Mabuchi Fumihiko, Tang Sa, Kashiwagi Kenji, Yamagata Zentaro, Iijima Hiroyuki, Tsukahara Shigeo
Department of Ophthalmology, Faculty of Medicine, University of Yamanashi, Shimokato, Yamanashi, Japan.
Mol Vis. 2006 Jul 7;12:735-9.
To assess whether or not the c.677C/T and c.1298A/C genetic polymorphisms of the methylenetetrahydrofolate reductase (MTHFR) gene are associated with open angle glaucoma (OAG).
Genomic DNA was examined in a cohort of 131 Japanese patients with normal tension glaucoma (NTG), 133 patients with primary open angle glaucoma (POAG), and 106 control subjects. The mean age at the time of blood sampling was 62.8+/-13.3 years (mean+/-SD) in the patients with NTG, 61.8+/-15.4 years in the patients with POAG, and 65.0+/-10.5 years in the control subjects. MTHFR c.677C/T and c.1298A/C genotype and allele frequencies were determined using pyrosequencing analysis, and the findings were compared between the OAG patients and control subjects. The frequencies of compound MTHFR c.677C/T and c.1298A/C genotypes were also compared between OAG patients and control subjects.
No significant differences were observed (p>0.05, chi2 test or Fisher's exact test) regarding the MTHFR c.677C/T genotype (TT: 14.5%, CT: 44.3%, CC: 41.2% for patients with NTG; TT: 20.3%, CT: 41.4%, CC: 38.3% for patients with POAG; TT: 17.9%, CT: 36.8%, CC: 45.3% for control subjects) and c.1298A/C (CC: 0%, AC: 38.9%, AA: 61.1% for patients with NTG; CC: 2.3%, AC: 32.3%, AA: 65.4% for patients with POAG; CC: 0.9%, AC: 41.5%, AA: 57.6% for control subjects). There were no allele frequencies between the NTG or POAG patients and the control subjects. In addition, no significant differences (p>0.05, chi2 test) were found in the frequencies of the compound MTHFR c.677C/T and c.1298A/C genotypes between the NTG or POAG patients and the control subjects.
The MTHFR c.677C/T and c.1298A/C polymorphisms were not found to be associated with NTG and POAG. Further studies in the different ethnic populations should be performed to elucidate the relationship between MTHFR and OAG.
评估亚甲基四氢叶酸还原酶(MTHFR)基因的c.677C/T和c.1298A/C基因多态性是否与开角型青光眼(OAG)相关。
对131例日本正常眼压性青光眼(NTG)患者、133例原发性开角型青光眼(POAG)患者和106例对照者的基因组DNA进行检测。NTG患者采血时的平均年龄为62.8±13.3岁(均值±标准差),POAG患者为61.8±15.4岁,对照者为65.0±10.5岁。采用焦磷酸测序分析确定MTHFR c.677C/T和c.1298A/C基因型及等位基因频率,并比较OAG患者与对照者的结果。还比较了OAG患者与对照者中MTHFR c.677C/T和c.1298A/C复合基因型的频率。
MTHFR c.677C/T基因型(NTG患者中TT:14.5%,CT:44.3%,CC:41.2%;POAG患者中TT:20.3%,CT:41.4%,CC:38.3%;对照者中TT:17.9%,CT:36.8%,CC:45.3%)和c.1298A/C(NTG患者中CC:0%,AC:38.9%,AA:61.1%;POAG患者中CC:2.3%,AC:32.3%,AA:65.4%;对照者中CC:0.9%,AC:41.5%,AA:57.6%)方面未观察到显著差异(p>0.05,卡方检验或Fisher精确检验)。NTG或POAG患者与对照者之间的等位基因频率无差异。此外,NTG或POAG患者与对照者之间MTHFR c.677C/T和c.1298A/C复合基因型的频率也未发现显著差异(p>0.05,卡方检验)。
未发现MTHFR c.677C/T和c.1298A/C多态性与NTG和POAG相关。应在不同种族人群中进行进一步研究,以阐明MTHFR与OAG之间的关系。