PAI‐1 gain‐of‐function genotype, factors increasing PAI‐1 levels, and airway obstruction: The GALA II Cohort
Summary Background PAI‐1 gain‐of‐function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma. Objective We sought to determine whether the association of a gain‐of‐function polymorphism in plasminogen activator inhibitor‐1 (PAI‐1) wit...
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| Published in | Clinical and experimental allergy Vol. 47; no. 9; pp. 1150 - 1158 |
|---|---|
| Main Authors | , , , , , , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
Wiley Subscription Services, Inc
01.09.2017
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0954-7894 1365-2222 1365-2222 |
| DOI | 10.1111/cea.12958 |
Cover
| Abstract | Summary
Background
PAI‐1 gain‐of‐function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma.
Objective
We sought to determine whether the association of a gain‐of‐function polymorphism in plasminogen activator inhibitor‐1 (PAI‐1) with airway obstruction is modified by asthma status, and whether any genotype effect persists after accounting for common exposures that increase PAI‐1 level.
Methods
We studied 2070 Latino children (8‐21y) with genotypic and pulmonary function data from the GALA II cohort. We estimated the relationship of the PAI‐1 risk allele with FEV1/FVC by multivariate linear regression, stratified by asthma status. We examined the association of the polymorphism with asthma and airway obstruction within asthmatics via multivariate logistic regression. We replicated associations in the SAPPHIRE cohort of African Americans (n=1056). Secondary analysis included the effect of the at‐risk polymorphism on postbronchodilator lung function.
Results
There was an interaction between asthma status and the PAI‐1 polymorphism on FEV1/FVC (P=.03). The gain‐of‐function variants, genotypes (AA/AG), were associated with lower FEV1/FVC in subjects with asthma (β=−1.25, CI: −2.14,−0.35, P=.006), but not in controls. Subjects with asthma and the AA/AG genotypes had a 5% decrease in FEV1/FVC (P<.001). In asthmatics, the risk genotype (AA/AG) was associated with a 39% increase in risk of clinically relevant airway obstruction (OR=1.39, CI: 1.01, 1.92, P=.04). These associations persisted after exclusion of factors that increase PAI‐1 including tobacco exposure and obesity.
Conclusions and Clinical Relevance
The decrease in the FEV1/FVC ratio associated with the risk genotype was modified by asthma status. The genotype increased the odds of airway obstruction by 75% within asthmatics only. As exposures known to increase PAI‐1 levels did not mitigate this association, PAI‐1 may contribute to airway obstruction in the context of chronic asthmatic airway inflammation. |
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| AbstractList | PAI-1 gain-of-function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma.
We sought to determine whether the association of a gain-of-function polymorphism in plasminogen activator inhibitor-1 (PAI-1) with airway obstruction is modified by asthma status, and whether any genotype effect persists after accounting for common exposures that increase PAI-1 level.
We studied 2070 Latino children (8-21y) with genotypic and pulmonary function data from the GALA II cohort. We estimated the relationship of the PAI-1 risk allele with FEV1/FVC by multivariate linear regression, stratified by asthma status. We examined the association of the polymorphism with asthma and airway obstruction within asthmatics via multivariate logistic regression. We replicated associations in the SAPPHIRE cohort of African Americans (n=1056). Secondary analysis included the effect of the at-risk polymorphism on postbronchodilator lung function.
There was an interaction between asthma status and the PAI-1 polymorphism on FEV
/FVC (P=.03). The gain-of-function variants, genotypes (AA/AG), were associated with lower FEV
/FVC in subjects with asthma (β=-1.25, CI: -2.14,-0.35, P=.006), but not in controls. Subjects with asthma and the AA/AG genotypes had a 5% decrease in FEV
/FVC (P<.001). In asthmatics, the risk genotype (AA/AG) was associated with a 39% increase in risk of clinically relevant airway obstruction (OR=1.39, CI: 1.01, 1.92, P=.04). These associations persisted after exclusion of factors that increase PAI-1 including tobacco exposure and obesity.
