年龄相关性黄斑变性和慢性闭角型青光眼增殖综合征的遗传标志物

L. Balashova, N. A. Bakunina, A. Fedorov, Y. Kuznetsova, A. Popov, M. E. Viner
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摘要

目的:对原发性慢性闭角型青光眼(PACG)和年龄相关性黄斑变性(AMD)的临床和遗传学研究,为这些疾病的前瞻性病因导向靶向治疗提供依据。材料和方法。15例孤立性眼增殖综合征患者根据诊断分为2组:1)7例(14眼),年龄55岁至83岁,确诊为湿性AMD患者(4女3男)。2) 慢性PACG患者8例(16眼),年龄45~80岁,其中女性5例,男性3例。随访1~3年。后果在这两种情况下,我们都发现俄罗斯人群中参与增殖过程的基因突变:VEGF A、CFH和COL11A1。我们开发了一种全外显子组/全基因组测序数据的生物信息学分析算法,该算法考虑了临床和遗传数据的总和,有助于改善增殖过程的预后。遗传标记在患者的一生中保持不变,因此在老年进行这些研究很重要。结论为了预防慢性PACG和AMD患者的增殖综合征,并制定针对这些疾病的个体靶向病因治疗方案,需要进行专门的分子遗传学测试,其结果可以用所开发的算法进行分析。
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Genetic markers of the proliferative syndrome in age-related macular degeneration and chronic angle-closure glaucoma
Purpose: clinical and genetic research of primary chronic angle-closure glaucoma (PACG) and age-related macular degeneration (AMD) for prospective pathogenetically-oriented targeted treatment of these condition.Materials and methods. 15 patients with isolated ocular proliferative syndrome were divided into 2 groups depending on their diagnosis: 1) 7 patients (14 eyes) aged 55 to 83 with confirmed wet AMD (4 women and 3 men). 2) 8 patients (16 eyes) aged 45 to 80 with chronic PACG (5 women and 3 men). The patients were followed up for 1 to 3 years.Results. In both conditions, we found mutations in the genes of the Russian population involved in the process of proliferation: VEGF A, CFH, and COL11A1. We developed an algorithm of bioinformatic analysis of full-exome/full-genome sequencing data which takes account of the aggregate of clinical and genetic data and helps refine the prognosis of the course of proliferation. Genetic markers remain unchanged throughout the patient’s life, so it is important to conduct these studies in old age.Conclusion. To prevent the proliferative syndrome in patients with chronic PACG and AMD, and develop individual targeted pathogenetic therapy schemes for these diseases, specialized molecular genetic tests are needed, the results of which could be analyzed with the developed algorithm.
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CiteScore
0.50
自引率
0.00%
发文量
107
审稿时长
16 weeks
期刊最新文献
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