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晚期非渗出性年龄相关性黄斑变性中的肿瘤坏死因子基因多态性

Tumor Necrosis Factor Gene Polymorphisms in Advanced Non-exudative Age-related Macular Degeneration.

作者信息

Bonyadi Mohammad Hossein Jabbarpoor, Bonyadi Morteza, Ahmadieh Hamid, Fotuhi Nikoo, Shoeibi Nasser, Saadat Saeed, Yagubi Zakieh

机构信息

Department of Ophthalmology, Gonabad University of Medical Sciences, Gonabad, Iran ; Center of Excellence for Biodiversity, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.

Center of Excellence for Biodiversity, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.

出版信息

J Ophthalmic Vis Res. 2015 Apr-Jun;10(2):155-9. doi: 10.4103/2008-322X.163781.

DOI:10.4103/2008-322X.163781
PMID:26425318
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4568613/
Abstract

PURPOSE

To investigate tumor necrosis factor (TNF)-α gene polymorphisms in advanced dry-type age-related macular degeneration (AMD) in a population from Northeastern Iran.

METHODS

In this case-control study, 50 patients with geographic macular atrophy and 73 gender-matched controls were enrolled. Genomic deoxyribonucleic acid (DNA) was extracted from the peripheral blood. Polymerase chain reaction was performed to analyze 2 candidate single nucleotide polymorphisms in the TNF-α gene, namely -1031 thymine (T)/cytosine (C) and -308 guanine (G)/adenine (A).

RESULTS

The distribution of the - 1031 T/C genotype was TT, 62%; TC, 36%; CC, 2% in the patients and TT, 60%; TC, 36%; CC, 4% in the controls (P = 0.94). Genotype analysis of TNF-α -308 also revealed no significant difference in distribution between patients (G, 78%; GA, 22%; AA, 0%) and controls (GG, 74%; GA, 23%; AA, 3%) (P = 0.51). None of the haplotypes nor alleles of studied TNF-α polymorphisms were significantly associated with advanced dry-type AMD.

CONCLUSION

The findings of this study show that polymorphisms in the TNF-α gene, do not play an important role in dry-type AMD in the studied population.

摘要

目的

在伊朗东北部人群中研究晚期干性年龄相关性黄斑变性(AMD)患者的肿瘤坏死因子(TNF)-α基因多态性。

方法

在这项病例对照研究中,纳入了50例地图状黄斑萎缩患者和73例性别匹配的对照者。从外周血中提取基因组脱氧核糖核酸(DNA)。采用聚合酶链反应分析TNF-α基因中的2个候选单核苷酸多态性,即-1031位胸腺嘧啶(T)/胞嘧啶(C)和-308位鸟嘌呤(G)/腺嘌呤(A)。

结果

患者中-1031 T/C基因型的分布为TT,62%;TC,36%;CC,2%;对照者中TT,60%;TC,36%;CC,4%(P = 0.94)。TNF-α -308的基因型分析也显示,患者(G,78%;GA,22%;AA,0%)和对照者(GG,74%;GA,23%;AA,3%)之间的分布无显著差异(P = 0.51)。所研究的TNF-α多态性的单倍型和等位基因均与晚期干性AMD无显著关联。

结论

本研究结果表明,TNF-α基因多态性在该研究人群的干性AMD中不发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74c/4568613/6a9431ce650a/JOVR-10-155-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74c/4568613/7f0d2fa2fd7a/JOVR-10-155-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74c/4568613/6a9431ce650a/JOVR-10-155-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74c/4568613/7f0d2fa2fd7a/JOVR-10-155-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74c/4568613/6a9431ce650a/JOVR-10-155-g002.jpg

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