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首页> 外文期刊>British journal of ophthalmology >Plasma homocysteine, methylene tetrahydrofolate reductase C677T and factor II G20210A polymorphisms, factor VIII, and VWF in central retinal vein occlusion.
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Plasma homocysteine, methylene tetrahydrofolate reductase C677T and factor II G20210A polymorphisms, factor VIII, and VWF in central retinal vein occlusion.

机译:视网膜中央静脉阻塞中血浆同型半胱氨酸,亚甲基四氢叶酸还原酶C677T和因子II G20210A多态性,因子VIII和VWF。

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AIMS: To determine whether plasma homocysteine, methylene tetrahydrofolate reductase (MTHFR) C677T and factor II G20210A polymorphisms, factor VIII, and vWF are risk factors for central retinal vein occlusion (CRVO). METHOD: Prospective comparison of 63 consecutive patients with central retinal vein occlusion and 63 age matched controls. Plasma homocysteine and vWF were estimated by ELISA, the MTFHR and factor II G20210A polymorphisms determined by polymerase chain reaction with restriction enzyme product digestion and factor VIII by one stage automated clotting assay. RESULTS: Plasma homocysteine (patients: median 12.4 micromol/l, controls: median 11.6 micromol OR = 1.05, p=0.20), factor VIII (patients: median = 115 U/dl, controls: median = 113 U/dl), and vWF (patients: median = 115 U/dl, controls: median = 108 U/dl) were not statistically higher in patients than in controls. Five CRVO patients and seven controls were homozygous for the MTHFR C677T mutation. One control was heterozygous for the factor II G20210A mutation. CONCLUSION: This study has not identified new risk factors for CRVO.
机译:目的:为了确定血浆高半胱氨酸,亚甲基四氢叶酸还原酶(MTHFR)C677T和因子II G20210A多态性,因子VIII和vWF是否是视网膜中央静脉阻塞(CRVO)的危险因素。方法:对63例连续性视网膜中央静脉阻塞患者和63例年龄相匹配的对照者进行前瞻性比较。通过ELISA估计血浆高半胱氨酸和vWF,通过限制性内切酶产物消化和因子VIII的聚合酶链反应通过一级自动凝血测定法测定MTFHR和因子II G20210A多态性。结果:血浆同型半胱氨酸(患者:中位数12.4微摩尔/升,对照组:中位数11.6微摩尔OR = 1.05,p = 0.20),凝血因子VIII(患者:中位数= 115 U / dl,对照组:中位数= 113 U / dl)和患者的vWF(患者:中位数= 115 U / dl,对照组:中位数= 108 U / dl)在统计学上不高于对照组。 5名CRVO患者和7名对照为MTHFR C677T突变纯合子。一个对照是因子II G20210A突变的杂合子。结论:本研究尚未发现CRVO的新危险因素。

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