학술논문

HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype‐stratified cohort study of hemochromatosis in Australian women
Document Type
article
Source
Journal of Gastroenterology and Hepatology. 32(4)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Prevention
Liver Disease
Genetics
Aging
Contraception/Reproduction
Hematology
Digestive Diseases
2.1 Biological and endogenous factors
Aetiology
Adult
Aged
Australia
Cohort Studies
Female
Ferritins
Genetic Predisposition to Disease
Genotype
Hemochromatosis
Hemochromatosis Protein
Homozygote
Humans
Menopause
Middle Aged
Mutation
hereditary hemochromatosis
HFE p
C282Y homozygosity
iron accumulation
iron overload-related disease
menopause
women's health
HealthIron Study Investigators
HFE p.C282Y homozygosity
Gastroenterology & Hepatology
Clinical sciences
Language
Abstract
Background and aimWomen who are homozygous for the p.C282Y mutation in the HFE gene are at much lower risk of iron overload-related disease than p.C282Y homozygous men, presumably because of the iron-depleting effects of menstruation and pregnancy. We used data from a population cohort study to model the impact of menstruation cessation at menopause on serum ferritin (SF) levels in female p.C282Y homozygotes, with p.C282Y/p.H63D simple or compound heterozygotes and those with neither p.C282Y nor p.H63D mutations (HFE wild types) as comparison groups.MethodsA sample of the Melbourne Collaborative Cohort Study was selected for the "HealthIron" study (n = 1438) including all HFE p.C282Y homozygotes plus a random sample stratified by HFE-genotype (p.C282Y and p.H63D). The relationship between the natural logarithm of SF and time since menopause was examined using linear mixed models incorporating spline smoothing.ResultsFor p.C282Y homozygotes, SF increased by a factor of 3.6 (95% CI (1.8, 7.0), P