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热不稳定型亚甲基四氢叶酸还原酶(MTHFR)基因型与视网膜血管阻塞性疾病

Thermolabile MTHFR genotype and retinal vascular occlusive disease.

作者信息

Cahill M, Karabatzaki M, Donoghue C, Meleady R, Mynett-Johnson L A, Mooney D, Graham I M, Whitehead A S, Shields D C

机构信息

The Research Foundation, The Royal Victoria Eye and Ear Hospital, Dublin 2, Ireland. mark.cahill@joslin,harvard.edu

出版信息

Br J Ophthalmol. 2001 Jan;85(1):88-90. doi: 10.1136/bjo.85.1.88.

Abstract

BACKGROUND

Raised levels of total plasma homocysteine (tHcy) are associated with an increased risk of retinal vascular occlusive disease. A thermolabile form of a pivotal enzyme in homocysteine metabolism, methylenetetrahydrofolate reductase (MTHFR), has been associated with vascular occlusive disease and raised tHcy levels. The relation between thermolabile MTHFR genotype, tHcy, and retinal vascular occlusive disease has not been determined.

METHODS

A retrospective case-control study involving hospital based controls and cases with retinal vascular occlusions in whom tHcy levels had been determined was undertaken. Genotyping for the MTHFR 677 C-T mutation that specifies the thermolabile form of the enzyme was performed by established methods in all subjects. The relation between homozygosity for thermolabile MTHFR genotype (TT), raised tHcy levels, and risk of retinal vascular occlusive disease was examined.

RESULTS

87 cases of retinal vascular occlusive disease (mean age 68.7 years) comprising 26 cases of retinal artery occlusion and 61 of retinal vein occlusion were compared with 87 controls (mean age 70.2 years). The TT genotype did not confer a significantly increased risk of retinal vascular occlusive disease. The mean tHcy level was significantly higher in the cases than in the controls (p<0.0001). Overall, and in both the cases and controls, the frequency of the TT genotype was higher in those with normal tHcy levels than in those with increased levels of tHcy. However, the TT genotype did not significantly alter the risk of increased tHcy levels in these patients.

CONCLUSIONS

The TT genotype is not associated with an increased risk of retinal vascular occlusive disease or increased tHcy levels in this group of elderly patients. In older patients, nutritional rather than genetic factors may be more important in increasing tHcy levels, a known risk factor for retinal vascular occlusive disease.

摘要

背景

血浆总同型半胱氨酸(tHcy)水平升高与视网膜血管闭塞性疾病风险增加相关。同型半胱氨酸代谢中的一种关键酶——亚甲基四氢叶酸还原酶(MTHFR)的热不稳定形式,已与血管闭塞性疾病及升高的tHcy水平相关。热不稳定MTHFR基因型、tHcy与视网膜血管闭塞性疾病之间的关系尚未确定。

方法

开展一项回顾性病例对照研究,纳入以医院为基础的对照人群以及已测定tHcy水平的视网膜血管闭塞患者。采用既定方法对所有受试者进行MTHFR 677 C-T突变基因分型,该突变决定了该酶的热不稳定形式。研究热不稳定MTHFR基因型纯合子(TT)、升高的tHcy水平与视网膜血管闭塞性疾病风险之间的关系。

结果

将87例视网膜血管闭塞性疾病患者(平均年龄68.7岁,包括26例视网膜动脉阻塞和61例视网膜静脉阻塞)与87名对照者(平均年龄70.2岁)进行比较。TT基因型并未使视网膜血管闭塞性疾病风险显著增加。病例组的平均tHcy水平显著高于对照组(p<0.0001)。总体而言,在病例组和对照组中,tHcy水平正常者的TT基因型频率均高于tHcy水平升高者。然而,TT基因型并未显著改变这些患者tHcy水平升高的风险。

结论

在这组老年患者中,TT基因型与视网膜血管闭塞性疾病风险增加或tHcy水平升高无关。在老年患者中,营养因素而非遗传因素可能在升高tHcy水平方面更为重要,而tHcy水平升高是视网膜血管闭塞性疾病的一个已知风险因素。

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本文引用的文献

1
Raised plasma homocysteine as a risk factor for retinal vascular occlusive disease.
Br J Ophthalmol. 2000 Feb;84(2):154-7. doi: 10.1136/bjo.84.2.154.
2
Retinal vein occlusion associated with methylenetetrahydrofolate reductase mutation.
Ophthalmology. 1999 Sep;106(9):1817-20. doi: 10.1016/S0161-6420(99)90357-3.
5
Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases.
Atherosclerosis. 1999 Mar;143(1):163-70. doi: 10.1016/s0021-9150(98)00271-8.
9
Homocysteine and atherothrombosis.
N Engl J Med. 1998 Apr 9;338(15):1042-50. doi: 10.1056/NEJM199804093381507.

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