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Published on: August 17, 2017
Risk factors for hip and vertebral fractures in chronic kidney disease: the CRIC study
Simon Hsu1, Nisha Bansal1, Michelle Denburg2,3
1Division of Nephrology and Kidney Research Institute, Department of Medicine, University of Washington, Seattle, WA 98195, United States.
Insights
Fracture risk is elevated in chronic kidney disease (CKD). Lower kidney function, diabetes, and higher parathyroid hormone levels increase fracture risk, highlighting potential modifiable factors.
Area of Science:
- Nephrology
- Orthopedics
- Epidemiology
Background:
- Fracture risk is significantly higher in individuals with chronic kidney disease (CKD) compared to the general population.
- The underlying causes and specific risk factors for fractures in CKD may differ from those in non-CKD populations.
Purpose of the Study:
- To investigate the associations between various risk factors and the incidence of hip or vertebral fractures in a cohort of patients with CKD.
- To identify specific clinical and biochemical markers associated with increased fracture risk in this population.
Main Methods:
- A cohort study of 3939 participants in the Chronic Renal Insufficiency Cohort (CRIC) was conducted.
- Cox regression analysis was used to assess the association of baseline and time-updated risk factors with hip or vertebral fractures.
- Fractures were identified using hospital discharge codes over a mean follow-up of 11.1 years.
Main Results:
- Lower estimated glomerular filtration rate (eGFR), diabetes, lower body mass index (BMI), steroid use, proteinuria, and elevated parathyroid hormone (PTH) were associated with increased fracture risk.
- Lower time-updated serum calcium and bicarbonate concentrations were also linked to higher fracture incidence.
- Kidney failure treated with dialysis showed the highest fracture risk (HR 4.53), followed by post-kidney transplantation (HR 2.48), compared to eGFR ≥60.
Conclusions:
- Reduced kidney function (lower eGFR) is a significant risk factor for fractures in CKD patients, with the highest risk observed in kidney failure.
- Several factors including diabetes, low BMI, steroid use, proteinuria, high PTH, and low calcium/bicarbonate levels are associated with fractures and may represent modifiable targets for intervention.
Abstract:
Fracture risk is high in chronic kidney disease (CKD) and underlying pathophysiology and risk factors may differ from the general population. In a cohort study of 3939 participants in the chronic renal insufficiency cohort (CRIC), we used Cox regression to test associations of putative risk factors with the composite of first hip or vertebral fracture assessed using hospital discharge codes. Mean age was 58 years, 45% were female, 42% were Black, and 13% were Hispanic. There were 82 hip and 24 vertebral fractures over a mean (SD) 11.1 (4.8) years (2.4 events per 1000 person-years [95% CI: 2.0, 2.9]). Measured at baseline, diabetes, lower body mass index (BMI), steroid use, proteinuria, and elevated parathyroid hormone (PTH) were each associated with fracture risk after adjusting for covariates. Lower time-updated estimated glomerular filtration rate (eGFR) was associated with fractures (HR 1.20 per 10 mL/min/1.73m2 lower eGFR; 95% CI: 1.04, 1.38) as were lower time-updated serum calcium and bicarbonate concentrations. Among time-updated categories of kidney function, hazard ratios (95% CI) for incident fracture were 4.53 (1.77, 11.60) for kidney failure treated with dialysis and 2.48 (0.86, 7.14) for post-kidney transplantation, compared with eGFR ≥60. Proton pump inhibitor use, dietary calcium intake, measures of vitamin D status, serum phosphate, urine calcium and phosphate, and plasma fibroblast growth factor-23 were not associated with fracture risk. In conclusion, lower eGFR in CKD is associated with higher fracture risk, which was highest in kidney failure. Diabetes, lower BMI, steroid use, proteinuria, higher serum concentrations of PTH, and lower calcium and bicarbonate concentrations were associated with fractures and may be modifiable risk factors.
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