Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion

Citation
J. Larsson et al., Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion, ACT OPHTH S, 78(3), 2000, pp. 340-343
Citations number
39
Categorie Soggetti
Optalmology
Journal title
ACTA OPHTHALMOLOGICA SCANDINAVICA
ISSN journal
13953907 → ACNP
Volume
78
Issue
3
Year of publication
2000
Pages
340 - 343
Database
ISI
SICI code
1395-3907(200006)78:3<340:HATMCM>2.0.ZU;2-F
Abstract
Background: Hyperhomocysteinemia is a factor that predisposes to thrombosis , and the C677T mutation in methylene-tehrahydrofolate reductase (MTHFR) is known to give increased plasma homocysteine, We wanted to investigate if t hese factors were overrepresented in a group of patients with central retin al vein occlusion, Methods: 116 patients with a history of central retinal vein occlusion were examined for the presence of hyperhomocysteinemia and the MTHFR C677T muta tion. Results: Compared to the control groups, there was no significant increase, neither in plasma homocysteine nor in the frequency of the MTHFR C677T mut ation in the patients, Even when we looked selectively at the young patient s, age less than 50 years, no difference could be detected, Conclusion: It seems that neither hyperhomocysteinemia nor the MTHFR C677T mutation is an important risk factor for the aetiology of central retinal v ein occlusion.