Mutations in the hemochromatosis gene (HFE) and multiple sclerosis

被引:20
作者
Ristic, S
Lovrecic, L
Brajenovic-Milic, B
Starevic-Cizmarevic, N
Jazbec, SS
Sepcic, J
Kapovic, M
Peterlin, B
机构
[1] Univ Rijeka, Sch Med, Dept Biol & Med Genet, Rijeka 51000, Croatia
[2] UMC, Dept Med Genet, Ljubljana, Slovenia
[3] UMC, Dept Neurol, Ljubljana, Slovenia
[4] Univ Rijeka, Sch Med, Postgrad Study, Rijeka 51000, Croatia
关键词
multiple sclerosis; hemochromatosis; HFE polymorphism; susceptibility gene;
D O I
10.1016/j.neulet.2005.04.045
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the present study we have investigated whether HFE gene polymorphism may play a role in the disease process of Croatian and Slovenian MS patients and their potential genetic susceptibility to MS. We genotyped 314 MS patients and 400 healthy controls for the C282Y and H63D mutations by polymerase chain reaction/restriction fragment length polymorphism (PCR-RFLP) analysis. Our results showed no significant differences in the distribution of the two mutations between MS patients and controls, suggesting that HFE polymorphisms do not contribute to the susceptibility to MS. Also, there was no significant correlation between HFE polymorphism and the disease progression index. However, we observed that MS patients carrying the mutant C282Y allele exhibited earlier onset of disease symptom relative to other genotypes, but it warrants further study in a larger series of MS patients. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:301 / 304
页数:4
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