Literature DB >> 24518491

Pi*Z heterozygous alpha-1 antitrypsin states accelerate parenchymal but not biliary cirrhosis.

Tessa M Cacciottolo1, William T H Gelson, Gerald Maguire, Susan E Davies, William J H Griffiths.   

Abstract

OBJECTIVE: The degree to which heterozygous forms of alpha-1 antitrypsin (A1AT), principally MZ, causes liver disease is uncertain. If heterozygosity is a relevant cofactor, over-representation in patients with end-stage liver disease would be predicted. We therefore assessed the prevalence and disease-related distribution of A1AT heterozygosity in the largest cohort to date for this purpose.
METHODS: We retrospectively analysed 1036 patients assessed for liver transplantation at our unit between 2003 and 2010. A1AT heterozygotes were identified on the basis of isoelectric focusing and/or histology, showing A1AT globule deposition consistent with an abnormal phenotype.
RESULTS: Z-allele frequency was the highest in patients with nonalcoholic steatohepatitis (NASH) cirrhosis (20.3%), followed by patients with 'other parenchymal' diseases (11.9%), alcohol-related liver disease (9.9%), autoimmune disease (8.6%), hepatitis C (6.1%), hepatitis B (3.0%) and biliary disease (1.9%). Compared with the heterozygote frequency in the general European population of 9.0%, the heterozygote frequency was significantly higher among patients with NASH cirrhosis (P≤0.0001) and lower in the biliary subgroup (P=0.004). The prevalence of MZ heterozygosity was significantly increased in cirrhosis because of both alcohol (9.9%) and NASH (17.3%) compared with the general European population (2.8%; P<0.0001).
CONCLUSION: Accumulation of misfolded A1AT aggregates appears to accelerate progression, in which the hepatocyte is the key injured cell. Heterozygous A1AT states worsen prognosis, particularly in NASH and alcohol-related cirrhosis, and should be identified at presentation. In cases in which genetic screening is not readily available, a low threshold for isoelectric focusing and routine specific histochemical staining of liver biopsy specimens are warranted to identify these patients.

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Year:  2014        PMID: 24518491     DOI: 10.1097/MEG.0000000000000061

Source DB:  PubMed          Journal:  Eur J Gastroenterol Hepatol        ISSN: 0954-691X            Impact factor:   2.566


  4 in total

1.  The Alpha-1 Antitrypsin Polymer Load Correlates With Hepatocyte Senescence, Fibrosis Stage and Liver-Related Mortality.

Authors:  Marianna Mela; Wendy Smeeton; Susan E Davies; Elena Miranda; Cinzia Scarpini; Nick Coleman; Graeme J M Alexander
Journal:  Chronic Obstr Pulm Dis       Date:  2020-07

2.  Heterozygosity for the alpha-1-antitrypsin Z allele in cirrhosis is associated with more advanced disease.

Authors:  Benedikt Schaefer; Mattias Mandorfer; André Viveiros; Armin Finkenstedt; Peter Ferenci; Stefan Schneeberger; Herbert Tilg; Heinz Zoller
Journal:  Liver Transpl       Date:  2018-05-14       Impact factor: 5.799

3.  Z-α1-antitrypsin polymers impose molecular filtration in the endoplasmic reticulum after undergoing phase transition to a solid state.

Authors:  Joseph E Chambers; Nikita Zubkov; Markéta Kubánková; Jonathon Nixon-Abell; Ioanna Mela; Susana Abreu; Max Schwiening; Giulia Lavarda; Ismael López-Duarte; Jennifer A Dickens; Tomás Torres; Clemens F Kaminski; Liam J Holt; Edward Avezov; James A Huntington; Peter St George-Hyslop; Marina K Kuimova; Stefan J Marciniak
Journal:  Sci Adv       Date:  2022-04-08       Impact factor: 14.957

4.  Liver disease in adults with α1-antitrypsin deficiency.

Authors:  Mattias Mandorfer; Theresa Bucsics; Veronika Hutya; Karin Schmid-Scherzer; Benedikt Schaefer; Heinz Zoller; Arnulf Ferlitsch; Markus Peck-Radosavljevic; Michael Trauner; Peter Ferenci; Meinhard Kneussl; Thomas Reiberger
Journal:  United European Gastroenterol J       Date:  2018-02-28       Impact factor: 4.623

  4 in total

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