The decrease in the FEV
/FVC ratio associated with the risk genotype was modified by asthma status. The genotype increased the odds of airway obstruction by 75% within asthmatics only. As exposures known to increase PAI-1 levels did not mitigate this association, PAI-1 may contribute to airway obstruction in the context of chronic asthmatic airway inflammation. Summary Background PAI-1 gain-of-function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma. Objective We sought to determine whether the association of a gain-of-function polymorphism in plasminogen activator inhibitor-1 (PAI-1) with airway obstruction is modified by asthma status, and whether any genotype effect persists after accounting for common exposures that increase PAI-1 level. Methods We studied 2070 Latino children (8-21y) with genotypic and pulmonary function data from the GALA II cohort. We estimated the relationship of the PAI-1 risk allele with FEV1/FVC by multivariate linear regression, stratified by asthma status. We examined the association of the polymorphism with asthma and airway obstruction within asthmatics via multivariate logistic regression. We replicated associations in the SAPPHIRE cohort of African Americans (n=1056). Secondary analysis included the effect of the at-risk polymorphism on postbronchodilator lung function. Results There was an interaction between asthma status and the PAI-1 polymorphism on FEV1/FVC (P=.03). The gain-of-function variants, genotypes (AA/AG), were associated with lower FEV1/FVC in subjects with asthma ([beta]=-1.25, CI: -2.14,-0.35, P=.006), but not in controls. Subjects with asthma and the AA/AG genotypes had a 5% decrease in FEV1/FVC (P<.001). In asthmatics, the risk genotype (AA/AG) was associated with a 39% increase in risk of clinically relevant airway obstruction (OR=1.39, CI: 1.01, 1.92, P=.04). These associations persisted after exclusion of factors that increase PAI-1 including tobacco exposure and obesity. Conclusions and Clinical Relevance The decrease in the FEV1/FVC ratio associated with the risk genotype was modified by asthma status. The genotype increased the odds of airway obstruction by 75% within asthmatics only. As exposures known to increase PAI-1 levels did not mitigate this association, PAI-1 may contribute to airway obstruction in the context of chronic asthmatic airway inflammation. Summary Background PAI‐1 gain‐of‐function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma. Objective We sought to determine whether the association of a gain‐of‐function polymorphism in plasminogen activator inhibitor‐1 (PAI‐1) with airway obstruction is modified by asthma status, and whether any genotype effect persists after accounting for common exposures that increase PAI‐1 level. Methods We studied 2070 Latino children (8‐21y) with genotypic and pulmonary function data from the GALA II cohort. We estimated the relationship of the PAI‐1 risk allele with FEV1/FVC by multivariate linear regression, stratified by asthma status. We examined the association of the polymorphism with asthma and airway obstruction within asthmatics via multivariate logistic regression. We replicated associations in the SAPPHIRE cohort of African Americans (n=1056). Secondary analysis included the effect of the at‐risk polymorphism on postbronchodilator lung function. Results There was an interaction between asthma status and the PAI‐1 polymorphism on FEV1/FVC (P=.03). The gain‐of‐function variants, genotypes (AA/AG), were associated with lower FEV1/FVC in subjects with asthma (β=−1.25, CI: −2.14,−0.35, P=.006), but not in controls. Subjects with asthma and the AA/AG genotypes had a 5% decrease in FEV1/FVC (P<.001). In asthmatics, the risk genotype (AA/AG) was associated with a 39% increase in risk of clinically relevant airway obstruction (OR=1.39, CI: 1.01, 1.92, P=.04). These associations persisted after exclusion of factors that increase PAI‐1 including tobacco exposure and obesity. Conclusions and Clinical Relevance The decrease in the FEV1/FVC ratio associated with the risk genotype was modified by asthma status. The genotype increased the odds of airway obstruction by 75% within asthmatics only. As exposures known to increase PAI‐1 levels did not mitigate this association, PAI‐1 may contribute to airway obstruction in the context of chronic asthmatic airway inflammation. PAI-1 gain-of-function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma.BACKGROUNDPAI-1 gain-of-function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma.We sought to determine whether the association of a gain-of-function polymorphism in plasminogen activator