Vitamin D deficiency is associated with pulmonary dysfunction in cystic fibrosis

William P. Sexauer, Anas Hadeh, Pamela A. Ohman-Strickland, Robert L. Zanni, Laurie Varlotta, Douglas Holsclaw, Stanley Fiel, Gavin R. Graff, Arthur Atlas, Dorothy Bisberg, Denis Hadjiliadis, Suzanne H. Michel, Daria Mintz, Rebanta Chakraborty, Bridget Marra, Paula Lomas, Tara Ward, Meagen Sassman, Giovanna C. Imbesi, Diane M. KitchAllison M. Mallowe

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

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±12.8ng/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.

Original languageEnglish (US)
Pages (from-to)497-506
Number of pages10
JournalJournal of Cystic Fibrosis
Volume14
Issue number4
DOIs
StatePublished - Jul 1 2015

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Pulmonary and Respiratory Medicine

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