Literature DB >> 27115955

Hydrator Therapies for Chronic Bronchitis. Lessons from Cystic Fibrosis.

William D Bennett1,2,3, Ashley G Henderson1,2, Scott H Donaldson1,2.   

Abstract

Patients with the chronic bronchitis form of chronic obstructive pulmonary disease and cystic fibrosis share similar clinical features, including mucus obstruction of airways and the development of chronic/recurrent airways infections that often manifest as disease exacerbations. There is growing evidence that these diseases may have parallels in disease pathogenesis as well, including cystic fibrosis transmembrane conductance regulator dysfunction, mucus dehydration, and defective mucociliary clearance. As progress is made in the development of therapies that target the basic defects that lead to cystic fibrosis lung disease, it is possible that similar approaches could also benefit patients with chronic bronchitis. A deeper understanding of how tobacco smoke and other triggers of chronic bronchitis actually lead to disease, and exploration of the concept that therapies that restore cystic fibrosis transmembrane conductance regulator function, mucus hydration, and/or mucociliary clearance may benefit patients with chronic bronchitis, hold the prospect of significant progress in treating this prevalent disease.

Entities:  

Keywords:  bronchitis; chronic obstructive pulmonary disease; hydrator; hypertonic saline; mucociliary clearance

Mesh:

Substances:

Year:  2016        PMID: 27115955      PMCID: PMC5015724          DOI: 10.1513/AnnalsATS.201509-652KV

Source DB:  PubMed          Journal:  Ann Am Thorac Soc        ISSN: 2325-6621


  38 in total

1.  The Relationship of Mucus Concentration (Hydration) to Mucus Osmotic Pressure and Transport in Chronic Bronchitis.

Authors:  Wayne H Anderson; Raymond D Coakley; Brian Button; Ashley G Henderson; Kirby L Zeman; Neil E Alexis; David B Peden; Eduardo R Lazarowski; C William Davis; Summer Bailey; Fred Fuller; Martha Almond; Bahjat Qaqish; Elena Bordonali; Michael Rubinstein; William D Bennett; Mehmet Kesimer; Richard C Boucher
Journal:  Am J Respir Crit Care Med       Date:  2015-07-15       Impact factor: 21.405

Review 2.  Airway surface dehydration in cystic fibrosis: pathogenesis and therapy.

Authors:  Richard C Boucher
Journal:  Annu Rev Med       Date:  2007       Impact factor: 13.739

3.  Inhalation of dry powder mannitol improves clearance of mucus in patients with bronchiectasis.

Authors:  E Daviskas; S D Anderson; S Eberl; H K Chan; G Bautovich
Journal:  Am J Respir Crit Care Med       Date:  1999-06       Impact factor: 21.405

4.  Rheology of cystic fibrosis sputum after in vitro treatment with hypertonic saline alone and in combination with recombinant human deoxyribonuclease I.

Authors:  M King; B Dasgupta; R P Tomkiewicz; N E Brown
Journal:  Am J Respir Crit Care Med       Date:  1997-07       Impact factor: 21.405

5.  Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.

Authors:  Claire E Wainwright; J Stuart Elborn; Bonnie W Ramsey; Gautham Marigowda; Xiaohong Huang; Marco Cipolli; Carla Colombo; Jane C Davies; Kris De Boeck; Patrick A Flume; Michael W Konstan; Susanna A McColley; Karen McCoy; Edward F McKone; Anne Munck; Felix Ratjen; Steven M Rowe; David Waltz; Michael P Boyle
Journal:  N Engl J Med       Date:  2015-05-17       Impact factor: 91.245

6.  Some gating potentiators, including VX-770, diminish ΔF508-CFTR functional expression.

Authors:  Guido Veit; Radu G Avramescu; Doranda Perdomo; Puay-Wah Phuan; Miklos Bagdany; Pirjo M Apaja; Florence Borot; Daniel Szollosi; Yu-Sheng Wu; Walter E Finkbeiner; Tamas Hegedus; Alan S Verkman; Gergely L Lukacs
Journal:  Sci Transl Med       Date:  2014-07-23       Impact factor: 17.956

7.  Long-term cigarette smoke exposure in a mouse model of ciliated epithelial cell function.

Authors:  Samantha M Simet; Joseph H Sisson; Jacqueline A Pavlik; Jane M Devasure; Craig Boyer; Xiangde Liu; Shin Kawasaki; John G Sharp; Stephen I Rennard; Todd A Wyatt
Journal:  Am J Respir Cell Mol Biol       Date:  2009-12-30       Impact factor: 6.914

8.  Enhanced clearance of secretions from the human lung after the administration of hypertonic saline aerosol.

Authors:  D Pavia; M L Thomson; S W Clarke
Journal:  Am Rev Respir Dis       Date:  1978-02

9.  Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.

Authors:  David A Stoltz; David K Meyerholz; Alejandro A Pezzulo; Shyam Ramachandran; Mark P Rogan; Greg J Davis; Robert A Hanfland; Chris Wohlford-Lenane; Cassie L Dohrn; Jennifer A Bartlett; George A Nelson; Eugene H Chang; Peter J Taft; Paula S Ludwig; Mira Estin; Emma E Hornick; Janice L Launspach; Melissa Samuel; Tatiana Rokhlina; Philip H Karp; Lynda S Ostedgaard; Aliye Uc; Timothy D Starner; Alexander R Horswill; Kim A Brogden; Randall S Prather; Sandra S Richter; Joel Shilyansky; Paul B McCray; Joseph Zabner; Michael J Welsh
Journal:  Sci Transl Med       Date:  2010-04-28       Impact factor: 17.956

10.  Acquired defects in CFTR-dependent β-adrenergic sweat secretion in chronic obstructive pulmonary disease.

Authors:  Clifford A Courville; Sherry Tidwell; Bo Liu; Frank J Accurso; Mark T Dransfield; Steven M Rowe
Journal:  Respir Res       Date:  2014-02-25
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  2 in total

1.  Effects of Different Inhalation Therapy on Ventilator-Associated Pneumonia in Ventilated COVID-19 Patients: A Randomized Controlled Trial.

Authors:  Nikola Delić; Andrija Matetic; Josipa Domjanović; Toni Kljaković-Gašpić; Lenko Šarić; Darko Ilić; Svjetlana Došenović; Josipa Domazet; Ruben Kovač; Frane Runjić; Sanda Stojanović Stipić; Božidar Duplančić
Journal:  Microorganisms       Date:  2022-05-28

Review 2.  Nebulized hypertonic saline in noncystic fibrosis bronchiectasis: a comprehensive review.

Authors:  Luis Máiz Carro; Miguel A Martínez-García
Journal:  Ther Adv Respir Dis       Date:  2019 Jan-Dec       Impact factor: 4.031

  2 in total

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