inhibitor-1 (PAI-1) with airway obstruction is modified by asthma status, and whether any genotype effect persists after accounting for common exposures that increase PAI-1 level.OBJECTIVEWe sought to determine whether the association of a gain-of-function polymorphism in plasminogen activator inhibitor-1 (PAI-1) with airway obstruction is modified by asthma status, and whether any genotype effect persists after accounting for common exposures that increase PAI-1 level.We studied 2070 Latino children (8-21y) with genotypic and pulmonary function data from the GALA II cohort. We estimated the relationship of the PAI-1 risk allele with FEV1/FVC by multivariate linear regression, stratified by asthma status. We examined the association of the polymorphism with asthma and airway obstruction within asthmatics via multivariate logistic regression. We replicated associations in the SAPPHIRE cohort of African Americans (n=1056). Secondary analysis included the effect of the at-risk polymorphism on postbronchodilator lung function.METHODSWe studied 2070 Latino children (8-21y) with genotypic and pulmonary function data from the GALA II cohort. We estimated the relationship of the PAI-1 risk allele with FEV1/FVC by multivariate linear regression, stratified by asthma status. We examined the association of the polymorphism with asthma and airway obstruction within asthmatics via multivariate logistic regression. We replicated associations in the SAPPHIRE cohort of African Americans (n=1056). Secondary analysis included the effect of the at-risk polymorphism on postbronchodilator lung function.There was an interaction between asthma status and the PAI-1 polymorphism on FEV1 /FVC (P=.03). The gain-of-function variants, genotypes (AA/AG), were associated with lower FEV1 /FVC in subjects with asthma (β=-1.25, CI: -2.14,-0.35, P=.006), but not in controls. Subjects with asthma and the AA/AG genotypes had a 5% decrease in FEV1 /FVC (P<.001). In asthmatics, the risk genotype (AA/AG) was associated with a 39% increase in risk of clinically relevant airway obstruction (OR=1.39, CI: 1.01, 1.92, P=.04). These associations persisted after exclusion of factors that increase PAI-1 including tobacco exposure and obesity.RESULTSThere was an interaction between asthma status and the PAI-1 polymorphism on FEV1 /FVC (P=.03). The gain-of-function variants, genotypes (AA/AG), were associated with lower FEV1 /FVC in subjects with asthma (β=-1.25, CI: -2.14,-0.35, P=.006), but not in controls. Subjects with asthma and the AA/AG genotypes had a 5% decrease in FEV1 /FVC (P<.001). In asthmatics, the risk genotype (AA/AG) was associated with a 39% increase in risk of clinically relevant airway obstruction (OR=1.39, CI: 1.01, 1.92, P=.04). These associations persisted after exclusion of factors that increase PAI-1 including tobacco exposure and obesity.The decrease in the FEV1 /FVC ratio associated with the risk genotype was modified by asthma status. The genotype increased the odds of airway obstruction by 75% within asthmatics only. As exposures known to increase PAI-1 levels did not mitigate this association, PAI-1 may contribute to airway obstruction in the context of chronic asthmatic airway inflammation.CONCLUSIONS AND CLINICAL RELEVANCEThe decrease in the FEV1 /FVC ratio associated with the risk genotype was modified by asthma status. The genotype increased the odds of airway obstruction by 75% within asthmatics only. As exposures known to increase PAI-1 levels did not mitigate this association, PAI-1 may contribute to airway obstruction in the context of chronic asthmatic airway inflammation. |
| Author | Galanter, J. Keoki Williams, L. Serebrisky, D. Borrell, L. N. Hu, D. Sen, S. Huntsman, S. Smith, L. J. Kalhan, R. Avila, P. C. Burchard, E. G. Cho, S. H. Min, J‐Y. Seibold, M. A. Levin, A. Sherenian, M. G. Rodriguez‐Santana, J. R. Kumar, R. Eng, C. Oh, S. S. |
| AuthorAffiliation | 7 Department of Medicine, University of California, San Francisco, CA, USA 1 Division of Allergy-Immunology, Department of Pediatrics, Northwestern University, Chicago, Illinois, USA 9 Centro de Neumologia Pediatrica, CSP, San Juan, PR, USA 12 Department of Health Sciences, Lehman College, CUNY, New York, NY, USA 5 Department of Public Health Science, Henry Ford Health System, Detroit, MI, USA 3 Division of Allergy-Immunology, Department of Medicine, Northwestern University, Chicago, Illinois; USA 13 Center for Genes, Environment and Health, National Jewish Health, Denver CO, USA 14 Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, USA 8 Division of Biostatistics, Department of Preventive Medicine, UTHSC, Memphis, TN, USA 15 Center for Health Policy and Health Services Research, Henry Ford Health System, Detroit, Michigan, USA 11 Division of Pulmonary Medicine, Department of Medicine, Northwestern University, Chicago, Illinois, USA 6 Department of Otolaryngology, North |
