4.7 Article

Mineral Metabolism and Cortical Volumetric Bone Mineral Density in Childhood Chronic Kidney Disease

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 98, Issue 5, Pages 1930-1938

Publisher

ENDOCRINE SOC
DOI: 10.1210/jc.2012-4188

Keywords

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Funding

  1. National Institutes of Health [R01-DK060030, R01-HD040714, K24-DK076808]
  2. National Center for Research Resources [UL1RR024134]
  3. National Center for Advancing Translational Sciences [UL1TR000003]
  4. National Kidney Foundation/Amgen Kidney Disease Outcomes Quality Initiative Research Fellowship
  5. Nephcure Foundation-American Society of Nephrology Research Grant
  6. [K23DK093556]

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Context: The relationships among cortical volumetric bone mineral density (CortBMD) and comprehensive measures of mineral metabolism have not been addressed in chronic kidney disease (CKD). Objective: The aim of the study was to identify the determinants of CortBMD in childhood CKD. A secondary objective was to assess whether CortBMD was associated with subsequent fracture. Design and Participants: This prospective cohort study included 171 children, adolescents, and young adults (aged 5-21 years) with CKD stages 2-5D at enrollment and 89 1 year later. Outcomes: Serum measures included vitamin D [25-hydroxyvitamin D (25[OH]D), 1,25-dihydroxyvitamin D (1,25(OH)(2)D), 24,25-dihydroxyvitamin D], vitamin D-binding protein, intact PTH, fibroblast growth factor 23, calcium, and phosphorus. Tibia quantitative computed tomography measures of CortBMD were expressed as sex-, race-, and age-specific Z-scores based on 675 controls. Multivariable linear regression identified the independent correlates of CortBMD Z-scores and the change in CortBMD Z-scores. Results: Lower calcium (beta = .31/1 mg/dL, P = .01) and 25(OH)D (beta = .18/10 ng/mL, P = .04) and higher PTH (beta = -.02/10%, P = .002) and 1,25(OH)(2)D (beta = -.07/10%, P < .001) were independently associated with lower CortBMD Z-scores at baseline. The correlations of total, free, and bioavailable 25(OH)D with CortBMD did not differ. Higher baseline 1,25(OH)(2)D (P < .05) and greater increases in PTH (P < .001) were associated with greater declines in CortBMD Z-scores. Greater increases in calcium concentrations were associated with greater increases in CortBMD Z-scores in growing children (interaction P = .009). The hazard ratio for fracture was 1.75 (95% confidence interval 1.15-2.67; P = .009) per SD lower baseline CortBMD. Conclusions: Greater PTH and 1,25(OH)(2)D and lower calcium concentrations were independently associated with baseline and progressive cortical deficits in childhood CKD. Lower CortBMD Z-score was associated with increased fracture risk. (J Clin Endocrinol Metab 98: 1930-1938, 2013)

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