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 inClinical and experimental allergy Vol. 47; no. 9; pp. 1150 - 1158
Main Authors Sherenian, M. G., Cho, S. H., Levin, A., Min, J‐Y., Oh, S. S., Hu, D., Galanter, J., Sen, S., Huntsman, S., Eng, C., Rodriguez‐Santana, J. R., Serebrisky, D., Avila, P. C., Kalhan, R., Smith, L. J., Borrell, L. N., Seibold, M. A., Keoki Williams, L., Burchard, E. G., Kumar, R.
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.09.2017
Subjects
Online AccessGet full text
ISSN0954-7894
1365-2222
1365-2222
DOI10.1111/cea.12958

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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.
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
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– name: 2 The Ann and Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL, USA
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CitedBy_id crossref_primary_10_1080_02770903_2022_2077218
crossref_primary_10_1021_acs_jpcb_9b06719
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2017 John Wiley & Sons Ltd.
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IsDoiOpenAccess true
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Issue 9
Keywords epidemiology
PAI-1
asthma
pediatrics
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
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.).
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These authors contributed equally to the manuscript.
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Snippet 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. 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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SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1150
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
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https://www.proquest.com/docview/1903166062
https://pubmed.ncbi.nlm.nih.gov/PMC5764093
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