4.4 Article

Prevalence and correlates of 25-hydroxyvitamin D deficiency in the Chronic Kidney Disease in Children (CKiD) cohort

Journal

PEDIATRIC NEPHROLOGY
Volume 31, Issue 1, Pages 121-129

Publisher

SPRINGER
DOI: 10.1007/s00467-015-3190-7

Keywords

Mineral metabolism; Pediatric; Chronic renal disease; Hyperparathyroidism; Fibroblast growth factor 23

Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases
  2. Eunice Kennedy Shriver National Institute of Child Health and Human Development
  3. National Heart, Lung, and Blood Institute [U01-DK66143, U01-DK66174, U01-DK82194, U01-DK66116]

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Vitamin D plays an important role in the mineral and bone disorder seen in chronic kidney disease (CKD). Deficiency of 25-hydroxyvitamin D (25OHD) is highly prevalent in the adult CKD population. The prevalence and determinants of 25OHD deficiency (defined as a level < 20 ng/ml) were examined longitudinally in 506 children in the CKiD cohort. Predictors of secondary hyperparathyroidism and the determinants of 1,25-dihydroxyvitamin D (1,25(OH)(2)D) levels were also evaluated. Deficiency of 25OHD was observed in 28 % of the cohort at enrollment. Significant predictors of 25OHD deficiency were older age, non-white race, higher body mass index, assessment during winter, less often than daily milk intake, non-use of nutritional vitamin D supplement and proteinuria. Lower values of glomerular filtration rate (GFR), serum 25OHD, calcium and higher levels of FGF23 were significant determinants of secondary hyperparathyroidism. Lower GFR, low serum 25OHD, nephrotic-range proteinuria, and high FGF23 levels were significant determinants of serum 1,25(OH)(2) D levels. Deficiency of 25OHD is prevalent in children with CKD and is associated with potentially modifiable risk factors such as milk intake, nutritional vitamin D supplement use, and proteinuria. 25OHD deficiency is a risk factor for secondary hyperparathyroidism and decreased serum 1,25(OH)(2)D in children with CKD.

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