Literature DB >> 2066547

Biochemical liver profile in hemochromatosis. A survey of 100 patients.

E Lin1, P C Adams.   

Abstract

To determine the frequency of liver profile abnormalities in hereditary hemochromatosis, we under took a retrospective survey in 100 patients, all of whom had undergone liver biopsy. Liver histology was compared with the biochemical profile, which included aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase, bilirubin and albumin determinations. Mild abnormalities in the AST and ALT levels were seen in more than 65% of patients. Patients with cirrhosis had significantly greater elevations in AST, ALT, and alkaline phosphatase, and a significant decrease in albumin (p less than 0.05). Proband cases had more frequent abnormalities than discovered cases within families. Accordingly, we find that mild abnormalities in the biochemical liver profile are common in hemochromatosis and suggest that patients with an unexplained abnormality in the liver profile should be screened for hemochromatosis with a serum ferritin and transferrin saturation.

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Year:  1991        PMID: 2066547     DOI: 10.1097/00004836-199106000-00013

Source DB:  PubMed          Journal:  J Clin Gastroenterol        ISSN: 0192-0790            Impact factor:   3.062


  8 in total

1.  Probability of C282Y homozygosity decreases as liver transaminase activities increase in participants with hyperferritinemia in the hemochromatosis and iron overload screening study.

Authors:  Paul C Adams; Mark Speechley; James C Barton; Christine E McLaren; Gordon D McLaren; John H Eckfeldt
Journal:  Hepatology       Date:  2012-04-18       Impact factor: 17.425

2.  The diversity of liver diseases among outpatient referrals for an elevated serum ferritin.

Authors:  Karen Wong; Paul C Adams
Journal:  Can J Gastroenterol       Date:  2006-07       Impact factor: 3.522

Review 3.  The myths and realities of hemochromatosis.

Authors:  Melanie D Beaton; Paul C Adams
Journal:  Can J Gastroenterol       Date:  2007-02       Impact factor: 3.522

4.  Screening for genetic haemochromatosis in blood samples with raised alanine aminotransferase.

Authors:  M Bhavnani; D Lloyd; A Bhattacharyya; J Marples; P Elton; M Worwood
Journal:  Gut       Date:  2000-05       Impact factor: 23.059

5.  Individuals homozygous for the H63D mutation have significantly elevated iron indexes.

Authors:  Jason Samarasena; Wendy Winsor; Richard Lush; Peter Duggan; Yagang Xie; Mark Borgaonkar
Journal:  Dig Dis Sci       Date:  2006-04       Impact factor: 3.199

6.  GNPAT p.D519G is independently associated with markedly increased iron stores in HFE p.C282Y homozygotes.

Authors:  James C Barton; Wen-Pin Chen; Mary J Emond; Pradyumna D Phatak; V Nathan Subramaniam; Paul C Adams; Lyle C Gurrin; Gregory J Anderson; Grant A Ramm; Lawrie W Powell; Katrina J Allen; John D Phillips; Charles J Parker; Gordon D McLaren; Christine E McLaren
Journal:  Blood Cells Mol Dis       Date:  2016-11-12       Impact factor: 3.039

Review 7.  Abnormal liver enzymes: A review for clinicians.

Authors:  M Ammar Kalas; Luis Chavez; Monica Leon; Pahnwat Tonya Taweesedt; Salim Surani
Journal:  World J Hepatol       Date:  2021-11-27

8.  An efficient machine learning-based approach for screening individuals at risk of hereditary haemochromatosis.

Authors:  Patricia Martins Conde; Thomas Sauter; Thanh-Phuong Nguyen
Journal:  Sci Rep       Date:  2020-11-26       Impact factor: 4.379

  8 in total

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