Literature DB >> 30969149

Multiprobe Nuclear Imaging of the Cystic Fibrosis Lung as a Biomarker of Therapeutic Effect.

Timothy E Corcoran1,2,3, Alex S Huber2, Michael M Myerburg1, Daniel J Weiner4, Landon W Locke5, Ryan T Lacy3, Lawrence Weber6, Michael R Czachowski6, Darragh J Johnston2, Ashok Muthukrishnan7, Alison T Lennox1, Joseph M Pilewski1,4,8.   

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.

Entities:  

Keywords:  CFTR; DTPA; airway surface liquid; mucociliary clearance

Mesh:

Substances:

Year:  2019        PMID: 30969149      PMCID: PMC6685188          DOI: 10.1089/jamp.2018.1491

Source DB:  PubMed          Journal:  J Aerosol Med Pulm Drug Deliv        ISSN: 1941-2711            Impact factor:   2.849


  15 in total

1.  Overnight delivery of hypertonic saline by nasal cannula aerosol for cystic fibrosis.

Authors:  Timothy E Corcoran; Joseph E Godovchik; Karl H Donn; David R Busick; Jennifer Goralski; Landon W Locke; Matthew R Markovetz; Michael M Myerburg; Ashok Muthukrishnan; Lawrence Weber; Ryan T Lacy; Joseph M Pilewski
Journal:  Pediatr Pulmonol       Date:  2017-07-24

2.  Effect of Posture on Regional Deposition of Coarse Particles in the Healthy Human Lung.

Authors:  Rui Carlos Sá; Kirby L Zeman; William D Bennett; G Kim Prisk; Chantal Darquenne
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2015-03-31       Impact factor: 2.849

3.  The effect of inhaled mannitol on bronchial mucus clearance in cystic fibrosis patients: a pilot study.

Authors:  M Robinson; E Daviskas; S Eberl; J Baker; H K Chan; S D Anderson; P T Bye
Journal:  Eur Respir J       Date:  1999-09       Impact factor: 16.671

4.  Clinical mechanism of the cystic fibrosis transmembrane conductance regulator potentiator ivacaftor in G551D-mediated cystic fibrosis.

Authors:  Steven M Rowe; Sonya L Heltshe; Tanja Gonska; Scott H Donaldson; Drucy Borowitz; Daniel Gelfond; Scott D Sagel; Umer Khan; Nicole Mayer-Hamblett; Jill M Van Dalfsen; Elizabeth Joseloff; Bonnie W Ramsey
Journal:  Am J Respir Crit Care Med       Date:  2014-07-15       Impact factor: 21.405

5.  Mucus clearance and lung function in cystic fibrosis with hypertonic saline.

Authors:  Scott H Donaldson; William D Bennett; Kirby L Zeman; Michael R Knowles; Robert Tarran; Richard C Boucher
Journal:  N Engl J Med       Date:  2006-01-19       Impact factor: 91.245

6.  Quantitative imaging of airway liquid absorption in cystic fibrosis.

Authors:  Landon W Locke; Michael M Myerburg; Matthew R Markovetz; Robert S Parker; Lawrence Weber; Michael R Czachowski; Thomas J Harding; Stefanie L Brown; Joseph A Nero; Joseph M Pilewski; Timothy E Corcoran
Journal:  Eur Respir J       Date:  2014-04-17       Impact factor: 16.671

7.  Phenazine content in the cystic fibrosis respiratory tract negatively correlates with lung function and microbial complexity.

Authors:  Ryan C Hunter; Vanja Klepac-Ceraj; Magen M Lorenzi; Hannah Grotzinger; Thomas R Martin; Dianne K Newman
Journal:  Am J Respir Cell Mol Biol       Date:  2012-08-03       Impact factor: 6.914

8.  Mucus removal is impaired in children with cystic fibrosis who have been infected by Pseudomonas aeruginosa.

Authors:  Beth L Laube; Gail Sharpless; Jane Benson; Kathryn A Carson; Peter J Mogayzel
Journal:  J Pediatr       Date:  2013-12-24       Impact factor: 4.406

9.  Liquid hyper-absorption as a cause of increased DTPA clearance in the cystic fibrosis airway.

Authors:  Timothy E Corcoran; Kristina M Thomas; Stefanie Brown; Michael M Myerburg; Landon W Locke; Joseph M Pilewski
Journal:  EJNMMI Res       Date:  2013-02-27       Impact factor: 3.138

10.  Sweat chloride as a biomarker of CFTR activity: proof of concept and ivacaftor clinical trial data.

Authors:  Frank J Accurso; Fredrick Van Goor; Jiuhong Zha; Anne J Stone; Qunming Dong; Claudia L Ordonez; Steven M Rowe; John Paul Clancy; Michael W Konstan; Heather E Hoch; Sonya L Heltshe; Bonnie W Ramsey; Preston W Campbell; Melissa A Ashlock
Journal:  J Cyst Fibros       Date:  2014-03       Impact factor: 5.527

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  3 in total

1.  A physiologically-motivated model of cystic fibrosis liquid and solute transport dynamics across primary human nasal epithelia.

Authors:  Florencio Serrano Castillo; Carol A Bertrand; Michael M Myerburg; Monica E Shapiro; Timothy E Corcoran; Robert S Parker
Journal:  J Pharmacokinet Pharmacodyn       Date:  2019-09-07       Impact factor: 2.745

Review 2.  Mucus, mucins, and cystic fibrosis.

Authors:  Cameron Bradley Morrison; Matthew Raymond Markovetz; Camille Ehre
Journal:  Pediatr Pulmonol       Date:  2019-11

3.  Mucociliary Clearance Differs in Mild Asthma by Levels of Type 2 Inflammation.

Authors:  Timothy E Corcoran; Alex S Huber; Sherri L Hill; Landon W Locke; Lawrence Weber; Ashok Muthukrishnan; Elisa M Heidrich; Sally Wenzel; Mike M Myerburg
Journal:  Chest       Date:  2021-05-21       Impact factor: 9.410

  3 in total

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