Critically ill children have low Vitamin D-binding protein, influencing bioavailability of Vitamin D

Kate Madden, Henry A. Feldman, Rene F. Chun, Ellen M. Smith, Ryan M. Sullivan, Anna A. Agan, Shannon M. Keisling, Angela Panoskaltsis-Mortari, Adrienne G. Randolph

Research output: Contribution to journalArticle

24 Scopus citations

Abstract

Rationale: Vitamin D deficiency, often defined by total serum 25-hydroxyvitamin D (25[OH]D) <20 ng/ml, is common in critically ill patients, with associations with increasedmortality andmorbidity in the intensive care unit. Correction of vitamin D deficiency in critical illness has been recommended, and ongoing clinical trials are investigating the effect of repletion on patient outcome. The biologically active amount of 25(OH)D depends on the concentration and protein isoformof vitamin D-binding protein (VDBP), which is also an acutephase reactant affected by inflammation and injury. Objectives: We performed a secondary analysis of a cohort of critically ill children in which we reported a high rate of vitamin D deficiency, to examine how VDBP level and genotype would impact vitamin D status. Methods: We prospectively enrolled 511 children admitted to the pediatric intensive care unit over a 12-month period. Measurements and Main Results: We measured serum VDBP in 479 children. We genotyped single nucleotide polymorphisms rs7041 and rs4588 in the VDBP gene (GC) to determine haplotypes GC1F, GC1S, and GC2 in 178 subjects who consented, then calculated bioavailable 25(OH)D from serum 25(OH)D, VDBP, albumin, and GC haplotype. The median serum VDBP level was 159 mg/ml (interquartile range, 108-221), lower than has been reported in healthy children. Factors predicting lower levels in multivariate analysis included age <1 year, nonwhite race, being previously healthy, 25(OH)D<20 ng/ml and greater illness severity. In the subgroup that was genotyped, GC haplotype had the strongest association with VDBP level; carriage of one additional copy of GC1S was associated with a 37.5% higher level (95% confidence interval, 31.9-44.8; P <0.001). Bioavailable 25(OH)D was also inversely associated with illness severity (r = 20.24, P <0.001), and ratio to measured total 25(OH)D was variable and related to haplotype. Conclusions: Physiologic deficiency of 25(OH)D in critical illness may be more difficult to diagnose, given that lower VDBP levels increase bioavailability. Treatment studies conducted on the basis of total 25(OH)D level, without consideration of VDBP concentration and genotype, may increase the risk of falsely negative results.

Original languageEnglish (US)
Pages (from-to)1654-1661
Number of pages8
JournalAnnals of the American Thoracic Society
Volume12
Issue number11
DOIs
StatePublished - Nov 2015

Keywords

  • Bioavailability
  • Critical illness
  • Haplotype
  • Vitamin D
  • Vitamin D-binding protein

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    Madden, K., Feldman, H. A., Chun, R. F., Smith, E. M., Sullivan, R. M., Agan, A. A., Keisling, S. M., Panoskaltsis-Mortari, A., & Randolph, A. G. (2015). Critically ill children have low Vitamin D-binding protein, influencing bioavailability of Vitamin D. Annals of the American Thoracic Society, 12(11), 1654-1661. https://doi.org/10.1513/AnnalsATS.201503-160OC