Hyperglycemia and cystic fibrosis alter respiratory fluid glucose concentrations estimated by breath condensate analysis

1 Divisions of Cardiac and Vascular and Basic Medical Sciences, St. George's, University of London, London; 2 School of Human and Life Sciences, Whitelands College, Roehampton University, London; and 3 Department of Cystic Fibrosis, Royal Brompton Hospital, London, United Kingdom Submitted 15 D...

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Bibliographic Details
Published in:Journal of applied physiology (1985) 2007-05, Vol.102 (5), p.1969-1975
Main Authors: Baker, Emma H, Clark, Nicholas, Brennan, Amanda L, Fisher, Donald A, Gyi, Khin M, Hodson, Margaret E, Philips, Barbara J, Baines, Deborah L, Wood, David M
Format: Article
Language:English
Subjects:
Adult
Anion Exchange Resins
Biological and medical sciences
Blood Glucose - metabolism
Body fluids
Breath Tests - methods
Chromatography, Ion Exchange - methods
Cystic fibrosis
Cystic Fibrosis - blood
Cystic Fibrosis - metabolism
Cystic Fibrosis - physiopathology
Diabetes
Diabetes Mellitus - blood
Diabetes Mellitus - metabolism
Diabetes Mellitus - physiopathology
Exhalation
Female
Fundamental and applied biological sciences. Psychology
Glucose
Glucose - metabolism
Glucose Tolerance Test
Humans
Hyperglycemia
Hyperglycemia - blood
Hyperglycemia - metabolism
Hyperglycemia - physiopathology
London
Male
Reproducibility of Results
Respiratory diseases
Saliva - metabolism
Sensitivity and Specificity
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Summary:1 Divisions of Cardiac and Vascular and Basic Medical Sciences, St. George's, University of London, London; 2 School of Human and Life Sciences, Whitelands College, Roehampton University, London; and 3 Department of Cystic Fibrosis, Royal Brompton Hospital, London, United Kingdom Submitted 15 December 2006 ; accepted in final form 12 February 2007 In animals, glucose concentrations are 3–20 times lower in lung lining fluid than in plasma. In humans, glucose concentrations are normally low (
ISSN:8750-7587
1522-1601
DOI:10.1152/japplphysiol.01425.2006