| AuthorAffiliation_xml | – name: 15 Center for Health Policy and Health Services Research, Henry Ford Health System, Detroit, Michigan, USA – name: 7 Department of Medicine, University of California, San Francisco, CA, USA – name: 6 Department of Otolaryngology, Northwestern University; Chicago, IL, USA – name: 2 The Ann and Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL, USA – name: 5 Department of Public Health Science, Henry Ford Health System, Detroit, MI, USA – name: 14 Department of Internal Medicine, Henry Ford Health System, Detroit, Michigan, USA – name: 10 Pediatric Pulmonary Division, Jacobi Medical Center, Bronx, NY, USA – name: 8 Division of Biostatistics, Department of Preventive Medicine, UTHSC, Memphis, TN, USA – name: 3 Division of Allergy-Immunology, Department of Medicine, Northwestern University, Chicago, Illinois; USA – name: 9 Centro de Neumologia Pediatrica, CSP, San Juan, PR, USA – name: 4 Division of Allergy-Immunology, Department of Internal Medicine, University of South Florida, Tampa, FL; USA – name: 1 Division of Allergy-Immunology, Department of Pediatrics, Northwestern University, Chicago, Illinois, USA – name: 12 Department of Health Sciences, Lehman College, CUNY, New York, NY, USA – name: 11 Division of Pulmonary Medicine, Department of Medicine, Northwestern University, Chicago, Illinois, USA – name: 13 Center for Genes, Environment and Health, National Jewish Health, Denver CO, USA |
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| Copyright | 2017 John Wiley & Sons Ltd 2017 John Wiley & Sons Ltd. Copyright © 2017 John Wiley & Sons Ltd |
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| Notes | Funding information Supported in part by the American Heart Association National Scientist Development Award and by the National Institutes of Health (K23 AI110731‐01 to SHC; R01‐ES015794, R01‐HL088133, R01‐HL078885, and R01‐HL104608, R01‐HL118267, R01‐AI077439, R01‐CA113710, R01‐AI079139); National Institute On Minority Health And Health Disparities of the National Institutes of Health under Award Number P60‐MD006902; the Flight Attendant Medical Research Institute (FAMRI), the Sandler Foundation (to E.G.B. and L.K.W.), the RWJF Amos Medical Faculty Development Award (to E.G.B.), and the American Asthma Foundation (to E.G.B. and L.K.W.). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These authors contributed equally to the manuscript. |
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Background
PAI‐1 gain‐of‐function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma.... PAI-1 gain-of-function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma. We sought to... Summary Background PAI-1 gain-of-function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma.... PAI-1 gain-of-function variants promote airway fibrosis and are associated with asthma and with worse lung function in subjects with asthma.BACKGROUNDPAI-1... |
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| SubjectTerms | Adolescent Adult Airway management Airway Obstruction - epidemiology Airway Obstruction - genetics Airway Obstruction - metabolism Airway Obstruction - physiopathology Alleles Asthma Asthma, Occupational - epidemiology Asthma, Occupational - genetics Asthma, Occupational - metabolism Asthma, Occupational - physiopathology Child Children Cohort Studies epidemiology Ethnicity Female Fibrosis Gain of Function Mutation Gene polymorphism Genetic Association Studies Genetic Predisposition to Disease Genotype Genotype & phenotype Humans Male Odds Ratio PAI‐1 pediatrics Plasminogen Activator Inhibitor 1 - genetics Plasminogen Activator Inhibitor 1 - metabolism Plasminogen activator inhibitors Polymorphism, Single Nucleotide Respiratory function Respiratory Function Tests Respiratory tract Respiratory tract diseases Tobacco Young Adult |
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| Title | PAI‐1 gain‐of‐function genotype, factors increasing PAI‐1 levels, and airway obstruction: The GALA II Cohort |
| URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcea.12958 https://www.ncbi.nlm.nih.gov/pubmed/28543872 https://www.proquest.com/docview/1933860563 https://www.proquest.com/docview/1903166062 https://pubmed.ncbi.nlm.nih.gov/PMC5764093 https://www.ncbi.nlm.nih.gov/pmc/articles/5764093 |
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