TY - JOUR
T1 - A double-blind randomised placebo-controlled trial investigating the effects of lesogaberan on the objective cough frequency and capsaicin evoked coughs in patients with refractory chronic cough
AU - Badri, Huda
AU - Gibbard, Carmen
AU - Denton, Dimitra
AU - Satia, Imran
AU - Al-Sheklly, Bashar
AU - Dockry, Rachel J
AU - Holt, Kimberley
AU - McGuiness, Kevin
AU - Treadway, Sam
AU - Whorwell, Peter
AU - Houghton, Lesley
AU - Lee, Augustine
AU - Escott, K. Jane
AU - Lee, Theresa
AU - Wilkinson, Greame
AU - Holt, Alison
AU - Canning, Brendan J
AU - Smith, Jacky A
N1 - Funding Information:
Conflict of interest: J.A. Smith and K. McGuiness are inventors on a patent describing methods for detecting cough from sound recordings, licensed to Vitalograph Ltd. J.A. Smith has received funding for consultancy and research funds from Afferent Pharmaceuticals, Merck Inc., Bayer, Bellus, GSK, Xention Ltd, Ario Pharma Ltd, Glenmark, Almirall, AstraZeneca, Axalbion, Patara, Verona Pharma, NeRRe Pharmaceuticals, Menlo Pharmaceuticals and Attenua Inc. I. Satia reports grants from the ERS Respire 3 Marie Curie Fellowship, British Medical Association and North West Lung Centre Charity, grants and personal fees from Merck Canada, and personal fees from GSK and AstraZeneca, outside the submitted work. B.J. Canning is on the board of a pharmaceutical company. K.J. Escott is a current employee of AstraZeneca. G. Wilkinson and A. Holt are previous employees of AstraZeneca. H. Badri, C. Gibbard, D. Denton, B. Al-Sheklly, R.J. Dockry, K. Holt, S. Treadway, P. Whorwell, L. Houghton, A. Lee and T. Lee have no conflicts of interests.
Funding Information:
Support statement: This study was funded by an MRC “Mechanism of human disease” grant in collaboration with AstraZeneca MR/K015141/1. J.A. Smith is funded by the NIHR Manchester Biomedical Research Centre, a Wellcome Investigator in Science Award and is an NIHR Senior Investigator. H. Badri is funded by a North West Lung Centre Pickering Fellowship. I. Satia is currently supported by the E.J Moran Campbell Early Career Award, Dept of Medicine, McMaster University. Funding information for this article has been deposited with the Crossref Funder Registry.
Funding Information:
Acknowledgement: The delivery of this study was supported by the NIHR Manchester Clinical Research Facility.
Publisher Copyright:
© The authors 2022.
Copyright ©The authors 2022.
PY - 2022/3/2
Y1 - 2022/3/2
N2 - Objective Baclofen is a centrally acting γ-aminobutyric acid type B (GABA
B) receptor agonist which reduces gastro-oesophageal reflux and suppresses the cough reflex; however, central nervous system side-effects limit its use. Lesogaberan is a novel peripherally acting GABA
B agonist, but its effects on refractory chronic cough are unknown. Design We performed a single-centre, placebo-controlled, double-blind randomised crossover study in patients with chronic cough, refractory to the treatment of underlying conditions. Patients were randomised to treatment with lesogaberan 120 mg modified release twice daily or matched placebo for 2 weeks and then crossed over to the alternative therapy after a 2-week washout. The primary end-point was 24-h cough frequency measured with an acoustic monitoring system. In addition, cough responses to capsaicin were measured, and gastro-oesophageal reflux assessed by 24-h pH/impedance at screening. Results 22 patients were randomised to receive lesogaberan/placebo or placebo/lesogaberan (female (73%); mean±SD age 63.7±7.2 years; median (interquartile range) cough duration 10.5 (5.8–17.0) years; mean (95% CI) 45 (29–67) reflux events in 24 h; two patients had abnormal oesophageal acid exposure times). Although lesogaberan reduced cough counts by 26% over placebo, this did not reach statistical significance (p=0.12). However, lesogaberan did significantly improve cough responses to capsaicin (p=0.04) and the number of cough bouts (p=0.04) compared with placebo. Lesogaberan was well tolerated in this study. Conclusions Lesogaberan improved cough hypersensitivity and the number of bouts of coughing, but not coughs per hour. This implies a possible role for peripheral GABA
B receptors in refractory chronic cough.
AB - Objective Baclofen is a centrally acting γ-aminobutyric acid type B (GABA
B) receptor agonist which reduces gastro-oesophageal reflux and suppresses the cough reflex; however, central nervous system side-effects limit its use. Lesogaberan is a novel peripherally acting GABA
B agonist, but its effects on refractory chronic cough are unknown. Design We performed a single-centre, placebo-controlled, double-blind randomised crossover study in patients with chronic cough, refractory to the treatment of underlying conditions. Patients were randomised to treatment with lesogaberan 120 mg modified release twice daily or matched placebo for 2 weeks and then crossed over to the alternative therapy after a 2-week washout. The primary end-point was 24-h cough frequency measured with an acoustic monitoring system. In addition, cough responses to capsaicin were measured, and gastro-oesophageal reflux assessed by 24-h pH/impedance at screening. Results 22 patients were randomised to receive lesogaberan/placebo or placebo/lesogaberan (female (73%); mean±SD age 63.7±7.2 years; median (interquartile range) cough duration 10.5 (5.8–17.0) years; mean (95% CI) 45 (29–67) reflux events in 24 h; two patients had abnormal oesophageal acid exposure times). Although lesogaberan reduced cough counts by 26% over placebo, this did not reach statistical significance (p=0.12). However, lesogaberan did significantly improve cough responses to capsaicin (p=0.04) and the number of cough bouts (p=0.04) compared with placebo. Lesogaberan was well tolerated in this study. Conclusions Lesogaberan improved cough hypersensitivity and the number of bouts of coughing, but not coughs per hour. This implies a possible role for peripheral GABA
B receptors in refractory chronic cough.
UR - https://doi.org/10.1183/23120541.00546-2021
U2 - 10.1183/23120541.00546-2021
DO - 10.1183/23120541.00546-2021
M3 - Article
C2 - 35295236
VL - 8
SP - 546
EP - 2021
JO - European Respiratory Journal Open Research
JF - European Respiratory Journal Open Research
SN - 2312-0541
IS - 1
M1 - 00546-2021
ER -