Activated protein C resistance in anterior ischaemic optic neuropathy

被引:16
作者
Nagy, V
Facsko, A
Takacs, L
Balazs, E
Berta, A
Balogh, I
Edes, I
Czuriga, I
Pfliegler, G
机构
[1] Univ Debrecen, Fac Med, Dept Ophthalmol, Med & Hlth Sci Ctr, H-4012 Debrecen, Hungary
[2] Univ Debrecen, Dept Clin Biochem & Mol Pathol, Med & Hlth Sci Ctr, H-4012 Debrecen, Hungary
[3] Univ Debrecen, Dept Cardiol, Med & Hlth Sci Ctr, H-4012 Debrecen, Hungary
[4] Univ Debrecen, Div Rare Dis, Med & Hlth Sci Ctr, H-4012 Debrecen, Hungary
来源
ACTA OPHTHALMOLOGICA SCANDINAVICA | 2004年 / 82卷 / 02期
关键词
activated protein C resistance; Leiden mutation; non-arteritic anterior ischaemic optic neuropathy;
D O I
10.1111/j.1600-0420.2004.00226.x
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: Protein C is a major component of the natural anticoagulant pathway. Resistance of coagulation factor V (FV) to activated protein C (APC), mostly due to FV Leiden mutation, is the most common cause of inherited thrombophilia. The aim of this retrospective study was to determine the prevalence of APC resistance and Leiden mutation in patients with non-arteritic anterior ischaemic optic neuropathy (NAION). Methods: A total of 25 patients with NAION were examined between 1997 and 2002. The patients were screened for APC resistance and FV Leiden mutation as well as for acquired risk factors of vascular disease such as diabetes mellitus, hypercholesterolaemia, hypertonia and ischaemic heart disease. A control group of subjects without ocular vascular disease and with homogenous distribution of the same risk factors was used for comparison. Results: Six of the 25 patients (24%) with NAION had APC resistance due to the heterozygous Leiden mutation of FV. The frequency of the same genetic mutation in the control group was only 5.9%. Odds ratio calculations showed that patients with the Leiden mutation were at a significantly higher risk of NAION than control patients (p less than or equal to 0.021). Conclusion: The high frequency of Leiden mutation in NAION suggests a pathogenic role of the mutation in the disease.
引用
收藏
页码:140 / 143
页数:4
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