HTRA丝氨酸肽酶1、血管内皮生长因子А、肿瘤坏死因子基因多态性在湿性年龄相关性黄斑变性治疗中的作用

N. Malachkova, O. Al-Jarrah
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They received anti-VEGF A therapy in the form of injections of aflibercept monthly for half a year. Structural changes of the eyes were studied using optical coherence tomography (OCT); polymerase chain reaction (PCR) studies were performed using a Bio-Rad CFX 96 apparatus (BioRad, USA) using a reagent package (Lytech, Russia). Statistical analysis of the obtained results was performed using a set of software packages Statistica 10 (StatSoft, Inc., USA) and SPSS 23.0. Results. It was revealed best prognostic significance in patients with the TC rs2010963 genotype of the VEGFA gene was registered during the analysis of OCT 2 (RR=2.7; 95% CI 1.556 – 4.8), OCT 4 (RR=2.9 ; 95% CI 1.7 – 5.03) and OCT 8 (RR=2.6; 95% CI 1.6 – 4.12) sections, while in patients with the CC genotype these indicators in the OCT 2 section were: RR= 6.1; 95% CI 3.66 – 10.27; in OCT zone 4 RR=4.9; 95% CI 2.9 – 8.29, and in the OCT section 8: RR=4.23; 95% CI 2.7 – 6.556, which indicates a more pronounced influence of the CC genotype. When analyzing rs1800629 of the TNF gene, the best prognostic significance of the GA genotype was established in the OCT 4 (RR=1.77; 95% CI 1.218 – 2.56) and OCT 8 (RR=1.9; 95% CI 1.17 – 3.175) areas (p-value less than 0.05), with the AA genotype in OCT 4 (RR=3.77; 95% CI 2.17 – 6.58), OCT 8 (RR=3.1; 95% CI 1 .7 – 5.59) zones and when evaluating changes in visual acuity of patients with wet AMD (RR=4.2; 95% CI 2 – 8.98). 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Structural changes of the eyes were studied using optical coherence tomography (OCT); polymerase chain reaction (PCR) studies were performed using a Bio-Rad CFX 96 apparatus (BioRad, USA) using a reagent package (Lytech, Russia). Statistical analysis of the obtained results was performed using a set of software packages Statistica 10 (StatSoft, Inc., USA) and SPSS 23.0. Results. It was revealed best prognostic significance in patients with the TC rs2010963 genotype of the VEGFA gene was registered during the analysis of OCT 2 (RR=2.7; 95% CI 1.556 – 4.8), OCT 4 (RR=2.9 ; 95% CI 1.7 – 5.03) and OCT 8 (RR=2.6; 95% CI 1.6 – 4.12) sections, while in patients with the CC genotype these indicators in the OCT 2 section were: RR= 6.1; 95% CI 3.66 – 10.27; in OCT zone 4 RR=4.9; 95% CI 2.9 – 8.29, and in the OCT section 8: RR=4.23; 95% CI 2.7 – 6.556, which indicates a more pronounced influence of the CC genotype. 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引用次数: 0

