Report
Pilot study of vitamin D supplementation in adults with cystic fibrosis pulmonary exacerbation: A randomized, controlled trial
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Volume 4, Issue 2 April/May/June 2012
Pages 191 - 197
http://dx.doi.org/10.4161/derm.20332
Keywords: anti-microbial peptide, cystic fibrosis, parathyroid hormone, pulmonary exacerbation, vitamin D
Authors: Ruth E. Grossmann, Susu M. Zughaier, Meena Kumari, Shabnam Seydafkan, Robert H. Lyles, Shuling Liu, Viranuj Sueblinvong, Michael S. Schechter, Arlene A. Stecenko, Thomas R. Ziegler and Vin Tangpricha
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- Ruth E. Grossmann
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Nutrition Health Sciences Program; Emory Graduate Division of Biological and Biomedical Sciences; Emory University; Atlanta, GA USA
- Susu M. Zughaier
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Division of Pulmonology, Allergy/Immunology, Cystic Fibrosis and Sleep; Department of Pediatrics; Emory University School of Medicine; Atlanta, GA USA; Center for Cystic Fibrosis Research; Children’s Healthcare of Atlanta; Atlanta, GA USA
- Meena Kumari
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Division of Endocrinology, Metabolism and Lipids; Department of Medicine; Emory University School of Medicine; Atlanta, GA USA
- Shabnam Seydafkan
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Division of Endocrinology, Metabolism and Lipids; Department of Medicine; Emory University School of Medicine; Atlanta, GA USA
- Robert H. Lyles
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Department of Biostatistics and Bioinformatics; Rollins School of Public Health; Emory University; Atlanta, GA USA
- Shuling Liu
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Department of Biostatistics and Bioinformatics; Rollins School of Public Health; Emory University; Atlanta, GA USA
- Viranuj Sueblinvong
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Division of Pulmonary, Allergy, Critical Care and Sleep Medicine; Department of Medicine; Emory University School of Medicine; Atlanta, GA USA; Center for Cystic Fibrosis Research; Children’s Healthcare of Atlanta; Atlanta, GA USA
- Michael S. Schechter
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Division of Pulmonology, Allergy/Immunology, Cystic Fibrosis and Sleep; Department of Pediatrics; Emory University School of Medicine; Atlanta, GA USA; Children’s Healthcare of Atlanta; Atlanta, GA USA; Center for Cystic Fibrosis Research; Children’s Healthcare of Atlanta; Atlanta, GA USA
- Arlene A. Stecenko
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Division of Pulmonology, Allergy/Immunology, Cystic Fibrosis and Sleep; Department of Pediatrics; Emory University School of Medicine; Atlanta, GA USA; Center for Cystic Fibrosis Research; Children’s Healthcare of Atlanta; Atlanta, GA USA
- Thomas R. Ziegler
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Nutrition Health Sciences Program; Emory Graduate Division of Biological and Biomedical Sciences; Emory University; Atlanta, GA USA; Division of Endocrinology, Metabolism and Lipids; Department of Medicine; Emory University School of Medicine; Atlanta, GA USA
- Vin Tangpricha
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Corresponding author: vin.tangpricha@emory.edu
Nutrition Health Sciences Program; Emory Graduate Division of Biological and Biomedical Sciences; Emory University; Atlanta, GA USA; Division of Endocrinology, Metabolism and Lipids; Department of Medicine; Emory University School of Medicine; Atlanta, GA USA; Staff Physician; Atlanta VA Medical Center; Atlanta, GA USA; Center for Cystic Fibrosis Research; Children’s Healthcare of Atlanta; Atlanta, GA USA
Abstract:
Background: Vitamin D insufficiency is common in cystic fibrosis (CF) and vitamin D repletion may have an important role in improving clinical outcomes in CF. This randomized, placebo-controlled, pilot study examined the feasibility and impact of a single, large dose of cholecalciferol on vitamin D status and clinical outcomes in subjects with CF.
Methods: Thirty adults with were randomized in a double-blinded, pilot study to receive 250,000 IU cholecalciferol or placebo within 48 h of hospital admission for a pulmonary exacerbation. Concentrations of 25-hydroxyvitamin D (25(OH)D), clinical outcomes and potential adverse events were assessed up to one year after randomization. Mixed effects linear regression models were used to evaluate the difference in mean serum concentrations and log-rank analyses were used to evaluate survival.
Results: Data from all subjects was analyzed. Serum 25(OH)D concentrations increased from a mean of 30.6 ± 3.2 ng/mL to 58.1 ± 3.5 ng/mL (p < 0.001) at one week and 36.7 ± 2.6 ng/mL by 12 weeks (p = 0.06) in the vitamin D group; in contrast, serum 25(OH)D concentrations remained unchanged in the placebo group. Unadjusted, one-year survival and hospital-free days were increased in the vitamin D group (p = 0.029, p = 0.036; respectively). There was also a trend toward increased IV antibiotic therapy-free days in the vitamin D group (p = 0.073). There were no signs of hypervitaminosis D or adverse events. Serum PTH and calcium concentrations were similar across both groups.
Conclusions: In this pilot study, a single, oral bolus of cholecalciferol increased serum 25(OH)D concentrations and was associated with a trend toward improved clinical outcomes in CF subjects hospitalized for a pulmonary exacerbation. Further investigation is needed into the clinical impact of improved vitamin D status in patients with CF.
Received: February 16, 2012; Accepted: April 10, 2012
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