TY - JOUR
T1 - Seven Pillars of Small Airways Disease in Asthma and COPD
T2 - Supporting Opportunities for Novel Therapies
AU - Usmani, Omar S.
AU - Han, Mei Lan K.
AU - Kaminsky, David A.
AU - Hogg, James
AU - Hjoberg, Josephine
AU - Patel, Naimish
AU - Hardin, Megan
AU - Keen, Christina
AU - Rennard, Stephen
AU - Blé, François Xavier
AU - Brown, Mary N.
N1 - Funding Information:
FUNDING/SUPPORT: This review was funded by AstraZeneca.Financial/nonfinancial disclosures: The authors have reported to CHEST the following: O. S. U. received grants from AstraZeneca, Boehringer Ingelheim, Chiesi, Edmond Pharma, and GlaxoSmithKline; and personal fees from Aerocrine, AstraZeneca, Boehringer Ingelheim, Chiesi, Cipla, Mundipharma, Napp, Novartis, Pearl Therapeutics, Sandoz, Takeda, and Zentiva outside the submitted work. M. K. H. received personal fees from AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, Merck, and Mylan; and research support from Novartis, Sunovion, and National Institutes of Health outside the submitted work. D. A. K. received personal fees from MGC Diagnostics Inc. outside the submitted work. Jo. H. was an employee of AstraZeneca from 2012 to 2017; and is a shareholder of AstraZeneca. N. P. is an employee of Sanofi Pharmaceuticals. M. H. is an employee of Sanofi Genzyme. C. K. F. -X. B. and M. N. B. are employees and shareholders of AstraZeneca. S. R. was an employee of AstraZeneca from 2015 to 2019 and has consulted with GSK, Verona, NovoVentures and Bergenbio. None declared (Ja. H.). Role of sponsors: The sponsor had no role in the design of the study, the collection and analysis of the data, or the preparation of the manuscript. Other contributions: Medical writing support, under the direction of the authors, was provided by Richard Knight, PhD, CMC Connect, McCann Health Medical Communications, and funded by AstraZeneca in accordance with Good Publication Practice (GPP3) guidelines (Ann Intern Med. 2015;163:461-464).
Funding Information:
Other contributions: Medical writing support, under the direction of the authors, was provided by Richard Knight, PhD, CMC Connect, McCann Health Medical Communications, and funded by AstraZeneca in accordance with Good Publication Practice (GPP3) guidelines (Ann Intern Med. 2015;163:461-464).
Publisher Copyright:
© 2021
PY - 2021/7
Y1 - 2021/7
N2 - Identification of pathologic changes in early and mild obstructive lung disease has shown the importance of the small airways and their contribution to symptoms. Indeed, significant small airways dysfunction has been found prior to any overt airway obstruction being detectable by conventional spirometry techniques. However, most therapies for the treatment of obstructive lung disease target the physiological changes and associated symptoms that result from chronic lung disease, rather than directly targeting the specific underlying causes of airflow disruption or the drivers of disease progression. In addition, although spirometry is the current standard for diagnosis and monitoring of response to therapy, the most widely used measure, FEV1, does not align with the pathologic changes in early or mild disease and may not align with symptoms or exacerbation frequency in the individual patient. Newer functional and imaging techniques allow more effective assessment of small airways dysfunction; however, significant gaps in our understanding remain. Improving our knowledge of the role of small airways dysfunction in early disease in the airways, along with the identification of novel end points to measure subclinical changes in this region (ie, those not captured as symptoms or identified through standard FEV1), may lead to the development of novel therapies that directly combat early airways disease processes with a view to slowing disease progression and reversing damage. This expert opinion paper discusses small airways disease in the context of asthma and COPD and highlights gaps in current knowledge that impede earlier identification of obstructive lung disease and the development and standardization of novel small airways-specific end points for use in clinical trials.
AB - Identification of pathologic changes in early and mild obstructive lung disease has shown the importance of the small airways and their contribution to symptoms. Indeed, significant small airways dysfunction has been found prior to any overt airway obstruction being detectable by conventional spirometry techniques. However, most therapies for the treatment of obstructive lung disease target the physiological changes and associated symptoms that result from chronic lung disease, rather than directly targeting the specific underlying causes of airflow disruption or the drivers of disease progression. In addition, although spirometry is the current standard for diagnosis and monitoring of response to therapy, the most widely used measure, FEV1, does not align with the pathologic changes in early or mild disease and may not align with symptoms or exacerbation frequency in the individual patient. Newer functional and imaging techniques allow more effective assessment of small airways dysfunction; however, significant gaps in our understanding remain. Improving our knowledge of the role of small airways dysfunction in early disease in the airways, along with the identification of novel end points to measure subclinical changes in this region (ie, those not captured as symptoms or identified through standard FEV1), may lead to the development of novel therapies that directly combat early airways disease processes with a view to slowing disease progression and reversing damage. This expert opinion paper discusses small airways disease in the context of asthma and COPD and highlights gaps in current knowledge that impede earlier identification of obstructive lung disease and the development and standardization of novel small airways-specific end points for use in clinical trials.
KW - COPD
KW - MRI
KW - asthma
KW - oscillometry
KW - respiratory function tests
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U2 - 10.1016/j.chest.2021.03.047
DO - 10.1016/j.chest.2021.03.047
M3 - Review article
C2 - 33819471
AN - SCOPUS:85109117439
SN - 0012-3692
VL - 160
SP - 114
EP - 134
JO - Diseases of the chest
JF - Diseases of the chest
IS - 1
ER -