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Journal of bone and mineral research, 2007-12, Vol.22 (12), p.1878-1884
2007
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Autor(en) / Beteiligte
Titel
Does Diabetes Increase the Risk for Fractures After Solid Organ Transplantation? A Nested Case‐Control Study
Ist Teil von
  • Journal of bone and mineral research, 2007-12, Vol.22 (12), p.1878-1884
Ort / Verlag
Washington, DC: John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR)
Erscheinungsjahr
2007
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
  • To assess the risk of fractures after a solid organ transplantation among diabetic versus nondiabetic patients, we conducted a nested case‐control study. Pretransplant diabetes was associated with a 2‐fold increase in post‐transplant fractures. Introduction: Diabetes has been associated with osteoporosis in the general population. However, among patients receiving solid organ transplantation, the association between pretransplant diabetes and post‐transplant fractures is not clear, although both diabetes and fractures are prevalent among this patient population. We aimed to determine whether pretransplant diabetes increases the risk of fractures among patients receiving solid organ transplantation. Materials and Methods: We conducted a nested case‐control study in a cohort of subjects 18 years and older, enrolled in the Quebec Drug Insurance Plan, who received a first solid organ transplantation between January 1986 and December 2005. Cases had sustained a fracture between the date of discharge from the hospitalization for solid organ transplantation and the end of the study period. All remaining patients were eligible controls. The fracture date was the case index date. Cases were matched to up to four controls on the type of organ transplanted and the date of transplantation. The index date of a control patient was that of his/her matched case. Crude and adjusted ORs were obtained with univariate and multivariate conditional logistic regression models. Results: The study included 238 cases and 873 controls. Pretransplant diabetes was present in 30% of the cases and 22% of the controls (crude OR: 2.16; 95% CI: 1.7–2.8). After adjusting for age, sex, previous fractures, past hyperthyroidism, hospitalization duration, use of narcotics, benzodiazepines, antidepressants, loop diuretics, thiazide diuretics, glucocorticoids, immunosuppressants, estrogens, bisphosphonates, calcium, vitamin D, and calcitonin, pretransplantation diabetes remained a significant risk factor for fractures (adjusted OR: 1.94; 95% CI: 1.5–2.6). Use of narcotics (OR: 3.0; 95% CI: 2.0–4.4) and antidepressants (OR: 1.9; 95% CI: 1.2–3.1) in the month preceding the index date and use of loop diuretics in the year preceding the index date (OR: 1.4; 95% CI: 1.1–1.9) were also associated with increased risks of fractures. Conclusions: Pretransplant diabetes seemed to significantly increase post‐transplant fractures among adults receiving solid organ transplantation. Pretransplant fracture prophylaxis should be considered in these patients.

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