Impact of Bronchiectasis on COPD Severity and Alpha-1 Antitrypsin Deficiency as a Risk Factor in Individuals with a Heavy Smoking History.

Rationale: Bronchiectasis is common among those with heavy smoking histories, but risk factors for bronchiectasis, including alpha-1 antitrypsin deficiency, and its implications for COPD severity are uncharacterized in such individuals. Objectives: To characterize the impact of bronchiectasis on COPD and explore alpha-1antitrypsin as a risk factor for bronchiectasis. Methods: SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS) participants (N=914; ages 40-80 years; &ge;20-pack-year smoking) had high-resolution computed tomography (CT) scans interpreted visually for bronchiectasis, based on airway dilation without fibrosis or cicatrization. We performed regression-based models of bronchiectasis with clinical outcomes and quantitative CT measures. We deeply sequenced the gene encoding -alpha-1 antitrypsin, <em>SERPINA1</em>, in 835 participants to test for rare variants, focusing on the PiZ genotype (Glu<sup>366</sup>Lys, rs28929474). Measurements and Main Results: We identified bronchiectasis in 365 (40%) participants, more frequently in women (45% versus 36%, <em>p</em>=0.0045), older participants (mean age=66[standard deviation (SD)=8.3] versus 64[SD=9.1] years, <em>p</em>=0.0083), and those with lower lung function (forced expiratory volume in 1 second [FEV<sub>1</sub> ] percentage predicted=66%[SD=27] versus 77%[SD=25], <em>p</em>&lt;0.0001; FEV<sub>1</sub> to forced vital capacity [FVC] ratio=0.54[0.17] versus 0.63[SD=0.16], <em>p</em>&lt;0.0001). Participants with bronchiectasis had greater emphysema (%voxels &le;-950 Hounsfield units, 11%[SD=12] versus 6.3%[SD=9], <em>p</em>&lt;0.0001) and parametric response mapping functional small airways disease (26[SD=15] versus 19[SD=15], <em>p</em>&lt;0.0001). Bronchiectasis was more frequent in the combined PiZZ and PiMZ genotype groups compared to those without PiZ, PiS, or other rare pathogenic variants (N=21 of 40 [52%] versus N=283 of 707[40%], odds ratio [OR]=1.97; 95% confidence interval [CI]=1.002, 3.90, <em>p</em>=0.049), an association attributed to White individuals (OR=1.98; 95%CI = 0.9956, 3.9; <em>p</em>=0.051). Conclusions: Bronchiectasis was common in those with heavy smoking histories and was associated with detrimental clinical and radiographic outcomes. Our findings support alpha-1antitrypsin guideline recommendations to screen for alpha-1 antitrypsin deficiency in an appropriate bronchiectasis subgroup with a significant smoking history.

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UNC Libraries
Published
2025-07-30
DOI
https://doi.org/10.17615/s8rm-zs56
Primary Topic
Chronic Obstructive Pulmonary Disease (COPD) Research
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article
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article

Impact of Bronchiectasis on COPD Severity and Alpha-1 Antitrypsin Deficiency as a Risk Factor in Individuals with a Heavy Smoking History.

Stephanie A. Christenson, Frank Genese, Manuel Izquierdo, Eric A. Hoffman et al.
UNC Libraries
Chronic Obstructive Pulmonary Disease (COPD) Research
article

Impact of Bronchiectasis on COPD Severity and Alpha-1 Antitrypsin Deficiency as a Risk Factor in Individuals with a Heavy Smoking History.

Stephanie A. Christenson, Frank Genese, Manuel Izquierdo, Eric A. Hoffman, John D. Newell, Igor Barjaktarević, MeiLan K. Han, Richard E. Kanner, R Graham Barr, Victor E. Ortega, Stephen P. Peters, Emily S. Wan, Jeffrey L. Curtis, Joe Zein, Wanda K. O’Neal, Xingnan Li, Prescott G. Woodruff, Nadia N. Hansel, Chad R. Marion, Robert Paine, David Couper, Fernando J. Martínez, Gregory A. Hawkins, Christopher B. Cooper, Eugene R Bleecker, Deborah A. Meyers
article en

Abstract

Rationale: Bronchiectasis is common among those with heavy smoking histories, but risk factors for bronchiectasis, including alpha-1 antitrypsin deficiency, and its implications for COPD severity are uncharacterized in such individuals. Objectives: To characterize the impact of bronchiectasis on COPD and explore alpha-1antitrypsin as a risk factor for bronchiectasis. Methods: SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS) participants (N=914; ages 40-80 years; &ge;20-pack-year smoking) had high-resolution computed tomography (CT) scans interpreted visually for bronchiectasis, based on airway dilation without fibrosis or cicatrization. We performed regression-based models of bronchiectasis with clinical outcomes and quantitative CT measures. We deeply sequenced the gene encoding -alpha-1 antitrypsin, <em>SERPINA1</em>, in 835 participants to test for rare variants, focusing on the PiZ genotype (Glu<sup>366</sup>Lys, rs28929474). Measurements and Main Results: We identified bronchiectasis in 365 (40%) participants, more frequently in women (45% versus 36%, <em>p</em>=0.0045), older participants (mean age=66[standard deviation (SD)=8.3] versus 64[SD=9.1] years, <em>p</em>=0.0083), and those with lower lung function (forced expiratory volume in 1 second [FEV<sub>1</sub> ] percentage predicted=66%[SD=27] versus 77%[SD=25], <em>p</em>&lt;0.0001; FEV<sub>1</sub> to forced vital capacity [FVC] ratio=0.54[0.17] versus 0.63[SD=0.16], <em>p</em>&lt;0.0001). Participants with bronchiectasis had greater emphysema (%voxels &le;-950 Hounsfield units, 11%[SD=12] versus 6.3%[SD=9], <em>p</em>&lt;0.0001) and parametric response mapping functional small airways disease (26[SD=15] versus 19[SD=15], <em>p</em>&lt;0.0001). Bronchiectasis was more frequent in the combined PiZZ and PiMZ genotype groups compared to those without PiZ, PiS, or other rare pathogenic variants (N=21 of 40 [52%] versus N=283 of 707[40%], odds ratio [OR]=1.97; 95% confidence interval [CI]=1.002, 3.90, <em>p</em>=0.049), an association attributed to White individuals (OR=1.98; 95%CI = 0.9956, 3.9; <em>p</em>=0.051). Conclusions: Bronchiectasis was common in those with heavy smoking histories and was associated with detrimental clinical and radiographic outcomes. Our findings support alpha-1antitrypsin guideline recommendations to screen for alpha-1 antitrypsin deficiency in an appropriate bronchiectasis subgroup with a significant smoking history.

UNC Libraries
University of North Carolina at Chapel Hill (US)
AstraZeneca, University of Washington, COPD Foundation, Australian Government, Mylan, National Institutes of Health, Gillings School of Public Health, University of North Carolina at Chapel Hill, National Heart, Lung, and Blood Institute
Openalex Percentile: Top 63%
Chronic Obstructive Pulmonary Disease (COPD) Research
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