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Multiprobe Nuclear Imaging of the Cystic Fibrosis Lung as a Biomarker of Therapeutic Effect.
- Source :
-
Journal of aerosol medicine and pulmonary drug delivery [J Aerosol Med Pulm Drug Deliv] 2019 Aug; Vol. 32 (4), pp. 242-249. Date of Electronic Publication: 2019 Apr 10. - Publication Year :
- 2019
-
Abstract
- Background: Nuclear imaging biomarkers illustrate unique aspects of lung physiology and are useful for assessing therapeutic effects in cystic fibrosis (CF) lung disease. We have developed a multiprobe method to simultaneously measure mucociliary clearance (MCC) and paracellular absorption (ABS). MCC is a direct measure of mucus clearance. ABS has been related to airway surface liquid (ASL) absorption through previous in vitro studies. Methods: We describe baseline factors affecting MCC and ABS using data from a retrospective baseline group ( n = 22) and the response of the measures to inhaled 7% hypertonic saline (HS) and dry powder mannitol using data from a prospective response group ( n = 7). A retrospective healthy control group ( n = 15) is also described. The baseline and control groups performed single measurements of MCC/ABS. The response group performed baseline measurements of MCC/ABS and measurements after each intervention. Results: ABS was correlated (Spearman's ρ = 0.51, p = 0.06) to sweat chloride, a systemic measure of cystic fibrosis transmembrane conductance regulator (CFTR) function, whereas MCC was not. Baseline MCC was depressed after Pseudomonas aeruginosa infection as we have previously described. MCC provided a more sensitive indication of therapeutic effect and indicated improved clearance with mannitol compared with HS. Conclusion: MCC provides a useful and well-established means of testing therapies directed at improving mucus clearance in the lung. ABS may provide a means of detecting local changes in ASL absorption and CFTR function in the lung. Both are useful tools for studying the key aspects of CF lung pathophysiology (ASL hyperabsorption and MCC depression) that link the basic genetic defects of CF to disease manifestations in the lung.
- Subjects :
- Administration, Inhalation
Adolescent
Adult
Biomarkers metabolism
Case-Control Studies
Child
Cystic Fibrosis physiopathology
Cystic Fibrosis Transmembrane Conductance Regulator metabolism
Female
Humans
Lung physiopathology
Male
Mannitol administration & dosage
Prospective Studies
Retrospective Studies
Saline Solution, Hypertonic administration & dosage
Young Adult
Cystic Fibrosis diagnostic imaging
Lung diagnostic imaging
Mucociliary Clearance
Pseudomonas Infections diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 1941-2703
- Volume :
- 32
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Journal of aerosol medicine and pulmonary drug delivery
- Publication Type :
- Academic Journal
- Accession number :
- 30969149
- Full Text :
- https://doi.org/10.1089/jamp.2018.1491