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  1. Article ; Online: Penetrance, cancer incidence and survival in HFE haemochromatosis-A population-based cohort study.

    Schaefer, Benedikt / Pammer, Lorenz M / Pfeifer, Bernhard / Neururer, Sabrina / Troppmair, Maria R / Panzer, Marlene / Wagner, Sonja / Pertler, Elke / Gieger, Christian / Kronenberg, Florian / Lamina, Claudia / Tilg, Herbert / Zoller, Heinz

    Liver international : official journal of the International Association for the Study of the Liver

    2024  Volume 44, Issue 3, Page(s) 838–847

    Abstract: Background and aims: Haemochromatosis is characterized by progressive iron overload affecting the liver and can cause cirrhosis and hepatocellular carcinoma. Most haemochromatosis patients are homozygous for p.C282Y in HFE, but only a minority of ... ...

    Abstract Background and aims: Haemochromatosis is characterized by progressive iron overload affecting the liver and can cause cirrhosis and hepatocellular carcinoma. Most haemochromatosis patients are homozygous for p.C282Y in HFE, but only a minority of individuals with this genotype will develop the disease. The aim was to assess the penetrance of iron overload, fibrosis, hepatocellular carcinoma and life expectancy.
    Methods: A total of 8839 individuals from the Austrian region of Tyrol were genotyped for the p.C282Y variant between 1997 and 2021. Demographic, laboratory parameters and causes of death were assessed from health records. Penetrance, survival, and cancer incidence were ascertained from diagnosed cases, insurance- and cancer registry data. Outcomes were compared with a propensity score-matched control population.
    Results: Median age at diagnosis in 542 p.C282Y homozygous individuals was 47.8 years (64% male). At genotyping, the prevalence of iron overload was 55%. The cumulative penetrance of haemochromatosis defined as the presence of provisional iron overload was 24.2% in males and 10.5% in females aged 60 years or younger. Among p.C282Y homozygotes of the same ages, the cumulative proportion of individuals without fibrosis (FIB-4 score < 1.3) was 92.8% in males and 96.7% in females. Median life expectancy was reduced by 6.8 years in individuals homozygous for p.C282Y when compared with population-matched controls (p = .001). Hepatocellular carcinoma incidence was not significantly higher in p.C282Y homozygotes than in controls matched for age and sex.
    Conclusion: Reduced survival and the observed age-dependent increase in penetrance among p.C282Y homozygotes call for earlier diagnosis of haemochromatosis to prevent complications.
    MeSH term(s) Female ; Humans ; Male ; Middle Aged ; Hemochromatosis/epidemiology ; Hemochromatosis/genetics ; Hemochromatosis/complications ; Penetrance ; Carcinoma, Hepatocellular/epidemiology ; Carcinoma, Hepatocellular/genetics ; Carcinoma, Hepatocellular/complications ; Cohort Studies ; Incidence ; Histocompatibility Antigens Class I/genetics ; Hemochromatosis Protein/genetics ; Iron Overload/complications ; Homozygote ; Liver Cirrhosis/complications ; Liver Neoplasms/epidemiology ; Liver Neoplasms/genetics ; Liver Neoplasms/complications ; Mutation
    Chemical Substances Histocompatibility Antigens Class I ; Hemochromatosis Protein ; HFE protein, human
    Language English
    Publishing date 2024-01-23
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2102783-3
    ISSN 1478-3231 ; 1478-3223
    ISSN (online) 1478-3231
    ISSN 1478-3223
    DOI 10.1111/liv.15797
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Impact of preoperative anemia, iron-deficiency and inflammation on survival after colorectal surgery-A retrospective cohort study.

    Bath, Messina / Viveiros, André / Schaefer, Benedikt / Klein, Sebastian / Pammer, Lorenz M / Wagner, Sonja / Lorenz, Andreas / Rugg, Christopher / Gasser, Elisabeth / Ninkovic, Marijana / Panzer, Marlene / Pertler, Elke / Fries, Dietmar / Tilg, Herbert / Weiss, Guenter / Petzer, Verena / Öfner-Velano, Dietmar / Zoller, Heinz

    PloS one

    2022  Volume 17, Issue 7, Page(s) e0269309

    Abstract: Background: Anemia is present in up to two-thirds of patients undergoing colorectal surgery mainly caused by iron deficiency and inflammation. As anemia is associated with increased risk of perioperative death, diagnosis and treatment of preoperative ... ...

