Back to Search Start Over

Hepatobiliary phenotypes of adults with alpha-1 antitrypsin deficiency

Authors :
Alice M Turner
David A. Lomas
Alexa Nuñez
Sabina Janciauskiene
William J.H. Griffiths
Christian Trautwein
Joan Genescà
Michael Trauner
John R. Hurst
Jef Verbeek
Matthias C. Reichert
Guilherme Macedo
Ravi Mahadeva
Mònica Pons
Aleksander Krag
Rui Gaspar
V Pereira
Heinz Zoller
Catarina Gomes
Mattias Mandorfer
Barbara Burbaum
Frank Lammert
V Woditsch
Paul Ellis
Aileen Marshall
Douglas Thorburn
Nadine T. Gaisa
Karim Hamesch
Joanna Chorostowska-Wynimko
Luís Jasmins
Malin Fromme
Rodrigo Liberal
Pavel Strnad
Frederik Nevens
Noel G. McElvaney
Marc Miravitlles
Virginia Clark
Bibek Gooptu
Benedikt Schaefer
Katrine Holtz Thorhauge
Carolin V. Schneider
Nelia Abreu
Kai Markus Schneider
Federica Benini
Fromme, Malin [0000-0003-0382-5705]
Hamesch, Karim [0000-0002-1702-2746]
Reichert, Matthias C [0000-0002-8192-0575]
Mandorfer, Mattias [0000-0003-2330-0017]
Gaspar, Rui [0000-0003-0332-3844]
Trauner, Michael [0000-0002-1275-6425]
Krag, Aleksander [0000-0002-9598-4932]
Gooptu, Bibek [0000-0002-5223-1121]
Hurst, John R [0000-0002-7246-6040]
Lomas, David A [0000-0003-2339-6979]
Strnad, Pavel [0000-0002-7122-6379]
Apollo - University of Cambridge Repository
Source :
Fromme, M, Schneider, C V, Pereira, V, Hamesch, K, Pons, M, Reichert, M C, Benini, F, Ellis, P, H Thorhauge, K, Mandorfer, M, Burbaum, B, Woditsch, V, Chorostowska-Wynimko, J, Verbeek, J, Nevens, F, Genesca, J, Miravitlles, M, Nuñez, A, Schaefer, B, Zoller, H, Janciauskiene, S, Abreu, N, Jasmins, L, Gaspar, R, Gomes, C, Schneider, K M, Trauner, M, Krag, A, Gooptu, B, Thorburn, D, Marshall, A, Hurst, J R, Lomas, D A, Lammert, F, Gaisa, N T, Clark, V, Griffiths, W, Trautwein, C, Turner, A M, McElvaney, N G & Strnad, P 2022, ' Hepatobiliary phenotypes of adults with alpha-1 antitrypsin deficiency ', GUT, vol. 71, no. 2, pp. 415-423 . https://doi.org/10.1136/gutjnl-2020-323729
Publication Year :
2022

Abstract

ObjectiveAlpha-1 antitrypsin deficiency (AATD) is a common, potentially lethal inborn disorder caused by mutations in alpha-1 antitrypsin (AAT). Homozygosity for the ‘Pi*Z’ variant of AAT (Pi*ZZ genotype) causes lung and liver disease, whereas heterozygous ‘Pi*Z’ carriage (Pi*MZ genotype) predisposes to gallstones and liver fibrosis. The clinical significance of the more common ‘Pi*S’ variant remains largely undefined and no robust data exist on the prevalence of liver tumours in AATD.DesignBaseline phenotypes of AATD individuals and non-carriers were analysed in 482 380 participants in the UK Biobank. 1104 participants of a multinational cohort (586 Pi*ZZ, 239 Pi*SZ, 279 non-carriers) underwent a comprehensive clinical assessment. Associations were adjusted for age, sex, body mass index, diabetes and alcohol consumption.ResultsAmong UK Biobank participants, Pi*ZZ individuals displayed the highest liver enzyme values, the highest occurrence of liver fibrosis/cirrhosis (adjusted OR (aOR)=21.7 (8.8–53.7)) and primary liver cancer (aOR=44.5 (10.8–183.6)). Subjects with Pi*MZ genotype had slightly elevated liver enzymes and moderately increased odds for liver fibrosis/cirrhosis (aOR=1.7 (1.2–2.2)) and cholelithiasis (aOR=1.3 (1.2–1.4)). Individuals with homozygous Pi*S mutation (Pi*SS genotype) harboured minimally elevated alanine aminotransferase values, but no other hepatobiliary abnormalities. Pi*SZ participants displayed higher liver enzymes, more frequent liver fibrosis/cirrhosis (aOR=3.1 (1.1–8.2)) and primary liver cancer (aOR=6.6 (1.6–26.9)). The higher fibrosis burden was confirmed in a multinational cohort. Male sex, age ≥50 years, obesity and the presence of diabetes were associated with significant liver fibrosis.ConclusionOur study defines the hepatobiliary phenotype of individuals with the most relevant AATD genotypes including their predisposition to liver tumours, thereby allowing evidence-based advice and individualised hepatological surveillance.

Details

Language :
English
Database :
OpenAIRE
Journal :
Fromme, M, Schneider, C V, Pereira, V, Hamesch, K, Pons, M, Reichert, M C, Benini, F, Ellis, P, H Thorhauge, K, Mandorfer, M, Burbaum, B, Woditsch, V, Chorostowska-Wynimko, J, Verbeek, J, Nevens, F, Genesca, J, Miravitlles, M, Nuñez, A, Schaefer, B, Zoller, H, Janciauskiene, S, Abreu, N, Jasmins, L, Gaspar, R, Gomes, C, Schneider, K M, Trauner, M, Krag, A, Gooptu, B, Thorburn, D, Marshall, A, Hurst, J R, Lomas, D A, Lammert, F, Gaisa, N T, Clark, V, Griffiths, W, Trautwein, C, Turner, A M, McElvaney, N G & Strnad, P 2022, ' Hepatobiliary phenotypes of adults with alpha-1 antitrypsin deficiency ', GUT, vol. 71, no. 2, pp. 415-423 . https://doi.org/10.1136/gutjnl-2020-323729
Accession number :
edsair.doi.dedup.....e0bb0b61df320d870e692517692e26a5