The Mystery of Glaucoma 2011
DOI: 10.5772/18506
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Homocysteine in the Pathogenesis of Chronic Glaucoma

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Cited by 3 publications
(5 citation statements)
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References 90 publications
(78 reference statements)
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“…There are studies implying that genetic polymorphism, such as variant MTHFR A1298C, may increase the risk for developing glaucoma, especially in the heterozygote model [ 9 , 22 ]. However, in order to support this idea, extended studies are still necessary [ 7 ].…”
Section: Discussionmentioning
confidence: 99%
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“…There are studies implying that genetic polymorphism, such as variant MTHFR A1298C, may increase the risk for developing glaucoma, especially in the heterozygote model [ 9 , 22 ]. However, in order to support this idea, extended studies are still necessary [ 7 ].…”
Section: Discussionmentioning
confidence: 99%
“…Polymorphism in the MTHFR gene may decrease the activity of methylenetetrahydrofolate reductase, leading to a mild increase of homocysteine in the blood [ 7 ]. This may cause problems within blood vessels and is considered a risk factor for thromboembolism.…”
Section: Genetic Features On Retinal Vein Occlusionmentioning
confidence: 99%
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“…10 Pada glaukoma bisa terjadi peningkatan kadar homosistein 11 dan perlu digunakan suplementasi vitamin B1 dan B12 dalam menurunkan kadar homosistein tersebut. 12 Beberapa penelitian lain menemukan bahwa antioksidan seperti vitamin B1 dan B12 memiliki khasiat yang sedikit bahkan tidak berkhasiat sama sekali sebagai terapi untuk penyakit glaukoma. 13 Vitamin B1, atau Tiamin dilaporkan tidak memiliki efek terapi pada IOP (intraocular pressure) yang merupakan faktor resiko utama glauakoma.…”
Section: Metode Penelitianunclassified