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参与细胞外基质周转和血管生成的特定基因的遗传多态性与表达水平与年龄相关性黄斑变性风险的关联分析。

Association analysis of genetic polymorphisms and expression levels of selected genes involved in extracellular matrix turnover and angiogenesis with the risk of age-related macular degeneration.

作者信息

Oszajca Katarzyna, Szemraj Maciej, Szemraj Janusz, Jurowski Piotr

机构信息

a Department of Medical Biochemistry , Medical University of Lodz , Lodz , Poland.

b Department of Ophthalmology and Visual Rehabilitation , Central Veterans' Hospital , Lodz , Poland.

出版信息

Ophthalmic Genet. 2018 Dec;39(6):684-698. doi: 10.1080/13816810.2018.1525752. Epub 2018 Oct 5.

Abstract

BACKGROUND

Age-related macular degeneration is a progressive eye disease affecting the macula and causing acute visual loss particularly in elder people. The aim of the study was an attempt to discern an influence of expression levels and functional genetic polymorphisms of selected genes related to the extracellular matrix turnover or neovascularization on age-related macular degeneration occurrence and progression.

METHODS

We conducted a case-control study of 200 polish patients with recognized age-related macular degeneration (dry and wet) and compared the results with those obtained from matched 100 healthy control subjects. TaqMan Genotyping Assays were employed to examine the following single nucleotide polymorphisms: matrix metalloproteinase (MMP)-2 -735C/T, MMP-7 -181A/G, MMP-9 -1702T/A, and -1562C/T; tissue inhibitors of metalloproteinase (TIMP)-2 -418G/C; vascular endothelial growth factor (VEGF) +405 G/C and +936 C/T, VEGFR-2 +1719 T/A and -271 G/A. Real-time polymerase chain reaction was assessed to determine the mRNA quantity. Serum levels of proteins were measured using enzyme-linked immunosorbent assay.

RESULTS

The single nucleotide polymorphism genotyping showed that TT genotype for MMP-9 -1702T/A and CC genotype for VEGF +936C/T increase markedly the risk of age-related macular degeneration but do not influence on its progression. Additionally, the possible protective effect of CC genetic variant in MMP-9 -1562C/T polymorphism against progression of age-related macular degeneration was observed. We also found significant differences in systemic expression levels of MMP-2, -7, -9, TIMP-2, vascular endothelial growth factor, VEGFR-2, and pigment epithelium-derived factor between studied group. The research demonstrated evident differences in serum levels of MMP-2, -7, -9, TIMP-2, vascular endothelial growth factor, and pigment epithelium-derived factor between wet and dry age-related macular degeneration patients.

CONCLUSIONS

We can conclude that disturbances in angiogenic homeostasis and processes of extracellular matrix turnover occurring in age-related macular degeneration-affected ocular tissues may be reflected in changes in systemic expression levels of the investigated genes.

摘要

背景

年龄相关性黄斑变性是一种进行性眼病,影响黄斑并导致急性视力丧失,尤其在老年人中。本研究的目的是试图识别与细胞外基质周转或新生血管形成相关的特定基因的表达水平和功能性基因多态性对年龄相关性黄斑变性发生和进展的影响。

方法

我们对200名确诊为年龄相关性黄斑变性(干性和湿性)的波兰患者进行了病例对照研究,并将结果与100名匹配的健康对照受试者的结果进行比较。采用TaqMan基因分型检测法检测以下单核苷酸多态性:基质金属蛋白酶(MMP)-2 -735C/T、MMP-7 -181A/G、MMP-9 -1702T/A和-1562C/T;金属蛋白酶组织抑制剂(TIMP)-2 -418G/C;血管内皮生长因子(VEGF)+405 G/C和+936 C/T,血管内皮生长因子受体-2(VEGFR-2)+1719 T/A和-271 G/A。采用实时聚合酶链反应评估来确定mRNA数量。使用酶联免疫吸附测定法测量血清蛋白水平。

结果

单核苷酸多态性基因分型显示,MMP-9 -1702T/A的TT基因型和VEGF +936C/T的CC基因型显著增加年龄相关性黄斑变性的风险,但不影响其进展。此外,观察到MMP-9 -1562C/T多态性中的CC基因变异对年龄相关性黄斑变性进展可能具有保护作用。我们还发现研究组之间MMP-2、-7、-9、TIMP-2、血管内皮生长因子、VEGFR-2和色素上皮衍生因子的全身表达水平存在显著差异。该研究表明湿性和干性年龄相关性黄斑变性患者之间血清中MMP-2、-7、-9、TIMP-2、血管内皮生长因子和色素上皮衍生因子水平存在明显差异。

结论

我们可以得出结论,年龄相关性黄斑变性受累眼组织中发生的血管生成稳态紊乱和细胞外基质周转过程可能反映在所研究基因的全身表达水平变化中。

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