首页> 外文期刊>European journal of ophthalmology >Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population
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Lack of association between lysyl oxidase-like 1 polymorphism in pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population

机译:北印度人口伪萃取综合征和伪萃取青光眼缺乏溶酶氧化酶样1多态性之间的关联

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摘要

Introduction: Pseudoexfoliation syndrome is commonly associated with pseudoexfoliation glaucoma. The two nonsynonymous single-nucleotide polymorphisms rs1048661 (R141L) and rs3825942 (G153D) within exon 1 of LOXL1 gene have been found to confer risk of pseudoexfoliation syndrome and pseudoexfoliation glaucoma in different geographical populations. This study aims to find association between two nonsynonymous single-nucleotide polymorphisms with pseudoexfoliation syndrome and pseudoexfoliation glaucoma in North Indian population. Methods: North Indian subjects clinically diagnosed with pseudoexfoliation syndrome/pseudoexfoliation glaucoma and normal age-matched control were enrolled in the study. Genomic DNA was extracted and the two single-nucleotide polymorphisms of LOXL1 gene were genotyped by polymerase chain reaction and sequencing. The association between single-nucleotide polymorphisms with pseudoexfoliation syndrome/pseudoexfoliation glaucoma was evaluated by chi-square test. Results: A total of 30 pseudoexfoliation glaucoma, 27 pseudoexfoliation syndrome and 61 control subjects were enrolled in the study. Patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma did not show any genetic association with either single-nucleotide polymorphism rs1048661 or rs3825942. Conclusion: The study shows lack of association between LOXL1 single-nucleotide polymorphisms and pseudoexfoliation in North Indian population.
机译:介绍:伪掺杂综合征通常与伪炼金糖有关。已经发现,在LOX11基因的外显子1内,在LOX11基因的外显子1内的两个非纯单核苷酸多态性RS1048661(R1411)和RS3825942(G153D)赋予不同地理群体伪萃取综合征和伪萃取荧光眼的风险。本研究旨在在北印度人口伪萃取综合征和伪萃取青光眼之间找到两个非纯单核苷酸多态性之间的关联。方法:北方印度受试者临床诊断为伪掺杂综合征/假冒掺杂青光眼和正常年龄匹配的对照。提取基因组DNA,并通过聚合酶链反应和测序进行LOX11基因的两种单核苷酸多态性。通过Chi-Square试验评估了用伪萃取综合征/假杀症青光眼的单核苷酸多态性之间的关联。结果:共有30名伪挑解的青光眼,27例伪掺杂综合征和61项对照受试者进行了研究。伪掺杂综合征和伪萃取青光眼的患者没有显示出与单核苷酸多态性RS1048661或RS3825942的任何遗传结合。结论:该研究表明,北印度人群缺乏LOXL1单核苷酸多态性和伪拔出之间的关联。

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