The significance of haemochromatosis gene mutations in the general population: implications for screening
M J Burt
a Department of Medicine, b Department of Pathology, Christchurch Hospital, Christchurch,
New Zealand
Correspondence to: Dr M J Burt, Department of
Gastroenterology, Christchurch Hospital, Christchurch, New Zealand. Accepted for publication 7 July 1998 Background Keywords:
haemochromatosis;
iron overload;
HFE
gene;
screening
Haemochromatosis is associated with
mutations in the HFE gene but the significance of these
mutations in the general population is unknown.
Aims
To determine the frequency of
HFE gene mutations in the general population, their effect
on serum iron indexes, and their role in screening for haemochromatosis.
Methods
Deoxyribonucleic acid (DNA) from 1064 randomly selected subjects was analysed for the C282Y and H63D
mutations in the HFE gene. Serum iron, transferrin
saturation, and ferritin were measured and individuals with increased
iron indexes were investigated to confirm or exclude a clinical
diagnosis of haemochromatosis.
Results
Mutations were identified in 409 individuals (38.4%) with heterozygote (carrier) frequencies of 13.2%
and 24.3% for the C282Y and H63D mutations respectively.
Heterozygosity for either mutation significantly increased serum iron
and transferrin saturation but despite a similar trend for ferritin,
this was only significant for C282Y homozygotes. Five individuals
(0.47%) were homozygous for the C282Y mutation, three of whom had
haemochromatosis confirmed by liver biopsy (0.28%). The other two
C282Y homozygotes would not have been detected by phenotypic screening alone.
Conclusions
HFE mutations are
present in 38.4% of the population, affect serum iron indexes, and are
important determinants of iron status. The population frequency of
genetically defined haemochromatosis (C282Y homozygosity) is
approximately one in 200 and is higher than the prevalence of
clinically apparent haemochromatosis.
(GUT 1998;43:830-836)
© 1998 by Gut
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