The association of type 2 diabetes-related characteristics with fracture risk at different sites


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The association of type 2 diabetes-related characteristics with fracture risk at different sites

Aim: To determine the association of diabetes-related characteristics with fractures at different sites in individuals with type 2 diabetes (T2D). Materials and

Methods: We conducted a cohort study using the Clinical Practice Research Datalink (CPRD) GOLD. Patients aged over 30 years with T2D were identified within the CPRD. Patients were followed from the start of diabetes treatment until the end of data collection, death, or the occurrence of a fracture. Cox proportional hazards models were used to estimate the hazard ratios for the association of the individual characteristics (diabetes duration, glycated haemoglobin [HbA1c] level, and microvascular complications) with fracture risk, adjusted for demographics, comorbidities and comedication.

Results: A diabetes duration of >10 years was associated with an increased risk of any fracture and major osteoporotic fractures (MOFs), while a diabetes duration of >8 years was associat ed with an increased hip fracture risk, compared to a duration <2 years. An HbA1c level <6% was associated with an increased fracture risk compared to HbA1c values of 6% to <7%. The presence of one or two microvascular complications was associated with an increased risk of any fracture and MOFs and the presence of two microvascular complications was associated with an increased hip fracture risk, compared to no microvascular complications.

Conclusion: In conclusion, our study shows that a diabetes duration of 10 years or more, strict glycaemic control resulting in HbA1c levels below 6%, and/or the presence of at least one microvascular complication increased the risk of any fracture, hip fractures, MOFs, and humerus fractures, but not ankle, scapula or skull fractures. © 2024 The Author(s). Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

Authors : van Hulten V.; Souverein P.C.; Starup-Linde J.; Viggers R.; Klungel O.H.; Vestergaard P.; Brouwers M.C.J.G.; van den Bergh J.P.; Driessen J.H.M.

Source : John Wiley and Sons Inc

Article Information

Year 2024
Type Article
DOI 10.1111/dom.15884
ISSN 14628902
Volume 26

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