Markers of thrombophilia in retinal vein thrombosis

被引:29
作者
Hansen, L
Kristensen, HL
Bek, T
Ingerslev, J
机构
[1] Aarhus Univ Hosp, Dept Ophthalmol, DK-8000 Aarhus, Denmark
[2] Aarhus Univ Hosp, Dept Clin Immunol, DK-8000 Aarhus, Denmark
[3] Aarhus Univ Hosp, Ctr Haemophilia & Thrombosis, DK-8000 Aarhus, Denmark
来源
ACTA OPHTHALMOLOGICA SCANDINAVICA | 2000年 / 78卷 / 05期
关键词
retinal vein thrombosis; hyperhomocysteinemia; risk factor; genetic abnormalities;
D O I
10.1034/j.1600-0420.2000.078005523.x
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To study the prevalence of risk factors for systemic thromboembolism in patients with retinal vein thrombosis (RVT), Methods: Fifty-four patients younger than 70 years, diagnosed with a retinal vein thrombosis at the Department of Ophthalmology, Arhus University Hospital, were examined for the presence of venous thrombosis risk factors. Results: 23 patients had a central RVT, 26 had a branch RVT, and 4 had a macular RVT Nineteen (35.2%) of the patients displayed increased levels of plasma homocysteine, one patient (1.9%) the Factor V Leiden mutation, and one patient (1.9%) displayed an antiphospholipid antibody. All other tests for thrombophilia rendered normal. In 15 of the patients with hyperhomocysteinemia, folic acid substitution returned plasma homocysteine to a normal value in 12 cases. Conclusion: A surprisingly high prevalence of hyperhomocysteinemia was detected in this cohort of RVT patients, clearly superseding the prevalence of around 17% found in patients suffering venous thromboembolism in other vascular compartments. Our finding points to the likelihood that hyperhomocysteinemia may be a significant risk factor for retinal vein thrombosis.
引用
收藏
页码:523 / 526
页数:4
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