首页> 外国专利> METHOD OF PREDICTING RISK OF DEVELOPING PRIMARY OPEN ANGLE GLAUCOMA IN INDIVIDUALS DEPENDING ON PRESENCE/ABSENCE OF OTHER NON-COMMUNICABLE EYE DISEASES

METHOD OF PREDICTING RISK OF DEVELOPING PRIMARY OPEN ANGLE GLAUCOMA IN INDIVIDUALS DEPENDING ON PRESENCE/ABSENCE OF OTHER NON-COMMUNICABLE EYE DISEASES

机译:预测因其他非传染性眼病的存在/不存在而导致个人原发性开角型青光眼的风险的方法

摘要

FIELD: medicine.;SUBSTANCE: invention relates to medical diagnostics and concerns a method for prediction of risk of developing primary open-angle glaucoma depending on presence/absence of accompanying non-infectious pathology eyes in Russian individuals being natives of central black earth region of Russia. Method involves blood sampling and DNA recovery from peripheral venous blood with the following analysis of polymorphisms-VEGF-A-958C T, IGF-1 c.-1410T C, TGFβ-1 c.-1347T C, IGFR-1 g. 99181663C T. To predict a high risk of developing primary open-angle glaucoma in individuals with no concomitant pathology of non-eye if observing the allele T IGFR-1 or a combination of the allele with VEGF-A with alleles t IGFR-1 or a combination of the allele with VEGF-A with alleles t IGF-1 with alleles t TGFβ-1 or a combination of the allele t VEGF-A with alleles t IGF-1 with alleles with TGFβ-1. Predicted is low risk of POAG in without comorbidity eye genotype CC IGFR-1 and combination of genetic variants t VEGF-A and SS IGF-1. To predict a high risk of developing primary open-angle glaucoma among individuals with accompanying pathology eye if observing a combination of alleles with IGF-1 with with TGFβ-1 or a combination of the allele with VEGF-A with genotype VEHICLE IGF-1 with alleles with TGFβ-1.;EFFECT: predict low risk of this disease in individuals with accompanying pathology eye genotype TT TGFβ-1.;1 cl, 6 dwg
机译:发明领域本发明涉及医学诊断学,并且涉及一种根据在俄罗斯个体中是否伴有非传染性病理性眼的存在/不存在来预测原发性开角型青光眼的风险的方法。俄国。方法涉及血液采样和从外周静脉血中回收DNA并进行以下多态性分析-VEGF-A-958C> T,IGF-1 c.-1410T> C,TGFβ-1c.-1347T> C,IGFR-1 g 。 99181663C>T。如果观察到等位基因T IGFR-1或等位基因与VEGF-A和等位基因t IGFR-1的组合,则可以预测没有非伴有非眼病的个体发生原发性开角型青光眼的高风险等位基因与VEGF-A的等位基因t IGF-1与等位基因tTGFβ-1的组合,或等位基因t VEGF-A与等位基因t IGF-1的等位基因与TGFβ-1的等位基因的组合。预测在没有合并症的眼基因型CC IGFR-1以及遗传变异t VEGF-A和SS IGF-1的情况下发生POAG的风险较低。如果观察具有IGF-1等位基因与TGFβ-1的等位基因结合或具有VEHICLE IGF-1基因型与VEGF-A的等位基因结合,则可预测伴有病理性眼的个体中发生原发性开角型青光眼的高风险TFFβ-1等位基因;效果:预测伴有病理性眼基因TTTGFβ-1的个体患此病的风险低; 1 cl,6 dwg

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