Suppr超能文献

西班牙塔拉戈纳普通地中海人群中 C282Y、H63D 和 S65C HFE 基因突变、饮食和生活方式因素对铁状态的影响。

Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.

机构信息

IISPV, Universitat Rovira i Virgili, Tarragona, Spain.

出版信息

Ann Hematol. 2010 Aug;89(8):767-73. doi: 10.1007/s00277-010-0901-9. Epub 2010 Jan 28.

Abstract

Mutations in the HFE gene result in iron overload and can produce hereditary hemochromatosis (HH), a disorder of iron metabolism characterized by increased intestinal iron absorption. Dietary quality, alcoholism and other life-style factors can increase the risk of iron overload, especially among genetically at risk populations. Polymorphisms of the HFE gene (C282Y, H63D and S65C) were measured together with serum ferritin (SF), transferrin saturation (TS) and hemoglobin, to measure iron status, in randomly-selected healthy subjects living in the Spanish Mediterranean coast (n = 815; 425 females, 390 males), 18 to 75 years of age. The intake of dietary components that affect iron absorption was calculated from 3-day dietary records. The presence of C282Y/H63D compound heterozygote that had a prevalence of 2.8% in males and 1.2% in females was associated with an elevated TS and SF. No subject was homozygous for C282Y or S65C. The C282Y heterozygote, H63D heterozygote and homozygote and H63D/S65C compound heterozygote genotypes were associated with increased TS relative to the wild type in the general population. These genotypes together with the alcohol and iron intake increase the indicators of iron status, while calcium intake decreases them. We did not observe any affect of the S65C heterozygote genotype on these levels. All the HFE genotypes except for the S65C heterozygote together with the alcohol, iron and calcium intake affect the indicators of iron status. The C282Y/H63D compound heterozygote genotype has the higher phenotypic expression in our Spanish Mediterranean population.

摘要

HFE 基因突变导致铁过载,并可引发遗传性血色素沉着症(HH),这是一种铁代谢紊乱的疾病,其特征是肠道铁吸收增加。饮食质量、酗酒和其他生活方式因素会增加铁过载的风险,尤其是在具有遗传风险的人群中。我们在西班牙地中海沿岸的随机选择的健康受试者(n=815;425 名女性,390 名男性)中,18 至 75 岁,一起测量了 HFE 基因(C282Y、H63D 和 S65C)的多态性和血清铁蛋白(SF)、转铁蛋白饱和度(TS)和血红蛋白,以衡量铁的状态。从 3 天的饮食记录中计算出影响铁吸收的饮食成分的摄入量。C282Y/H63D 复合杂合子的存在率在男性中为 2.8%,在女性中为 1.2%,与 TS 和 SF 升高有关。没有受试者是 C282Y 或 S65C 的纯合子。在一般人群中,C282Y 杂合子、H63D 杂合子和纯合子以及 H63D/S65C 复合杂合子基因型与 TS 升高有关。这些基因型与酒精和铁的摄入一起增加了铁状态的指标,而钙的摄入则降低了这些指标。我们没有观察到 S65C 杂合子基因型对这些水平有任何影响。除了 S65C 杂合子基因型外,所有的 HFE 基因型都与酒精、铁和钙的摄入一起影响铁状态的指标。在我们的西班牙地中海人群中,C282Y/H63D 复合杂合子基因型具有更高的表型表达。

相似文献

2
HFE gene mutations an Apulian population: allele frequencies.
Eur J Epidemiol. 2003;18(7):685-9. doi: 10.1023/a:1024844906872.
3
[Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
Rev Clin Esp. 2002 Oct;202(10):534-9. doi: 10.1016/s0014-2565(02)71137-5.
7
Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.
J Hepatol. 2002 Apr;36(4):474-9. doi: 10.1016/s0168-8278(01)00304-x.
9
Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
Ann Hematol. 2012 Apr;91(4):491-5. doi: 10.1007/s00277-011-1338-5. Epub 2011 Sep 27.
10
HFE mutations, iron deficiency and overload in 10,500 blood donors.
Br J Haematol. 2001 Aug;114(2):474-84. doi: 10.1046/j.1365-2141.2001.02949.x.

引用本文的文献

1
Genetic history of Scythia.
Sci Adv. 2025 Jul 25;11(30):eads8179. doi: 10.1126/sciadv.ads8179. Epub 2025 Jul 23.
2
HFE mutations in patients with iron overload in Santa Catarina: a cross-sectional study.
Sao Paulo Med J. 2025 Jul 4;143(4):e2023359. doi: 10.1590/1516-3180.2023.0359.R1.07032025. eCollection 2025.
6
Hereditary hemochromatosis caused by a C282Y/H63D mutation in the HFE gene: A case report.
Heliyon. 2024 Mar 21;10(7):e28046. doi: 10.1016/j.heliyon.2024.e28046. eCollection 2024 Apr 15.
8
H63D Homozygous Mutation: An Unusual Cause of Deranged Liver Function Test in an Elderly Patient.
Cureus. 2022 Nov 23;14(11):e31840. doi: 10.7759/cureus.31840. eCollection 2022 Nov.
10
C282Y/H63D Compound Heterozygosity Is a Low Penetrance Genotype for Iron Overload-related Disease.
J Can Assoc Gastroenterol. 2022 Jul 28;5(5):240-247. doi: 10.1093/jcag/gwac025. eCollection 2022 Oct.

本文引用的文献

1
HFE gene mutations in patients with altered iron metabolism in Argentina.
Cell Mol Biol (Noisy-le-grand). 2009 Jul 1;55(2):31-5.
3
Extrinsic factors modifying expressivity of the HFE variant C282Y, H63D, S65C phenotypes in 1,294 Danish men.
Ann Hematol. 2009 Oct;88(10):957-65. doi: 10.1007/s00277-009-0714-x. Epub 2009 Mar 7.
4
Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
Ann Hematol. 2009 Aug;88(8):775-84. doi: 10.1007/s00277-008-0679-1. Epub 2009 Jan 22.
5
Iron involvement in multiple signaling pathways of atherosclerosis: a revisited hypothesis.
Curr Med Chem. 2008;15(21):2157-72. doi: 10.2174/092986708785747634.
6
HFE gene mutations, serum ferritin level, transferrin saturation, and their clinical correlates in a Korean population.
Dig Dis Sci. 2009 Apr;54(4):879-86. doi: 10.1007/s10620-008-0432-6. Epub 2008 Aug 6.
8
Iron storage disease: facts, fiction and progress.
Blood Cells Mol Dis. 2007 Sep-Oct;39(2):140-7. doi: 10.1016/j.bcmd.2007.03.009. Epub 2007 May 31.
9
Regulation of systemic iron homeostasis: how the body responds to changes in iron demand.
Biometals. 2007 Jun;20(3-4):665-74. doi: 10.1007/s10534-006-9030-2. Epub 2007 Feb 2.
10
Iron bioavailability: UK Food Standards Agency workshop report.
Br J Nutr. 2006 Nov;96(5):985-90. doi: 10.1017/bjn20061894.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验