    Abstract Background: Anemia is present in up to two-thirds of patients undergoing colorectal surgery mainly caused by iron deficiency and inflammation. As anemia is associated with increased risk of perioperative death, diagnosis and treatment of preoperative anemia according to etiology have been recommended.
    Objective: The aim of the present study was to assess if the association between anemia and survival in patients undergoing colorectal surgery was determined by the severity of anemia alone or also by anemia etiology.
    Methods: To determine the prevalence of anemia and etiology, preoperative hematological parameters, C-reactive protein, ferritin and transferrin saturation were retrospectively assessed and correlated with outcome in a cohort of patients undergoing colorectal surgery between 2005 and 2019 at the University Hospital of Innsbruck. Anemia was defined as hemoglobin <120 g/L in females and <130 g/L in males. The etiology of anemia was classified on the basis of serum iron parameters, as iron deficiency anemia, anemia of inflammation or other anemia etiologies.
    Results: Preoperative anemia was present in 54% (1316/2458) of all patients. Anemia was associated with iron deficiency in 45% (134/299) and classified as anemia of inflammation in 32% (97/299) of patients with available serum iron parameters. The etiology of anemia was a strong and independent predictor of survival, where iron deficiency and anemia of inflammation were associated with better postoperative survival than other anemia etiologies. One year survival rates were 84.3%, 77.3% and 69.1% for patients with iron deficiency anemia, anemia of inflammation and other anemia types. Inflammation indicated by high C-reactive protein is a strong negative predictor of overall survival.
    Conclusions: Anemia has a high prevalence among patients undergoing colorectal surgery and rational treatment requires early assessment of serum iron parameters and C-reactive protein.
    MeSH term(s) Anemia/complications ; Anemia/epidemiology ; Anemia, Iron-Deficiency/complications ; Anemia, Iron-Deficiency/epidemiology ; C-Reactive Protein/metabolism ; Cohort Studies ; Colorectal Surgery ; Female ; Hemoglobins/metabolism ; Humans ; Inflammation ; Iron ; Iron Deficiencies ; Male ; Retrospective Studies
    Chemical Substances Hemoglobins ; C-Reactive Protein (9007-41-4) ; Iron (E1UOL152H7)
    Language English
    Publishing date 2022-07-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0269309
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Synonymous mutation in adenosine triphosphatase copper-transporting beta causes enhanced exon skipping in Wilson disease.

    Panzer, Marlene / Viveiros, André / Schaefer, Benedikt / Baumgartner, Nadja / Seppi, Klaus / Djamshidian, Atbin / Todorov, Theodor / Griffiths, William J H / Schott, Eckart / Schuelke, Markus / Eurich, Dennis / Stättermayer, Albert Friedrich / Bomford, Adrian / Foskett, Pierre / Vodopiutz, Julia / Stauber, Rudolf / Pertler, Elke / Morell, Bernhard / Tilg, Herbert /
    Müller, Thomas / Kiechl, Stefan / Jimenez-Heredia, Raul / Weiss, Karl Heinz / Hahn, Si Houn / Janecke, Andreas / Ferenci, Peter / Zoller, Heinz

    Hepatology communications

    2022  Volume 6, Issue 7, Page(s) 1611–1619

    Abstract: Wilson disease (WD) is caused by biallelic pathogenic variants in adenosine triphosphatase copper-transporting beta (ATP7B); however, genetic testing identifies only one or no pathogenic ATP7B variant in a number of patients with WD. Synonymous single- ... ...

    Abstract Wilson disease (WD) is caused by biallelic pathogenic variants in adenosine triphosphatase copper-transporting beta (ATP7B); however, genetic testing identifies only one or no pathogenic ATP7B variant in a number of patients with WD. Synonymous single-nucleotide sequence variants have been recognized as pathogenic in individual families. The aim of the present study was to evaluate the prevalence and disease mechanism of the synonymous variant c.2292C>T (p.Phe764=) in WD. A cohort of 280 patients with WD heterozygous for a single ATP7B variant was investigated for the presence of c.2292C>T (p.Phe764=). In this cohort of otherwise genetically unexplained WD, the allele frequency of c.2292C>T (p.Phe764=) was 2.5% (14 of 560) compared to 7.1 × 10
    MeSH term(s) Copper/metabolism ; Copper-Transporting ATPases/genetics ; Exons/genetics ; Hepatolenticular Degeneration/genetics ; Humans ; Mutation/genetics ; Silent Mutation
    Chemical Substances Copper (789U1901C5) ; Copper-Transporting ATPases (EC 7.2.2.8)
    Language English
    Publishing date 2022-03-10
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2471-254X
    ISSN (online) 2471-254X
    DOI 10.1002/hep4.1922
    Database MEDical Literature Analysis and Retrieval System OnLINE

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