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The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypes.
- Source :
-
The European respiratory journal [Eur Respir J] 2020 Dec 10; Vol. 56 (6). Date of Electronic Publication: 2020 Dec 10 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Alpha-1 antitrypsin deficiency (AATD), mainly due to the PI*ZZ genotype in SERPINA1 , is one of the most common inherited diseases. Since it is associated with a high disease burden and partially prevented by smoking cessation, identification of PI*ZZ individuals through genotyping could improve health outcomes.We examined the frequency of the PI*ZZ genotype in individuals with and without diagnosed AATD from UK Biobank, and assessed the associations of the genotypes with clinical outcomes and mortality. A phenome-wide association study (PheWAS) was conducted to reveal disease associations with genotypes. A polygenic risk score (PRS) for forced expiratory volume in 1 s (FEV <subscript>1</subscript> )/forced vital capacity (FVC) ratio was used to evaluate variable penetrance of PI*ZZ.Among 458 164 European-ancestry participants in UK Biobank, 140 had the PI*ZZ genotype and only nine (6.4%, 95% CI 3.4-11.7%) of them were diagnosed with AATD. Those with PI*ZZ had a substantially higher odds of COPD (OR 8.8, 95% CI 5.8-13.3), asthma (OR 2.0, 95% CI 1.4-3.0), bronchiectasis (OR 7.3, 95%CI 3.2-16.8), pneumonia (OR 2.7, 95% CI 1.5-4.9) and cirrhosis (OR 7.8, 95% CI 2.5-24.6) diagnoses and a higher hazard of mortality (2.4, 95% CI 1.2-4.6), compared to PI*MM (wildtype) (n=398 424). These associations were stronger among smokers. PheWAS demonstrated associations with increased odds of empyema, pneumothorax, cachexia, polycythaemia, aneurysm and pancreatitis. Polygenic risk score and PI*ZZ were independently associated with FEV <subscript>1</subscript> /FVC <0.7 (OR 1.4 per 1-sd change, 95% CI 1.4-1.5 and OR 4.5, 95% CI 3.0-6.9, respectively).The important underdiagnosis of AATD, whose outcomes are partially preventable through smoking cession, could be improved through genotype-guided diagnosis.<br />Competing Interests: Conflict of interest: T. Nakanishi has nothing to disclose. Conflict of interest: V. Forgetta has nothing to disclose. Conflict of interest: T. Handa is in the employ of the Collaborative Research Laboratory funded by Teijin Pharma Co., Ltd. Conflict of interest: T. Hirai reports grants from The Intractable Respiratory Diseases and Pulmonary Hypertension Research Group, the Ministry of Health, Labor and Welfare, Japan, outside the submitted work. Conflict of interest: V. Mooser has nothing to disclose. Conflict of interest: G.M. Lathrop has nothing to disclose. Conflict of interest: W.O.C.M. Cookson has nothing to disclose. Conflict of interest: J.B. Richards has nothing to disclose.<br /> (Copyright ©ERS 2020.)
- Subjects :
- Cost of Illness
Genotype
Humans
alpha 1-Antitrypsin genetics
Pulmonary Disease, Chronic Obstructive diagnosis
Pulmonary Disease, Chronic Obstructive epidemiology
Pulmonary Disease, Chronic Obstructive genetics
Undiagnosed Diseases
alpha 1-Antitrypsin Deficiency complications
alpha 1-Antitrypsin Deficiency diagnosis
alpha 1-Antitrypsin Deficiency epidemiology
Subjects
Details
- Language :
- English
- ISSN :
- 1399-3003
- Volume :
- 56
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- The European respiratory journal
- Publication Type :
- Academic Journal
- Accession number :
- 32675199
- Full Text :
- https://doi.org/10.1183/13993003.01441-2020