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Vitamin D for the Immune System in Cystic Fibrosis (DISC): a double-blind, multicenter, randomized, placebo-controlled clinical trial.

Authors :
Tangpricha, Vin
Lukemire, Joshua
Chen, Yuqing
Binongo, José Nilo G
Judd, Suzanne E
Michalski, Ellen S
Lee, Moon J
Walker, Seth
Ziegler, Thomas R
Tirouvanziam, Rabin
Zughaier, Susu M
Chesdachai, Supavit
Hermes, Wendy A
Chmiel, James F
Grossmann, Ruth E
Gaggar, Amit
Joseph, Patricia M
Alvarez, Jessica A
Source :
American Journal of Clinical Nutrition; Mar2019, Vol. 109 Issue 3, p544-553, 10p, 1 Diagram, 3 Charts, 3 Graphs
Publication Year :
2019

Abstract

Background Patients with cystic fibrosis (CF) have increased risk of vitamin D deficiency owing to fat malabsorption and other factors. Vitamin D deficiency has been associated with increased risk of pulmonary exacerbations of CF. Objectives The primary objective of this study was to examine the impact of a single high-dose bolus of vitamin D<subscript>3</subscript> followed by maintenance treatment given to adults with CF during an acute pulmonary exacerbation on future recurrence of pulmonary exacerbations. Methods This was a multicenter, double-blind, placebo-controlled, intent-to-treat clinical trial. Subjects with CF were randomly assigned to oral vitamin D<subscript>3</subscript> given as a single dose of 250,000 International Units (IU) or to placebo within 72 h of hospital admission for an acute pulmonary exacerbation, followed by 50,000 IU of vitamin D<subscript>3</subscript> or an identically matched placebo pill taken orally every other week starting at 3 mo after random assignment. The primary outcome was the composite endpoint of the time to next pulmonary exacerbation or death within 1 y. The secondary outcomes included circulating concentrations of the antimicrobial peptide cathelicidin and recovery of lung function as assessed by the percentage of predicted forced expiratory volume in 1 s (FEV1%). Results A total of 91 subjects were enrolled in the study. There were no differences between the vitamin D<subscript>3</subscript> and placebo groups in time to next pulmonary exacerbation or death at 1 y. In addition, there were no differences in serial recovery of lung function after pulmonary exacerbation by FEV1% or in serial concentrations of plasma cathelicidin. Conclusions Vitamin D<subscript>3</subscript> initially given at the time of pulmonary exacerbation of CF did not alter the time to the next pulmonary exacerbation, 12-mo mortality, serial lung function, or serial plasma cathelicidin concentrations. This trial was registered at clinicaltrials.gov as NCT01426256. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00029165
Volume :
109
Issue :
3
Database :
Complementary Index
Journal :
American Journal of Clinical Nutrition
Publication Type :
Academic Journal
Accession number :
135517637
Full Text :
https://doi.org/10.1093/ajcn/nqy291