Disease-Related Conditions in Relatives of Patients with Hemochromatosis
Zaneta J. Bulaj, M.D., Richard S. Ajioka, Ph.D., John D. Phillips, Ph.D., Bernard A. LaSalle, B.S., Lynn B. Jorde, Ph.D., Linda M. Griffen, B.A., Corwin Q. Edwards, M.D., and James P. Kushner, M.D.
Background Hemochromatosis occurs in approximately 5 white peopleper 1000 and is usually due to homozygosity for mutations inthe HLA-linked HFE gene. Although screening has been proposed,the proportion of homozygotes with conditions related to hemochromatosisis uncertain.
Methods We studied the prevalence of disease-related conditionsamong relatives of probands with hemochromatosis. We identifiedprobands who presented to a clinic with signs or symptoms ofhemochromatosis or who had elevated transferrin-saturation values.We identified homozygous relatives, mainly siblings, on thebasis of HLA identity with the proband and by HFE genotyping.Disease-related conditions were cirrhosis, hepatic fibrosis,elevated aminotransferase values, and hemochromatotic arthropathy.
Results We identified 214 homozygous relatives of 291 homozygousprobands. Of the 113 men in this group (mean age, 41 years),96 (85 percent) had iron overload, and 43 (38 percent) had atleast one disease-related condition. Of the 52 men over 40 yearsof age, 27 (52 percent) had at least one disease-related condition.Of the 101 female homozygous relatives (mean age, 44 years),69 (68 percent) had iron overload, and 10 (10 percent) had atleast one disease-related condition. Of the 43 women over 50years of age, 7 (16 percent) had at least one disease-relatedcondition. If the proband had a disease-related condition, relativeswho were men were more likely to have morbidity than if theproband had no disease-related condition.
Conclusions A substantial number of homozygous relatives ofpatients with hemochromatosis more commonly men thanwomen have conditions related to hemochromatosis thathave yet to be detected clinically.
Source Information
From the Departments of Medicine (Z.J.B., R.S.A., J.D.P., C.Q.E., J.P.K.) and Human Genetics (L.B.J.) and the General Clinical Research Center (B.A.L., L.M.G.), University of Utah School of Medicine; and the LDS Hospital (C.Q.E.) all in Salt Lake City.
Address reprint requests to Dr. Kushner at the Division of Hematology, 4C-416, University of Utah School of Medicine, 50 North Medical Dr., Salt Lake City, UT 84132, or at james.kushner{at}hsc.utah.edu.
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