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المؤلفTangpricha V.
المؤلفLukemire J.
المؤلفChen Y.
المؤلفBinongo J.N.G.
المؤلفJudd S.E.
المؤلفMichalski E.S.
المؤلفLee M.J.
المؤلفWalker S.
المؤلفZiegler T.R.
المؤلفTirouvanziam R.
المؤلفZughaier S.M.
المؤلفChesdachai S.
المؤلفHermes W.A.
المؤلفChmiel J.F.
المؤلفGrossmann R.E.
المؤلفGaggar A.
المؤلفJoseph P.M.
المؤلفAlvarez J.A.
تاريخ الإتاحة2020-04-25T01:02:19Z
تاريخ النشر2019
اسم المنشورAmerican Journal of Clinical Nutrition
المصدرScopus
الرقم المعياري الدولي للكتاب29165
معرّف المصادر الموحدhttp://dx.doi.org/10.1093/ajcn/nqy291
معرّف المصادر الموحدhttp://hdl.handle.net/10576/14423
الملخصBackground 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 3 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 3 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 3 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 3 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 3 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.
راعي المشروعSupported by Cystic Fibrosis Foundation grants TANGPR11A0 (to VT) and JOSEPH15YO (to PMJ) and NIH grants UL1 TR000454 (Emory CTSA), UL1 TR000165 (UAB CTSA), T32 DK007298 (to JAA), T32 DK007734 (to ESM), K24 DK096574 (to TRZ), and K01 DK102851 (to JAA).
اللغةen
الناشرOxford University Press
الموضوعcathelicidin
clinical trial
cystic fibrosis
lung function
nutrition
pulmonary exacerbation
Vitamin D
العنوانVitamin D for the Immune System in Cystic Fibrosis (DISC): A double-blind, multicenter, randomized, placebo-controlled clinical trial
النوعArticle
الصفحات554-565
رقم العدد3
رقم المجلد109


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