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Hepatobiliary phenotypes of adults with alpha-1 antitrypsin deficiency
- 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.
- Subjects :
- Adult
Liver Cirrhosis
Male
medicine.medical_specialty
Cirrhosis
liver cirrhosis
liver
Gastroenterology
Cohort Studies
03 medical and health sciences
Liver disease
0302 clinical medicine
Cholelithiasis
Fibrosis
alpha 1-Antitrypsin Deficiency
Internal medicine
Diabetes mellitus
Genotype
Prevalence
medicine
Humans
cancer
Aged
Alpha 1-antitrypsin deficiency
business.industry
Liver Neoplasms
fibrosis
Cancer
Gallstones
Middle Aged
medicine.disease
United Kingdom
Phenotype
030228 respiratory system
Case-Control Studies
Female
030211 gastroenterology & hepatology
business
Subjects
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
- Full Text :
- https://doi.org/10.1136/gutjnl-2020-323729