Screening for hemochromatosis in asymptomatic subjects with or without a family history

Lawrie W. Powell*, Jeannette L. Dixon, Grant A. Ramm, David M. Purdie, Douglas J. Lincoln, Gregory J. Anderson, V. Nathan Subramaniam, David G. Hewett, Jeffrey W. Searle, Linda M. Fletcher, Darrell H. Crawford, Helen Rodgers, Katrina J. Allen, Juleen A. Cavanaugh, Mark L. Bassett

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    169 Citations (Scopus)

    Abstract

    Background: Hemochromatosis in white subjects is mostly due to homozygosity for the common C282Y substitution in HFE. Although clinical symptoms are preventable by early detection of the genetic predisposition and prophylactic treatment, population screening is not currently advocated because of the discrepancy between the common mutation prevalence and apparently lower frequency of clinical disease. This study compared screening for hemochromatosis in subjects with or without a family history. Methods: We assessed disease expression by clinical evaluation and liver biopsy in 672 essentially asymptomatic C282Y homozygous subjects identified by either family screening or health checks. We also observed a subgroup of untreated homozygotes with normal serum ferritin levels for up to 24 years. Results: Prevalence of hepatic iron overload and fibrosis were comparable between the 2 groups. Diseaserelated conditions were more common in male subjects identified by health checks, but they were older. Hepatic iron overload (grades 2-4) was present in 56% and 34.5% of male and female subjects, respectively; hepatic fibrosis (stages 2-4) in 18.4% and 5.4%; and cirrhosis in 5.6% and 1.9%. Hepatic fibrosis and cirrhosis correlated significantly with the hepatic iron concentration, and except in cases of cirrhosis, there was a 7.5-fold reduction in the mean fibrosis score after phlebotomy. All subjects with cirrhosis were asymptomatic. Conclusions: Screening for hemochromatosis in apparently healthy subjects homozygous for the C282Y mutation with or without a family history reveals comparable levels of hepatic iron overload and disease. Significant hepatic fibrosis is frequently found in asymptomatic subjects with hemochromatosis and, except when cirrhosis is present, is reversed by iron removal.

    Original languageEnglish
    Pages (from-to)294-301
    Number of pages8
    JournalArchives of Internal Medicine
    Volume166
    Issue number3
    DOIs
    Publication statusPublished - 13 Feb 2006

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