TY - JOUR
T1 - Clinical Phenotypes of Atopy and Asthma in COPD
T2 - A Meta-analysis of SPIROMICS and COPDGene
AU - Putcha, Nirupama
AU - Fawzy, Ashraf
AU - Matsui, Elizabeth C.
AU - Liu, Mark C.
AU - Bowler, Russ P.
AU - Woodruff, Prescott G.
AU - O'Neal, Wanda K.
AU - Comellas, Alejandro P.
AU - Han, Mei Lan K.
AU - Dransfield, Mark T.
AU - Wells, J. Michael
AU - Lugogo, Njira
AU - Gao, Li
AU - Talbot, C Conover
AU - Hoffman, Eric A.
AU - Cooper, Christopher B.
AU - Paulin, Laura
AU - Kanner, Richard E.
AU - Criner, Gerard
AU - Ortega, Victor E.
AU - Barr, R. Graham
AU - Krishnan, Jerry A.
AU - Martinez, Fernando J.
AU - Drummond, M. Bradley
AU - Wise, Robert A.
AU - Diette, Gregory B.
AU - Hersh, Craig P.
AU - Hansel, Nadia N.
N1 - Funding Information:
FUNDING/SUPPORT: N. P. is supported by K23HL123594. E. C. M. is supported by K24AI114769. C. P. H. is supported by R01HL130512, R01HL125583. SPIROMICS was supported by contracts from the NIH/NHLBI (HHSN268200900013C, HHSN268200900014C, HHSN268200900015C, HHSN268200900016C, HHSN268200900017C, HHSN268200900018C, HHSN268200900019C, HHSN268200900020C), and grants from the NIH/NHLBI (U01 HL137880 and U24 HL141762), supplemented by contributions made through the Foundation for the NIH and the COPD Foundation from AstraZeneca/MedImmune; Bayer; Bellerophon Therapeutics; BoehringerIngelheim Pharmaceuticals, Inc.; Chiesi Farmaceutici S.p.A.; Forest Research Institute, Inc.; GlaxoSmithKline; Grifols Therapeutics, Inc.; Ikaria, Inc.; Novartis Pharmaceuticals Corporation; Nycomed GmbH; ProterixBio; Regeneron Pharmaceuticals, Inc; Sanofi; Sunovion; Takeda Pharmaceutical Company; Theravance Biopharma; and Mylan. COPDGene is supported by NHLBI U01 HL089897 and U01 HL089856. The COPDGene study (NCT00608764) is also supported by the COPD Foundation through contributions made to an Industry Advisory Committee comprising AstraZeneca, Boehringer-Ingelheim, GlaxoSmithKline, Novartis, and Sunovion. N. N. H. is supported by P50MD010431 (PI NNH), R01ES022607 (PI NNH), EPA agreement number 83615001.
Funding Information:
Financial/nonfinancial disclosures: The authors have reported to CHEST the following: R. A. W. reports personal fees from GlaxoSmithKline, AstraZeneca, Boehringer Ingelheim, Novartis, Contrafect, Pulmonx, Spiration, Sunovion, Merck, Circassia, Verona, Mylan, Theravance, Propeller Health, and AbbVie outside the scope of the submitted work. M. K. H. reports consulting for BI, AZ, GSK, Merck, and Mylan; and research support from Novartis and Sunovion. C. P. H. reports grant support from Boehringer-Ingelheim and Novartis. J. A. K. reports research funding from NIH/NHLBI, PCORI, and ResMed/Inogen. A. P. C. reports paid consulting for VIDA. E. A. H. is a founder and shareholder of VIDA Diagnostics, a company commercializing lung image analysis software developed, in part, at the University of Iowa. M. T. D. reports grant funding from NIH/NHLBI. P. G. W. reports consulting income from GSK, Genentech, Theravance, Astra Zeneca, Glenmark, 23andme, Sanofi, Regeneron. C. B. C. reports personal fees from GlaxoSmithKline, PulmonX, Nuvaira and MGC Diagnostics. None declared (N. P., A. F., E. C. M., M. C. L., R. P. B., W. K. O., J. M. W., N. L., L. G., C. C. T., L. M. P., R. E. K., G. C., V. E. O., R. G. B., F. J. M., M. B. D., G. B. D., N. N. H.)
