Heterogeneous burden of lung disease in smokers with borderline airflow obstruction
Author
Pirozzi, Cheryl SGu, Tian
Quibrera, Pedro M
Carretta, Elizabeth E
Han, MeiLan K
Murray, Susan
Cooper, Christopher B
Tashkin, Donald P
Kleerup, Eric C
Barjaktarevic, Igor
Hoffman, Eric A
Martinez, Carlos H
Christenson, Stephanie A
Hansel, Nadia N
Graham Barr, R
Bleecker, Eugene R
Ortega, Victor E
Martinez, Fernando J
Kanner, Richard E
Paine, Robert
Affiliation
Univ Arizona, Dept MedIssue Date
2018-11-20Keywords
Airway obstructionChronic obstructive pulmonary disease
Emphysema
Forced expiratory volume
Maximal Midexpiratory flow rate
Pulmonary function tests
Spirometry
Metadata
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BMCCitation
Pirozzi, C. S., Gu, T., Quibrera, P. M., Carretta, E. E., Han, M. K., Murray, S., ... & Hoffman, E. A. (2018). Heterogeneous burden of lung disease in smokers with borderline airflow obstruction. Respiratory research, 19(1), 223.Journal
RESPIRATORY RESEARCHRights
© The Author(s). 2018. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
The identification of smoking-related lung disease in current and former smokers with normal FEV1 is complex, leading to debate regarding using a ratio of forced expiratory volume in 1 s to forced vital capacity (FEV1/FVC) of less than 0.70 versus the predicted lower limit of normal (LLN) for diagnosis of airflow obstruction. We hypothesized that the discordant group of ever-smokers with FEV1/FVC between the LLN and 0.70 is heterogeneous, and aimed to characterize the burden of smoking-related lung disease in this group.Note
Open Access Journal.ISSN
1465-993XPubMed ID
30454050Version
Final published versionSponsors
NIH/NHLBI [HHSN268200900013C, HHSN268200900014C, HHSN268200900015C, HHSN268200900016C, HHSN268200900017C, HHSN268200900018C, HHSN268200900019C, HHSN268200900020C]; AstraZeneca; Bellerophon Therapeutics; Boehringer-Ingelheim Pharmaceuticals, Inc.; Chiesi Farmaceutici SpA; Forest Research Institute, Inc.; GSK; Grifols Therapeutics, Inc.; Ikaria, Inc.; Nycomed GmbH; Takeda Pharmaceutical Company; Novartis Pharmaceuticals Corporation; Regeneron Pharmaceuticals, Inc.; Sanofi; [R01 HL122438]; [K24 HL138188]ae974a485f413a2113503eed53cd6c53
10.1186/s12931-018-0911-z
Scopus Count
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Except where otherwise noted, this item's license is described as © The Author(s). 2018. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).
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