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Published on: January 29, 2018
Association between CKD-MBD and hip-bone microstructures in dialysis patients
Ken Iseri1,2, Masahide Mizobuchi3, Kanji Shishido4
1Department of Clinical Pharmacy, Division of Clinical Research and Development, School of Pharmacy, Showa University, Tokyo, Japan.
Insights
Elevated parathyroid hormone (PTH) levels, not low PTH, are linked to worsening hip bone microstructures in dialysis patients. Managing PTH is crucial for preserving bone health in this population.
Area of Science:
- Nephrology
- Orthopedics
- Bone Metabolism
Background:
- Longitudinal changes in hip bone microstructures and strength in dialysis patients are not well understood.
- The impact of chronic kidney disease-mineral and bone disorder (CKD-MBD) biomarkers on these bone changes requires further investigation.
Purpose of the Study:
- To examine longitudinal changes in hip bone microstructures and estimated bone strength in dialysis patients.
- To investigate the associations between time-dependent CKD-MBD biomarkers and bone health metrics.
Main Methods:
- Retrospective study of 276 dialysis patients over up to 2.5 years.
- Utilized 3D-SHAPER software to assess cortical and trabecular bone compartments and bone strength indices.
- Employed multivariate mixed models to analyze associations between CKD-MBD biomarkers and bone metrics.
Main Results:
- Significant decreases observed in areal bone mineral density (aBMD), volumetric BMD (vBMD), cortical thickness, and cortical surface BMD (sBMD).
- Estimated bone strength indices including cross-sectional area (CSA), CSMI, SM, and buckling ratio also deteriorated.
- Elevated intact-parathyroid hormone (i-PTH) showed significant inverse correlations with multiple bone parameters and strength indices, while serum calcium and phosphate levels did not.
Conclusions:
- Elevated PTH levels, rather than low PTH, are associated with the deterioration of hip bone microstructures in dialysis patients.
- Effective management of PTH levels is critical for maintaining hip bone microstructure in patients undergoing dialysis.
Background:
The longitudinal changes in hip-bone microstructures and estimated bone strength in dialysis patients, and the impact of chronic kidney disease-mineral and bone disorder (CKD-MBD) biomarkers on these changes, remain insufficiently explored.
Methods:
This retrospective study examined changes in cortical and trabecular bone compartments and estimated bone-strength indices, obtained by using 3D-SHAPER software, in the hip regions of 276 dialysis patients over up to 2.5 years. We used multivariate mixed models to investigate the associations between time-dependent CKD-MBD biomarkers and bone health metrics.
Results:
There was a significant decrease in areal bone mineral density (aBMD), integral volumetric BMD (vBMD), trabecular vBMD, cortical thickness and cortical surface BMD (sBMD). Similar deteriorations were found in estimated bone-strength indices [cross-sectional area (CSA), cross-sectional moment of inertia (CSMI), section modulus (SM) and buckling ratio]. Neither serum calcium nor phosphate levels were significantly associated with changes in three-dimensional parameters or estimated bone-strength indices. In contrast, serum alkaline phosphatase levels showed a significant inverse correlation with aBMD and CSA. The intact-parathyroid hormone (i-PTH) was significantly inversely correlated with aBMD, integral vBMD, trabecular vBMD, cortical thickness, cortical vBMD, CSA, CSMI and SM. When applying the KDIGO criteria as a sensitivity analysis, the higher PTH group had significant negative associations with aBMD, integral vBMD, cortical vBMD, cortical thickness and cortical sBMD. Notably, the lower PTH group showed a positive significant correlation with integral vBMD and trabecular vBMD.
Conclusions:
Elevated PTH, not low PTH, was associated with deterioration of hip-bone microstructures. Better management of PTH levels may play a crucial role in the hip-bone microstructure in dialysis patients.
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