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Transient receptor potential vanilloid 1 (TRPV1) antagonism in patients with refractory chronic cough: A double-blind randomized controlled trial - 27/06/14

Doi : 10.1016/j.jaci.2014.01.038 
Saifudin Khalid, MB BS, PhD a, Robert Murdoch, BSc, PhD b, Amy Newlands, BSc, MSc b, Kevin Smart, BSc, PhD b, Angela Kelsall, BSc, PhD a, Kimberley Holt, BSc a, Rachel Dockry, BSc, MSc a, Ashley Woodcock, MB ChB, MD a, Jaclyn A. Smith, MB ChB, PhD a,
a Centre for Respiratory and Allergy, University of Manchester, University Hospital of South Manchester, Manchester, United Kingdom 
b GlaxoSmithKline, Stevenage, United Kingdom 

Corresponding author: Jaclyn A. Smith, MB ChB, PhD, Education and Research Centre, 2nd Floor, University Hospital of South Manchester, Southmoor Rd, Manchester, M23 9LT, United Kingdom.

Abstract

Background

Inhalation of capsaicin, the extract of hot chili peppers, induces coughing in both animals and human subjects through activation of transient receptor potential vanilloid 1 (TRPV1) on airway sensory nerves. Therefore the TRPV1 receptor is an attractive target for the development of antitussive agents.

Objective

We sought to assess the antitussive effect of TRPV1 antagonism in patients with refractory chronic cough.

Methods

Twenty-one subjects with refractory chronic cough (>8 weeks) attending a specialist clinic were recruited to a randomized, double-blind, placebo-controlled crossover trial assessing a TRPV1 antagonist (SB-705498). Cough reflex sensitivity to capsaicin (concentration of capsaicin inducing at least 5 coughs) and 24-hour cough frequency were coprimary end points assessed after a single dose of SB-705498 (600 mg) and matched placebo. Cough severity and urge to cough were reported on visual analog scales, and cough-specific quality of life data were also collected.

Results

Treatment with SB-705498 produced a significant improvement in cough reflex sensitivity to capsaicin at 2 hours and a borderline significant improvement at 24 hours compared with placebo (adjusted mean difference of +1.3 doubling doses at 2 hours [95% CI, +0.3 to +2.2; P = .0049] and +0.7 doubling doses at 24 hours [95% CI, +0.0 to +1.5; P = .0259]). However, 24-hour objective cough frequency was not improved compared with placebo. Patient-reported cough severity, urge to cough, and cough-specific quality of life similarly suggested no effect of SB-705498.

Conclusion

This study raises important questions about both the role of TRVP1-mediated mechanisms in patients with refractory chronic cough and also the predictive value of capsaicin challenge testing in the assessment of novel antitussive agents.

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Key words : Cough, transient receptor potential vanilloid 1, capsaicin, cough sounds, sensory nerves

Abbreviations used : C2, C5, CQLQ, HRT, IQR, Tmax, TRPV1, VAS


Plan


 Supported by GlaxoSmithKline. J.A.S. was funded by an MRC Clinician Scientist award (G0701918).
 Disclosure of potential conflict of interest: R. Murdoch and A. Newlands are employed by and have stock holdings in GlaxoSmithKline. A. Woodcock has received research support from GlaxoSmithKline, Afferent, and Verona; has received consultancy fees from Merck; and has a patent on ambulatory cough monitor owned by University Hospital of South Manchester. J. A. Smith has received research support from GlaxoSmithKline, AstraZeneca, and Afferent; has received consulting fees from Almirall, GlaxoSmithKline, Xention, Glenmark, Theravance, Novartis, and Reckitt and Benckiser; and has a patent owned by the University Hospital South Manchester for describing methods for detecting cough from sound. The rest of the authors declare they have no relevant conflicts of interest.


© 2014  American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 134 - N° 1

P. 56 - juillet 2014 Retour au numéro
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