Literature DB >> 24332997

Iron supplementation does not worsen respiratory health or alter the sputum microbiome in cystic fibrosis.

Alex H Gifford1, Diana M Alexandru2, Zhigang Li3, Dana B Dorman4, Lisa A Moulton5, Katherine E Price6, Thomas H Hampton7, Mitchell L Sogin8, Jonathan B Zuckerman9, H Worth Parker10, Bruce A Stanton11, George A O'Toole12.   

Abstract

BACKGROUND: Iron supplementation for hypoferremic anemia could potentiate bacterial growth in the cystic fibrosis (CF) lung, but clinical trials testing this hypothesis are lacking.
METHODS: Twenty-two adults with CF and hypoferremic anemia participated in a randomized, double-blind, placebo-controlled, crossover trial of ferrous sulfate 325mg daily for 6weeks. Iron-related hematologic parameters, anthropometric data, sputum iron, Akron Pulmonary Exacerbation Score (PES), and the sputum microbiome were serially assessed. Fixed-effect models were used to describe how ferrous sulfate affected these variables.
RESULTS: Ferrous sulfate increased serum iron by 22.3% and transferrin saturation (TSAT) by 26.8% from baseline (p<0.05) but did not affect hemoglobin, sputum iron, Akron PES, and the sputum microbiome.
CONCLUSIONS: Low-dose ferrous sulfate improved hypoferremia without correcting anemia after 6weeks. We did not observe significant effects on sputum iron, Akron PES, and the sputum microbiome. Although we did not identify untoward health effects of iron supplementation, a larger blinded randomized controlled trial would be needed to fully demonstrate safety.
Copyright © 2013 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Anemia; Cystic fibrosis; Hepcidin-25; Hypoferremia; Iron; Microbiome

Mesh:

Substances:

Year:  2013        PMID: 24332997      PMCID: PMC3972336          DOI: 10.1016/j.jcf.2013.11.004

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  42 in total

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Review 3.  Iron homeostasis and erythropoiesis.

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4.  The DeltaF508-CFTR mutation results in increased biofilm formation by Pseudomonas aeruginosa by increasing iron availability.

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6.  Immunoassay for human serum hepcidin.

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Review 7.  Iron acquisition by Pseudomonas aeruginosa in the lungs of patients with cystic fibrosis.

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  18 in total

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Review 3.  Cystic Fibrosis Airway Microbiome: Overturning the Old, Opening the Way for the New.

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Review 4.  Nutritional immunity: the impact of metals on lung immune cells and the airway microbiome during chronic respiratory disease.

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7.  Availability of Zinc Impacts Interactions between Streptococcus sanguinis and Pseudomonas aeruginosa in Coculture.

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9.  Serum Iron Level Is Associated with Time to Antibiotics in Cystic Fibrosis.

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