Vitamin D deficiency is associated with pulmonary dysfunction in cystic fibrosis

J Cyst Fibros. 2015 Jul;14(4):497-506. doi: 10.1016/j.jcf.2014.12.006. Epub 2015 Jan 7.

Abstract

Background: Vitamin D deficiency is common in CF. Whether vitamin D affects pulmonary function in CF is unknown.

Methods: Data were abstracted from clinically stable CF patients who had pulmonary function studies and serum 25-hydroxyvitamin D [25(OH)D, ng/ml] levels drawn within 2 months of each other. Findings were adjusted for multiple variables known to affect pulmonary function in CF.

Results: Enrollees totaled 597. Overall mean 25(OH)D level was 29.6±12.8 ng/ml (SD). Serum 25(OH)D levels showed a significant correlation with forced expiratory volume in 1s (FEV1) % predicted (r=0.20, p<0.0001) and forced vital capacity % predicted (r=0.13, p=0.0019). Multivariate analysis revealed that serum 25(OH)D remained an independent predictor of FEV1 % predicted even after controlling for multiple other factors known to affect CF lung function.

Conclusions: Serum 25(OH)D levels are significantly associated with pulmonary function in CF. Further study is required to determine whether this association is causal.

Keywords: Cystic fibrosis; Lung function; Pulmonary function; Vitamin D.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Cystic Fibrosis / blood
  • Cystic Fibrosis / complications*
  • Cystic Fibrosis / physiopathology*
  • Female
  • Forced Expiratory Volume / physiology
  • Humans
  • Male
  • Retrospective Studies
  • Vital Capacity / physiology
  • Vitamin D / analogs & derivatives
  • Vitamin D / blood
  • Vitamin D Deficiency / blood
  • Vitamin D Deficiency / complications*
  • Vitamin D Deficiency / physiopathology*
  • Young Adult

Substances

  • Vitamin D
  • 25-hydroxyvitamin D