Clinical Phenotypes of Atopy and Asthma in COPD A Meta-analysis of SPIROMICS and COPDGene

被引:21
作者
Putcha, Nirupama [1 ]
Fawzy, Ashraf [1 ]
Matsui, Elizabeth C. [2 ,3 ]
Liu, Mark C. [1 ]
Bowler, Russ P. [4 ]
Woodruff, Prescott G. [5 ]
O'Neal, Wanda K. [6 ]
Comellas, Alejandro P. [7 ]
Han, MeiLan K. [8 ]
Dransfield, Mark T. [9 ,10 ]
Wells, J. Michael [9 ,10 ]
Lugogo, Njira [8 ]
Gao, Li [11 ]
Talbot, C. Conover [12 ]
Hoffman, Eric A. [7 ]
Cooper, Christopher B. [13 ]
Paulin, Laura M. [14 ]
Kanner, Richard E. [15 ]
Criner, Gerard [16 ]
Ortega, Victor E. [17 ]
Barr, R. Graham [18 ]
Krishnan, Jerry A. [19 ]
Martinez, Fernando J. [20 ]
Drummond, M. Bradley [21 ]
Wise, Robert A. [1 ]
Diette, Gregory B. [1 ]
Hersh, Craig P. [22 ]
Hansel, Nadia N. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Div Pulm & Crit Care Med, Baltimore, MD USA
[2] Univ Texas Austin, Dept Populat Hlth, Dell Med Sch, Austin, TX USA
[3] Univ Texas Austin, Dept Pediat, Dell Med Sch, Austin, TX USA
[4] Natl Jewish Hlth, Div Pulm Crit Care & Sleep Med, Denver, CO USA
[5] Univ Calif San Francisco, Div Pulm Crit Care & Sleep, San Francisco, CA 94143 USA
[6] Univ N Carolina, Marsico Lung Inst, Chapel Hill, NC 27515 USA
[7] Univ Iowa, Div Pulm Crit Care & Occupat Med, Iowa City, IA USA
[8] Univ Michigan, Sch Med, Div Pulm & Crit Care Med, Ann Arbor, MI USA
[9] Univ Alabama Birmingham, Lung Hlth Ctr, Birmingham, AL USA
[10] Birmingham VA Med Ctr, Birmingham, AL USA
[11] Johns Hopkins Univ, Div Allergy & Clin Immunol, Baltimore, MD USA
[12] Johns Hopkins Sch Med, Inst Basic Biomed Sci, Baltimore, MD USA
[13] Univ Calif Los Angeles, Div Pulm & Crit Care, Los Angeles, CA USA
[14] Dartmouth Hitchcock Med Ctr, Geisel Sch Med Dartmouth, Sect Pulm & Crit Care Med, Lebanon, NH 03766 USA
[15] Univ Utah, Sch Med, Div Pulm & Crit Care, Salt Lake City, UT USA
[16] Temple Univ, Dept Pulm, Philadelphia, PA USA
[17] Wake Forest Sch Med, Dept Internal Med, Winston Salem, NC 27101 USA
[18] Columbia Univ, Div Gen Internal Med, Med Ctr, New York, NY USA
[19] Univ Illinois, Div Pulm Crit Care Sleep & Allergy, Chicago, IL USA
[20] Univ N Carolina, Div Pulm & Crit Care Med, Chapel Hill, NC 27515 USA
[21] Univ N Carolina, Well Cornell Med, New York Presbyterian Hosp, Div Pulm Dis & Crit Care Med, Chapel Hill, NC 27515 USA
[22] Brigham & Womens Hosp, Channing Div Network Med, 75 Francis St, Boston, MA 02115 USA
关键词
asthma COPD overlap; atopy; COPD; INCREASED RISK; OVERLAP SYNDROME; EXACERBATIONS; FEATURES; DISEASE;
D O I
10.1016/j.chest.2020.04.069
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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.
引用
收藏
页码:2333 / 2345
页数:13
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