, but diabetes increases hip fracture risk, regardless of duration. Those with diabetes longer than 10 years are at particularly high risk of fracture, and this elevated risk is currently underestimated by FRAX.
|Journal||Journal of Clinical Endocrinology and Metabolism|
|Journal citation||101 (11), pp. 4489 - 4496|
|Digital Object Identifier (DOI)||https://doi.org/10.1210/jc.2016-2569|
|Open access||Open access|
|Page range||4489 - 4496|
|Research Group||Institute for Health and Ageing|
Copyright © 2016 by the Endocrine Society. This article is published under the terms of the Creative Commons Attribution-Non Commercial License (CC-BY-NC; http://creativecommons.org/licenses/by-nc/4.0/).
|Place of publication||United States|
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