Utility of hepatic or total body iron burden in the assessment of advanced hepatic fibrosis in HFE hemochromatosis
Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH, it is important to assess the likelihood of cirrhosis and thus the need for confirmatory liver biopsy. Therapeutic phlebotomy also provides an estimate...
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Published in | Scientific reports Vol. 9; no. 1; pp. 20234 - 8 |
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Abstract | Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH, it is important to assess the likelihood of cirrhosis and thus the need for confirmatory liver biopsy. Therapeutic phlebotomy also provides an estimate of mobilisable iron stores. We determined whether mobilisable iron stores may predict the presence of advanced fibrosis. Retrospective analysis of 137 male and 65 female HH subjects was undertaken. Biochemical, histological and phlebotomy data were available on all subjects. The mean values of HIC, HIC × [age], mobilisable iron, mobilisable iron × [age] and serum ferritin in the cohort were higher in the group with advanced fibrosis. HIC had an optimum sensitivity and specificity of 73% for the diagnosis of advanced liver fibrosis, with a cut-off HIC level of 200 µmol/g (AUROC 0.83, p < 0.0001). AUROC for HIC was greater in females (0.93) than males (0.79). Mobilisable iron had an optimum sensitivity and specificity both of 83% at a cut-off of 9.6 g for the prediction of advanced fibrosis in all subjects (AUROC 0.92, p < 0.0001). Mobilisable iron stores provide a simple, clinically useful indication of the risk of advanced fibrosis and should routinely be considered. |
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AbstractList | Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH, it is important to assess the likelihood of cirrhosis and thus the need for confirmatory liver biopsy. Therapeutic phlebotomy also provides an estimate of mobilisable iron stores. We determined whether mobilisable iron stores may predict the presence of advanced fibrosis. Retrospective analysis of 137 male and 65 female HH subjects was undertaken. Biochemical, histological and phlebotomy data were available on all subjects. The mean values of HIC, HIC × [age], mobilisable iron, mobilisable iron × [age] and serum ferritin in the cohort were higher in the group with advanced fibrosis. HIC had an optimum sensitivity and specificity of 73% for the diagnosis of advanced liver fibrosis, with a cut-off HIC level of 200 µmol/g (AUROC 0.83, p < 0.0001). AUROC for HIC was greater in females (0.93) than males (0.79). Mobilisable iron had an optimum sensitivity and specificity both of 83% at a cut-off of 9.6 g for the prediction of advanced fibrosis in all subjects (AUROC 0.92, p < 0.0001). Mobilisable iron stores provide a simple, clinically useful indication of the risk of advanced fibrosis and should routinely be considered. Abstract Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH, it is important to assess the likelihood of cirrhosis and thus the need for confirmatory liver biopsy. Therapeutic phlebotomy also provides an estimate of mobilisable iron stores. We determined whether mobilisable iron stores may predict the presence of advanced fibrosis. Retrospective analysis of 137 male and 65 female HH subjects was undertaken. Biochemical, histological and phlebotomy data were available on all subjects. The mean values of HIC, HIC × [age], mobilisable iron, mobilisable iron × [age] and serum ferritin in the cohort were higher in the group with advanced fibrosis. HIC had an optimum sensitivity and specificity of 73% for the diagnosis of advanced liver fibrosis, with a cut-off HIC level of 200 µmol/g (AUROC 0.83, p < 0.0001). AUROC for HIC was greater in females (0.93) than males (0.79). Mobilisable iron had an optimum sensitivity and specificity both of 83% at a cut-off of 9.6 g for the prediction of advanced fibrosis in all subjects (AUROC 0.92, p < 0.0001). Mobilisable iron stores provide a simple, clinically useful indication of the risk of advanced fibrosis and should routinely be considered. Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH, it is important to assess the likelihood of cirrhosis and thus the need for confirmatory liver biopsy. Therapeutic phlebotomy also provides an estimate of mobilisable iron stores. We determined whether mobilisable iron stores may predict the presence of advanced fibrosis. Retrospective analysis of 137 male and 65 female HH subjects was undertaken. Biochemical, histological and phlebotomy data were available on all subjects. The mean values of HIC, HIC × [age], mobilisable iron, mobilisable iron × [age] and serum ferritin in the cohort were higher in the group with advanced fibrosis. HIC had an optimum sensitivity and specificity of 73% for the diagnosis of advanced liver fibrosis, with a cut-off HIC level of 200 µmol/g (AUROC 0.83, p < 0.0001). AUROC for HIC was greater in females (0.93) than males (0.79). Mobilisable iron had an optimum sensitivity and specificity both of 83% at a cut-off of 9.6 g for the prediction of advanced fibrosis in all subjects (AUROC 0.92, p < 0.0001). Mobilisable iron stores provide a simple, clinically useful indication of the risk of advanced fibrosis and should routinely be considered.Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH, it is important to assess the likelihood of cirrhosis and thus the need for confirmatory liver biopsy. Therapeutic phlebotomy also provides an estimate of mobilisable iron stores. We determined whether mobilisable iron stores may predict the presence of advanced fibrosis. Retrospective analysis of 137 male and 65 female HH subjects was undertaken. Biochemical, histological and phlebotomy data were available on all subjects. The mean values of HIC, HIC × [age], mobilisable iron, mobilisable iron × [age] and serum ferritin in the cohort were higher in the group with advanced fibrosis. HIC had an optimum sensitivity and specificity of 73% for the diagnosis of advanced liver fibrosis, with a cut-off HIC level of 200 µmol/g (AUROC 0.83, p < 0.0001). AUROC for HIC was greater in females (0.93) than males (0.79). Mobilisable iron had an optimum sensitivity and specificity both of 83% at a cut-off of 9.6 g for the prediction of advanced fibrosis in all subjects (AUROC 0.92, p < 0.0001). Mobilisable iron stores provide a simple, clinically useful indication of the risk of advanced fibrosis and should routinely be considered. |
ArticleNumber | 20234 |
Author | Ramm, Grant A. Olynyk, John K. Chin, Justin Ramm, Louise E. Ayonrinde, Oyekoya T. Powell, Lawrie W. |
Author_xml | – sequence: 1 givenname: Justin surname: Chin fullname: Chin, Justin email: chinjustin@hotmail.com organization: Department of Gastroenterology & Hepatology, Fiona Stanley Fremantle Hospital Group – sequence: 2 givenname: Lawrie W. surname: Powell fullname: Powell, Lawrie W. organization: Faculty of Medicine, The University of Queensland, Herston – sequence: 3 givenname: Louise E. surname: Ramm fullname: Ramm, Louise E. organization: Hepatic Fibrosis Group, QIMR Berghofer Medical Research Institute – sequence: 4 givenname: Oyekoya T. surname: Ayonrinde fullname: Ayonrinde, Oyekoya T. organization: Department of Gastroenterology & Hepatology, Fiona Stanley Fremantle Hospital Group – sequence: 5 givenname: Grant A. surname: Ramm fullname: Ramm, Grant A. organization: Faculty of Medicine, The University of Queensland, Herston, Hepatic Fibrosis Group, QIMR Berghofer Medical Research Institute – sequence: 6 givenname: John K. surname: Olynyk fullname: Olynyk, John K. organization: Department of Gastroenterology & Hepatology, Fiona Stanley Fremantle Hospital Group, School of Medical and Health Sciences, Edith Cowan University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31882912$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1056_NEJMra2119758 crossref_primary_10_20514_2226_6704_2024_14_6_442_456 crossref_primary_10_1016_j_hoc_2022_12_006 crossref_primary_10_1038_s41598_023_35028_4 crossref_primary_10_1016_j_mayocp_2022_02_017 crossref_primary_10_1002_14651858_CD011817_pub2 crossref_primary_10_1007_s12072_023_10510_3 crossref_primary_10_7759_cureus_50043 crossref_primary_10_1016_j_gastha_2024_01_011 crossref_primary_10_1080_03009742_2020_1800081 |
Cites_doi | 10.1002/hep.24330 10.1016/j.gcb.2007.12.021 10.1001/archinte.166.3.294 10.1111/j.1572-0241.2005.41287.x 10.1016/0168-8278(91)90084-O 10.1111/jgh.13621 10.1080/1024533032000158832 10.7326/0003-4819-129-11_Part_2-199812011-00003 10.1002/hep.22650 10.1111/j.1572-0241.2001.03472.x 10.1038/ng0896-399 10.1055/s-0030-1255356 10.1148/radiology.148.3.6878708 10.1111/j.1572-0241.1998.00346.x |
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Snippet | Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH, it is... Abstract Development of advanced hepatic fibrosis in HFE Hemochromatosis (HH) is influenced by hepatic iron concentration (HIC) and age. In patients with HH,... |
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SubjectTerms | 692/4020/4021/1607/1604 692/4020/4021/1607/1605 Adult Biopsy Cirrhosis Female Ferritin Ferritins - blood Fibrosis Genotype Hemochromatosis Hemochromatosis - diagnosis Hemochromatosis - genetics Hemochromatosis - metabolism Hemochromatosis Protein - genetics Hemochromatosis Protein - metabolism Homozygote Humanities and Social Sciences Humans Iron Iron - metabolism Iron Overload - diagnosis Iron Overload - metabolism Liver Liver - metabolism Liver cirrhosis Liver Cirrhosis - diagnosis Liver Cirrhosis - genetics Liver Cirrhosis - metabolism Male Middle Aged multidisciplinary Mutation, Missense Phlebotomy Phlebotomy - methods Retrospective Studies ROC Curve Science |
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Title | Utility of hepatic or total body iron burden in the assessment of advanced hepatic fibrosis in HFE hemochromatosis |
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