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Evaluation of the association between five genetic variants and primary open-angle glaucoma in a Han Chinese population.评价五个遗传变异与汉族人群原发性开角型青光眼的关联。
Ophthalmic Genet. 2020 Jun;41(3):252-256. doi: 10.1080/13816810.2020.1747089. Epub 2020 Apr 13.
2
Association of the SIX6 locus with primary open angle glaucoma in southern Chinese and Japanese.SIX6 基因座与中国南方和日本原发性开角型青光眼的相关性研究。
Exp Eye Res. 2019 Mar;180:129-136. doi: 10.1016/j.exer.2018.12.014. Epub 2018 Dec 23.
3
Down-regulated miR-187 promotes oxidative stress-induced retinal cell apoptosis through P2X7 receptor.下调的 miR-187 通过 P2X7 受体促进氧化应激诱导的视网膜细胞凋亡。
Int J Biol Macromol. 2018 Dec;120(Pt A):801-810. doi: 10.1016/j.ijbiomac.2018.08.166. Epub 2018 Aug 28.
4
MicroRNA-related polymorphisms in pseudoexfoliation syndrome, pseudoexfoliative glaucoma, and primary open-angle glaucoma.假性剥脱综合征、假性剥脱性青光眼和原发性开角型青光眼中与微小RNA相关的多态性
Ophthalmic Genet. 2018 Oct;39(5):603-609. doi: 10.1080/13816810.2018.1509352. Epub 2018 Aug 27.
5
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma.全基因组关联研究鉴定出原发性开角型青光眼的 7 个新的易感位点。
Hum Mol Genet. 2018 Apr 15;27(8):1486-1496. doi: 10.1093/hmg/ddy053.
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A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma.一项针对与原发性开角型青光眼相关的微小RNA相关基因变异的全基因组扫描。
Invest Ophthalmol Vis Sci. 2017 Oct 1;58(12):5368-5377. doi: 10.1167/iovs.17-22410.
7
Genetics of glaucoma.青光眼的遗传学
Hum Mol Genet. 2017 Aug 1;26(R1):R21-R27. doi: 10.1093/hmg/ddx184.
8
Confirmation of involvement of new variants at CDKN2A/B in pediatric acute lymphoblastic leukemia susceptibility in the Spanish population.CDKN2A/B基因新变异与西班牙人群儿童急性淋巴细胞白血病易感性相关性的确证
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9
CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma.CDKN2B基因rs1063192多态性降低青光眼风险。
Oncotarget. 2017 Mar 28;8(13):21167-21176. doi: 10.18632/oncotarget.15504.
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MicroRNA‑93 is overexpressed and induces apoptosis in glaucoma trabecular meshwork cells.微小RNA-93在青光眼小梁网细胞中过表达并诱导细胞凋亡。
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miR182 和 CDKN2B 基因多态性分析在希腊原发性开角型青光眼患者中的研究。

Polymorphism analysis of miR182 and CDKN2B genes in Greek patients with primary open angle glaucoma.

机构信息

1st Department of Ophthalmology, "G. Gennimatas" General Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Department of Ophthalmology, "Evangelismos" General Hospital, Athens, Greece.

出版信息

PLoS One. 2020 Jun 3;15(6):e0233692. doi: 10.1371/journal.pone.0233692. eCollection 2020.

DOI:10.1371/journal.pone.0233692
PMID:32492046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7269255/
Abstract

Glaucoma is a progressive optic neuropathy resulting from retinal ganglion cells death; it represents one of the leading causes of irreversible blindness worldwide. Although, primary open angle glaucoma (POAG) is the most common type of the disease, the pathogenesis of POAG and the genetic factors contributing to disease development remain poorly understood. The aim of this study was to investigate whether the polymorphisms rs76481776 in miR182 gene and rs3217992 in cyclin-dependent kinase inhibitor-2B (CDKN2B) gene are risk factors for POAG in a series of patients of Greek origin. A case-control study was conducted including 120 patients with POAG and 113 unaffected healthy controls of Greek origin, surveyed for polymorphisms with potential correlation to POAG. DNA from each individual was tested for the miR182 rs76481776 and CDKN2B rs3217992 polymorphisms. Regarding the miR182 rs76481776 polymorphism, the T allele occurred with significantly higher frequency in POAG patients compared to controls (OR: 2.62, 95% CI: 1.56-4.39; p = 0.0002). The CDKN2B rs3217992 A allele frequency was found significantly increased in POAG patients compared to healthy individuals (OR: 1.72, 95% CI: 1.18-2.49; p = 0.005). Therefore, both rs76481776 polymorphism in miR182 gene and rs3217992 polymorphism in CDKN2B gene seem to be associated with the development of POAG in a Greek population. The carriers of the T allele of rs76481776 in miR182 and the carriers of the A allele of rs3217992 in CDKN2B have an increased risk of developing POAG.

摘要

青光眼是一种进行性视神经病变,由视网膜神经节细胞死亡引起;它是全球致盲的主要原因之一。虽然原发性开角型青光眼(POAG)是最常见的疾病类型,但 POAG 的发病机制和导致疾病发展的遗传因素仍知之甚少。本研究旨在调查 miR182 基因中的 rs76481776 多态性和细胞周期蛋白依赖性激酶抑制剂-2B(CDKN2B)基因中的 rs3217992 多态性是否是希腊裔患者 POAG 的危险因素。进行了一项病例对照研究,包括 120 名 POAG 患者和 113 名无 POAG 的希腊裔健康对照者,调查了与 POAG 相关的潜在相关性的多态性。对每位个体的 DNA 进行了 miR182 rs76481776 和 CDKN2B rs3217992 多态性检测。关于 miR182 rs76481776 多态性,与对照组相比,POAG 患者的 T 等位基因发生频率明显更高(OR:2.62,95%CI:1.56-4.39;p = 0.0002)。与健康个体相比,POAG 患者的 CDKN2B rs3217992 A 等位基因频率明显升高(OR:1.72,95%CI:1.18-2.49;p = 0.005)。因此,miR182 基因中的 rs76481776 多态性和 CDKN2B 基因中的 rs3217992 多态性似乎与希腊人群 POAG 的发生有关。miR182 中的 rs76481776 等位基因的 T 携带者和 CDKN2B 中的 rs3217992 等位基因的 A 携带者发生 POAG 的风险增加。