TY - JOUR
T1 - Alpha-1 antitrypsin deficiency and Pi*S and Pi*Z SERPINA1 variants are associated with asthma exacerbations
AU - Martín-González, Elena
AU - Hernández-Pérez, José M
AU - Pérez, José A Pérez
AU - Pérez-García, Javier
AU - Herrera-Luis, Esther
AU - González-Pérez, Ruperto
AU - González-González, Orelvis
AU - Mederos-Luis, Elena
AU - Sánchez-Machín, Inmaculada
AU - Poza-Guedes, Paloma
AU - Sardón, Olaia
AU - Corcuera, Paula
AU - Cruz, María J
AU - González-Barcala, Francisco J
AU - Martínez-Rivera, Carlos
AU - Mullol, Joaquim
AU - Muñoz, Xavier
AU - Olaguibel, José M
AU - Plaza, Vicente
AU - Quirce, Santiago
AU - Valero, Antonio
AU - Sastre, Joaquín
AU - Korta-Murua, Javier
AU - Del Pozo, Victoria
AU - Lorenzo-Díaz, Fabián
AU - Villar, Jesús
AU - Pino-Yanes, María
AU - González-Carracedo, Mario A
N1 - Copyright © 2023 Sociedade Portuguesa de Pneumologia. Published by Elsevier España, S.L.U. All rights reserved.
Publisher Copyright:
© 2023 Sociedade Portuguesa de Pneumologia
PY - 2023/5/24
Y1 - 2023/5/24
N2 - Introduction and objectives: Asthma is a chronic inflammatory disease of the airways. Asthma patients may experience potentially life-threatening episodic flare-ups, known as exacerbations, which may significantly contribute to the asthma burden. The Pi*S and Pi*Z variants of the SERPINA1 gene, which usually involve alpha-1 antitrypsin (AAT) deficiency, had previously been associated with asthma. The link between AAT deficiency and asthma might be represented by the elastase/antielastase imbalance. However, their role in asthma exacerbations remains unknown. Our objective was to assess whether SERPINA1 genetic variants and reduced AAT protein levels are associated with asthma exacerbations. Materials and methods: In the discovery analysis, SERPINA1 Pi*S and Pi*Z variants and serum AAT levels were analyzed in 369 subjects from La Palma (Canary Islands, Spain). As replication, genomic data from two studies focused on 525 Spaniards and publicly available data from UK Biobank, FinnGen, and GWAS Catalog (Open Targets Genetics) were analyzed. The associations between SERPINA1 Pi*S and Pi*Z variants and AAT deficiency with asthma exacerbations were analyzed with logistic regression models, including age, sex, and genotype principal components as covariates. Results: In the discovery, a significant association with asthma exacerbations was found for both Pi*S (odds ratio [OR]=2.38, 95% confidence interval [CI]= 1.40–4.04, p-value=0.001) and Pi*Z (OR=3.49, 95%CI=1.55–7.85, p-value=0.003)Likewise, AAT deficiency was associated with a higher risk for asthma exacerbations (OR=5.18, 95%CI=1.58–16.92, p-value=0.007) as well as AAT protein levels (OR= 0.72, 95%CI=0.57–0.91, p-value=0.005). The Pi*Z association with exacerbations was replicated in samples from Spaniards with two generations of Canary Islander origin (OR=3.79, p-value=0.028), and a significant association with asthma hospitalizations was found in the Finnish population (OR=1.12, p-value=0.007). Conclusions: AAT deficiency could be a potential therapeutic target for asthma exacerbations in specific populations.
AB - Introduction and objectives: Asthma is a chronic inflammatory disease of the airways. Asthma patients may experience potentially life-threatening episodic flare-ups, known as exacerbations, which may significantly contribute to the asthma burden. The Pi*S and Pi*Z variants of the SERPINA1 gene, which usually involve alpha-1 antitrypsin (AAT) deficiency, had previously been associated with asthma. The link between AAT deficiency and asthma might be represented by the elastase/antielastase imbalance. However, their role in asthma exacerbations remains unknown. Our objective was to assess whether SERPINA1 genetic variants and reduced AAT protein levels are associated with asthma exacerbations. Materials and methods: In the discovery analysis, SERPINA1 Pi*S and Pi*Z variants and serum AAT levels were analyzed in 369 subjects from La Palma (Canary Islands, Spain). As replication, genomic data from two studies focused on 525 Spaniards and publicly available data from UK Biobank, FinnGen, and GWAS Catalog (Open Targets Genetics) were analyzed. The associations between SERPINA1 Pi*S and Pi*Z variants and AAT deficiency with asthma exacerbations were analyzed with logistic regression models, including age, sex, and genotype principal components as covariates. Results: In the discovery, a significant association with asthma exacerbations was found for both Pi*S (odds ratio [OR]=2.38, 95% confidence interval [CI]= 1.40–4.04, p-value=0.001) and Pi*Z (OR=3.49, 95%CI=1.55–7.85, p-value=0.003)Likewise, AAT deficiency was associated with a higher risk for asthma exacerbations (OR=5.18, 95%CI=1.58–16.92, p-value=0.007) as well as AAT protein levels (OR= 0.72, 95%CI=0.57–0.91, p-value=0.005). The Pi*Z association with exacerbations was replicated in samples from Spaniards with two generations of Canary Islander origin (OR=3.79, p-value=0.028), and a significant association with asthma hospitalizations was found in the Finnish population (OR=1.12, p-value=0.007). Conclusions: AAT deficiency could be a potential therapeutic target for asthma exacerbations in specific populations.
KW - Asthma
KW - Exacerbations
KW - SERPINA 1
KW - Alpha-1 antitrypsin
KW - Dediciency
KW - Alpha-1 antitrypsin deficiency
KW - SERPINA1
UR - http://www.scopus.com/inward/record.url?scp=85160244825&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/9e4d3b37-351a-36ea-8bf4-800c3061ede7/
U2 - 10.1016/j.pulmoe.2023.05.002
DO - 10.1016/j.pulmoe.2023.05.002
M3 - Article
C2 - 37236906
SN - 2531-0429
JO - Pulmonology
JF - Pulmonology
ER -