摘要

介绍。老年性视网膜黄斑变性(AMD)仍被认为是老年人视力丧失的主要原因。该疾病的多因素性影响了现代AMD治疗方法的临床有效性。然而,研究单核苷酸多态性,特别是HtrA丝氨酸肽酶1 (HTRA1)、血管内皮生长因子A (VEGF A)和肿瘤坏死因子(TNF)的发生,是改善和制定更有效的治疗策略的一个有希望的环节。研究的目的。探讨HTRA 1、VEGF A和TNF基因多态性在湿性年龄相关性黄斑变性治疗中的作用。材料与方法:162例湿性AMD患者参与调查。他们接受了抗vegf A治疗,每月注射阿伯西普,持续半年。使用光学相干断层扫描(OCT)研究眼睛的结构变化;聚合酶链反应(PCR)研究使用Bio-Rad CFX 96装置(BioRad,美国)和试剂包(Lytech,俄罗斯)进行。使用Statistica 10 (StatSoft, Inc., USA)和SPSS 23.0软件包对所得结果进行统计分析。结果。在OCT 2分析中发现,VEGFA基因的TC rs2010963基因型患者的预后具有最佳意义(RR=2.7;95% ci 1.556 - 4.8), 10月4日(rr =2.9;95% CI 1.7 - 5.03)和OCT 8 (RR=2.6;95% CI 1.6 - 4.12)切片,而CC基因型患者OCT 2切片的这些指标为:RR= 6.1;95% ci 3.66 - 10.27;OCT 4区RR=4.9;95% CI 2.9 - 8.29,在OCT切片8:RR=4.23;95% CI 2.7 - 6.556,表明CC基因型的影响更为显著。在分析TNF基因rs1800629时,GA基因型在OCT 4中具有最佳的预后意义(RR=1.77;95% CI 1.218 - 2.56)和OCT 8 (RR=1.9;95% CI 1.17 ~ 3.175)区(p值< 0.05),OCT 4为AA基因型(RR=3.77;95% ci 2.17 - 6.58), 10月8日(rr =3.1;95% CI为1.7 - 5.59),当评估湿性AMD患者的视力变化时(RR=4.2;95% ci 2 - 8.98)。HTRA1基因rs11200638的评价结果无统计学意义(p值大于0.05)。结论。我们的研究数据表明血管内皮生长因子a (rs2010963)和肿瘤坏死因子(rs1800629)多态性对阿布利塞普耐药的出现有直接影响。然而,在HtrA丝氨酸肽酶1基因rs11200638存在的情况下,这种影响的研究需要进一步的研究。
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The Role Of HTRA Serine Peptidase 1, Vascular Endothelial Growth Factor А, Tumor Necrosis Factor Gene Polymorphisms in the Treatment Of Wet Age-Related Macular Degeneration
Introduction. Age-related macular degeneration (AMD) of the retina is still considered the leading cause of vision loss in the elderly. The multifactoriality of the disease impairs the clinical effectiveness of modern AMD treatment methods. however, the study of single-nucleotide polymorphisms, in particular, of the HtrA serine peptidase 1 (HTRA1), vascular endothelial growth factor A (VEGF A) and tumor necrosis factor (TNF) genesis a promising link on the way to improve and develope more effective treatment strategies of the disease. The Aim of the Study. To investigate role of HTRA 1, VEGF A and TNF gene polymorphisms in the treatment of wet age-related macular degeneration. Materials and Methods. 162 people with diagnosed wet AMD took part in the investigation. They received anti-VEGF A therapy in the form of injections of aflibercept monthly for half a year. Structural changes of the eyes were studied using optical coherence tomography (OCT); polymerase chain reaction (PCR) studies were performed using a Bio-Rad CFX 96 apparatus (BioRad, USA) using a reagent package (Lytech, Russia). Statistical analysis of the obtained results was performed using a set of software packages Statistica 10 (StatSoft, Inc., USA) and SPSS 23.0. Results. It was revealed best prognostic significance in patients with the TC rs2010963 genotype of the VEGFA gene was registered during the analysis of OCT 2 (RR=2.7; 95% CI 1.556 – 4.8), OCT 4 (RR=2.9 ; 95% CI 1.7 – 5.03) and OCT 8 (RR=2.6; 95% CI 1.6 – 4.12) sections, while in patients with the CC genotype these indicators in the OCT 2 section were: RR= 6.1; 95% CI 3.66 – 10.27; in OCT zone 4 RR=4.9; 95% CI 2.9 – 8.29, and in the OCT section 8: RR=4.23; 95% CI 2.7 – 6.556, which indicates a more pronounced influence of the CC genotype. When analyzing rs1800629 of the TNF gene, the best prognostic significance of the GA genotype was established in the OCT 4 (RR=1.77; 95% CI 1.218 – 2.56) and OCT 8 (RR=1.9; 95% CI 1.17 – 3.175) areas (p-value less than 0.05), with the AA genotype in OCT 4 (RR=3.77; 95% CI 2.17 – 6.58), OCT 8 (RR=3.1; 95% CI 1 .7 – 5.59) zones and when evaluating changes in visual acuity of patients with wet AMD (RR=4.2; 95% CI 2 – 8.98). No statistically significant results were found in the evaluation of the HTRA1 gene rs11200638 (p-value more than 0.05). Conclusions. The data obtained in our study indicate a direct influence of the vascular endothelial growth factor A (rs2010963) and tumor necrosis factor (rs1800629) polymorphisms on the emergence of resistance to aflibercept. However, the study of this influence in the presence of the HtrA serine peptidase 1 gene rs11200638 requires further research.
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