Publisher Copyright:
© 2020 American College of Chest Physicians
PY - 2020/12
Y1 - 2020/12
N2 - Background: Little is known about the concordance of atopy with asthma COPD overlap. Among individuals with COPD, a better understanding of the phenotypes characterized by asthma overlap and atopy is needed to better target therapies. Research Question: What is the overlap between atopy and asthma status among individuals with COPD, and how are categories defined by the presence of atopy and asthma status associated with clinical and radiologic phenotypes and outcomes in the Genetic Epidemiology of COPD Study (COPDGene) and Subpopulation and Intermediate Outcome Measures in COPD Study (SPIROMICS)? Study Design and Methods: Four hundred three individuals with COPD from SPIROMICS and 696 individuals from COPDGene with data about specific IgEs to 10 common allergens and mixes (simultaneous assessment of combination of allergens in similar category) were included. Comparison groups were defined by atopic and asthma status (neither, atopy alone, atopic asthma, nonatopic asthma, with atopy defined as any positive specific IgE (≥0.35 KU/L) to any of the 10 allergens or mixes and asthma defined as self-report of doctor-diagnosed current asthma). Multivariable regression analyses (linear, logistic, and zero inflated negative binomial where appropriate) adjusted for age, sex, race, lung function, smoking status, pack-years smoked, and use of inhaled corticosteroids were used to determine characteristics of groups and relationship with outcomes (exacerbations, clinical outcomes, CT metrics) separately in COPDGene and SPIROMICS, and then adjusted results were combined using meta-analysis. Results: The prevalence of atopy was 35% and 36% in COPD subjects from SPIROMICS and COPDGene, respectively, and less than 50% overlap was seen between atopic status with asthma in both cohorts. In meta-analysis, individuals with nonatopic asthma had the most impaired symptom scores (effect size for St. George's Respiratory Questionnaire total score, 4.2; 95% CI, 0.4-7.9; effect size for COPD Assessment Test score, 2.8; 95% CI, 0.089-5.4), highest risk for exacerbations (incidence rate ratio, 1.41; 95% CI, 1.05-1.88) compared with the group without atopy or asthma. Those with atopy and atopic asthma were not at increased risk for adverse outcomes. Interpretation: Asthma and atopy had incomplete overlap among former and current smokers with COPD in COPDGene and SPIROMICS. Nonatopic asthma was associated with adverse outcomes and exacerbation risk in COPD, whereas groups having atopy alone and atopic asthma had less risk.
AB - Background: Little is known about the concordance of atopy with asthma COPD overlap. Among individuals with COPD, a better understanding of the phenotypes characterized by asthma overlap and atopy is needed to better target therapies. Research Question: What is the overlap between atopy and asthma status among individuals with COPD, and how are categories defined by the presence of atopy and asthma status associated with clinical and radiologic phenotypes and outcomes in the Genetic Epidemiology of COPD Study (COPDGene) and Subpopulation and Intermediate Outcome Measures in COPD Study (SPIROMICS)? Study Design and Methods: Four hundred three individuals with COPD from SPIROMICS and 696 individuals from COPDGene with data about specific IgEs to 10 common allergens and mixes (simultaneous assessment of combination of allergens in similar category) were included. Comparison groups were defined by atopic and asthma status (neither, atopy alone, atopic asthma, nonatopic asthma, with atopy defined as any positive specific IgE (≥0.35 KU/L) to any of the 10 allergens or mixes and asthma defined as self-report of doctor-diagnosed current asthma). Multivariable regression analyses (linear, logistic, and zero inflated negative binomial where appropriate) adjusted for age, sex, race, lung function, smoking status, pack-years smoked, and use of inhaled corticosteroids were used to determine characteristics of groups and relationship with outcomes (exacerbations, clinical outcomes, CT metrics) separately in COPDGene and SPIROMICS, and then adjusted results were combined using meta-analysis. Results: The prevalence of atopy was 35% and 36% in COPD subjects from SPIROMICS and COPDGene, respectively, and less than 50% overlap was seen between atopic status with asthma in both cohorts. In meta-analysis, individuals with nonatopic asthma had the most impaired symptom scores (effect size for St. George's Respiratory Questionnaire total score, 4.2; 95% CI, 0.4-7.9; effect size for COPD Assessment Test score, 2.8; 95% CI, 0.089-5.4), highest risk for exacerbations (incidence rate ratio, 1.41; 95% CI, 1.05-1.88) compared with the group without atopy or asthma. Those with atopy and atopic asthma were not at increased risk for adverse outcomes. Interpretation: Asthma and atopy had incomplete overlap among former and current smokers with COPD in COPDGene and SPIROMICS. Nonatopic asthma was associated with adverse outcomes and exacerbation risk in COPD, whereas groups having atopy alone and atopic asthma had less risk.
KW - COPD
KW - asthma COPD overlap
KW - atopy
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U2 - 10.1016/j.chest.2020.04.069
DO - 10.1016/j.chest.2020.04.069
M3 - Article
C2 - 32450244
AN - SCOPUS:85096577699
SN - 0012-3692
VL - 158
SP - 2333
EP - 2345
JO - CHEST
JF - CHEST
IS - 6
ER -