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Investigation of the association between the GLC3A locus and normal tension glaucoma in Japanese patients by microsatellite analysis

机译:日本人GLC3A基因座与正常张力性青光眼的微卫星分析

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Purpose: To investigate whether the GLC3A locus harboring the CYP1B1 gene is associated with normal tension glaucoma (NTG) in Japanese patients.Materials and Methods: One hundred forty-two Japanese patients with NTG and 101 Japanese healthy controls were recruited. Patients exhibiting a comparatively early onset were selected as this suggests that genetic factors may show stronger involvement. Genotyping and assessment of allelic diversity was performed on 13 highly polymorphic microsatellite markers in and around the GLC3A locus.Results: There were decreased frequencies of the 444 allele of D2S0416i and the 258 allele of D2S0425i in cases compared to controls (P = 0.022 and P = 0.034, respectively). However, this statistical significance disappeared when corrected (Pc >?0.05). We did not find any significant association between the remaining 11 microsatellite markers, including D2S177, which may be associated with CYP1B1, and NTG (P >?0.05).Conclusions: Our study showed no association between the GLCA3 locus and NTG, suggesting that the CYP1B1 gene, which is reportedly involved in a range of glaucoma phenotypes, may not be an associated factor in the pathogenesis of NTG.
机译:目的:探讨携带CYP1B1基因的GLC3A基因位点是否与日本正常青光眼(NTG)相关。材料与方法:招募142例日本NTG患者和101名日本健康对照者。选择表现出相对较早发作的患者,因为这表明遗传因素可能显示出更强的参与性。对GLC3A基因座及其周围的13个高度多态性微卫星标记进行了基因分型和等位基因多样性评估。结果:与对照组相比,D2S0416i的444个等位基因和D2S0425i的258个等位基因的频率降低(P = 0.022和P分别为0.034)。但是,校正后,该统计显着性消失了(Pc>?0.05)。我们没有发现剩余的11个微卫星标记之间有任何显着相关性,包括D2S177,可能与CYP1B1和NTG相关(P>?0.05)。结论:我们的研究表明GLCA3基因座和NTG之间没有相关性,提示CYP1B1基因,据报道参与一系列青光眼表型,可能不是NTG发病机制中的相关因素。

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