Characterization of polymorphisms in CFI and ARMS genes and their association with exudative age-related macular degeneration in Algerian patients.

IF 1.5 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Biology Research Communications Pub Date : 2022-06-01 DOI:10.22099/mbrc.2022.43634.1743
Ghania Abid, Ahlem Messal, Mohammed Harmel, Aicha Idder, Mostefa Fodil, Faouzia Zemani-Fodil
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引用次数: 2

Abstract

Increasing evidence shows that polymorphisms in CFI and ARMS2 genes can influence exudative age-related macular degeneration (nAMD) risk. The aim of this study was to assess the role of CFI rs10033900 and ARMS2 rs3750846 polymorphisms in susceptibility to nAMD for the first time in the Algerian population. A total of one hundred twenty four controls and seventy two nAMD cases were included in the present study. Genomic DNA was extracted from venous blood leukocytes. CFI rs10033900 and ARMS2 rs3750846 variants were determined by using the real‑time polymerase chain reaction method. Differences in allele and genotype distribution between the cases and controls were tested with adjustment for age by logistic regression analysis. A stratification of case and control groups by age (<65 or ≥65) and by gender (male and female) was also performed. Statistical analyses were done using SPSS21.0. No statistically significant association was observed between CFI rs10033900 and ARMS2 rs3750846 polymorphisms and nAMD risk (p>0.05 for all comparisons). Stratification by age and gender did not show any significant association between these two polymorphisms and nAMD in a sample of the Algerian population. In our study, CFI rs10033900 and ARMS2 rs3750846 polymorphisms did not predispose alone to nAMD in our population. This study is a contribution to the enrichment of the bank data concerning the CFI and ARMS2 genes, reporting, for the first time, the allelic and genotypic frequencies of these genes polymorphisms characterizing the Algerian population.

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阿尔及利亚患者CFI和ARMS基因多态性特征及其与渗出性年龄相关性黄斑变性的关系
越来越多的证据表明,CFI和ARMS2基因的多态性可以影响渗出性年龄相关性黄斑变性(nAMD)的风险。本研究的目的是首次在阿尔及利亚人群中评估CFI rs10033900和ARMS2 rs3750846多态性在nAMD易感性中的作用。本研究共纳入124例对照和72例nAMD病例。从静脉血白细胞中提取基因组DNA。采用实时聚合酶链反应法检测CFI rs10033900和ARMS2 rs3750846变异。病例与对照组的等位基因和基因型分布差异经年龄校正后进行logistic回归分析。按年龄(CFI rs10033900和ARMS2 rs3750846多态性和nAMD风险)对病例组和对照组进行分层(所有比较p>0.05)。在阿尔及利亚人口样本中,年龄和性别分层未显示这两种多态性与nAMD之间有任何显著关联。在我们的研究中,CFI rs10033900和ARMS2 rs3750846多态性在我们的人群中并不单独易患nAMD。这项研究对丰富CFI和ARMS2基因的数据库数据做出了贡献,首次报道了阿尔及利亚人群中这些基因多态性的等位基因和基因型频率。
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来源期刊
Molecular Biology Research Communications
Molecular Biology Research Communications BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.00
自引率
0.00%
发文量
12
期刊介绍: “Molecular Biology Research Communications” (MBRC) is an international journal of Molecular Biology. It is published quarterly by Shiraz University (Iran). The MBRC is a fully peer-reviewed journal. The journal welcomes submission of Original articles, Short communications, Invited review articles, and Letters to the Editor which meets the general criteria of significance and scientific excellence in all fields of “Molecular Biology”.
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