Mossbock Georg, Weger Martin, Faschinger Christoph, Steinbrugger Iris, Temmel Werner, Schmut Otto, Renner Wilfried, Hufnagel Clemens, Stanger Olaf
University Clinic for Ophthalmology, Medical University of Graz, Graz, Austria.
Mol Vis. 2006 Apr 17;12:356-9.
Increased plasma homocysteine levels have been found in patients with primary open angle glaucoma (POAG) and glaucoma secondary to pseudoexfoliation syndrome (PEXG). A common polymorphism of the methylenetetrahydrofolatereductase (MTHFR 677C>T) leads to moderately elevated plasma homocysteine levels particularly under conditions of impaired folate status. It was the aim of this study to investigate a hypothesized association between this polymorphism and the presence of either POAG or PEXG.
The present retrospective case-control study included a total of 553 participants comprising 204 patients with POAG, 138 patients with PEXG, and 211 control subjects. Genotyping for the MTHFR 677C>T polymorphism was performed by polymerase chain reaction (PCR).
No significant difference in the genotype distribution of the MTHFR 677C>T polymorphism was found between control subjects and patients with POAG or PEXG. The prevalence of the MTHFR 677TT genotype was 6.9% in patients with POAG, 11.6% in patients with PEXG, and 9.5% in control subjects.
The present data suggest that the MTHFR 677C>T polymorphism itself is not a major genetic risk factor for POAG and PEXG in a central European population.
在原发性开角型青光眼(POAG)和假性剥脱综合征(PEXG)继发的青光眼患者中发现血浆同型半胱氨酸水平升高。亚甲基四氢叶酸还原酶(MTHFR 677C>T)的常见多态性会导致血浆同型半胱氨酸水平适度升高,尤其是在叶酸状态受损的情况下。本研究的目的是调查这种多态性与POAG或PEXG的存在之间的假设关联。
本回顾性病例对照研究共纳入553名参与者,包括204例POAG患者、138例PEXG患者和211名对照者。通过聚合酶链反应(PCR)对MTHFR 677C>T多态性进行基因分型。
在对照者与POAG或PEXG患者之间,未发现MTHFR 677C>T多态性的基因型分布有显著差异。MTHFR 677TT基因型在POAG患者中的患病率为6.9%,在PEXG患者中为11.6%,在对照者中为9.5%。
目前的数据表明,在中欧人群中,MTHFR 677C>T多态性本身并非POAG和PEXG的主要遗传危险因素。