PATHOGENETICALLY DIRECTED METHOD OF PREVENTION AND TREATMENT OF AGE-MACULAR DEGENERATION

Y. Saldan, Y. Panchenko, N. Malachkova
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Abstract

Background. Age-related macular degeneration is one of the most common causes of blindness in developed countries, especially in people over 60 years old. The incidence of AMD is projected to increase to 288 million in 2040 compared to 196 million in 2020. Cardiovascular factors, smoking, alcohol consumption, overweight, genetic factors, and metabolic disorders are risk factors for the development of AMD. There are disorders of lipid metabolism, as well as hyperreactivity of platelet purine receptors may be associated with the progression of AMD. The AREDS2 formula is currently used to treat AMD. New therapeutic strategies aimed to correct metabolic disorders are needed to decrease the development of the late stages of AMD. Aim: to investigate the effectiveness of improving pathogenetically directed method of prevention and treatment of age-related macular degeneration. Materials and methods. We observed 40 patients (80 eyes), aged 50-85 years, with AMD of category 3 (intermediate AMD), who were divided into 2 groups. The main group included 20 patients (40 eyes), 14 women and 6 men, who have prescribed a complex drug according to the standard AREDS2 scheme, as well as fenofibrate (200 mg) and clopidogrel bisulfate (75 mg). The control group included 20 patients (40 eyes), 13 women and 7 men. These patients received AREDS2 standard treatment. Progression was evaluated according to the results of OCT of the macular area according to the AREDS classification and control of corrected visual acuity (CVA). The observation period was 2 years. Results. No signs of progression were noted in patients of both observation groups within 6 months from the start of the prescribed therapy. In the patients of the control group, the progression of the disease was recorded after 1 year of observation according to both defined criteria. Changes in OCT were observed in 7,5% of patients in the control group, and a decrease in CVA- in 5%. In the patients of the main group who used the extended therapeutic regimen, after 1 year of follow-up, progression according to OCT signs was noted in 2,5% of cases, but there was no worsening of CVA. After 2 years of observation, signs of progression according to OST were recorded in the main group by 50% less than in the control group. According to CVA, disease progression was detected in 15% of the main group and 30% of the control group. Conclusions. This study complemented already existing therapeutic strategies for the preventive treatment of AMD.
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老年性黄斑变性的病理学防治方法
背景。年龄相关性黄斑变性是发达国家最常见的致盲原因之一,特别是在60岁以上的人群中。AMD的发病率预计将从2020年的1.96亿增加到2040年的2.88亿。心血管因素、吸烟、饮酒、超重、遗传因素和代谢紊乱是AMD发生的危险因素。脂质代谢紊乱以及血小板嘌呤受体的高反应性可能与AMD的进展有关。AREDS2配方目前用于治疗AMD。需要新的治疗策略来纠正代谢紊乱,以减少AMD晚期的发展。目的:探讨改进病理指导方法防治老年性黄斑变性的效果。材料和方法。我们观察了40例(80眼),年龄50 ~ 85岁,AMD为3型(中度),分为两组。主要组包括20例患者(40只眼),14名女性和6名男性,他们根据标准AREDS2方案开了一种复合药物,以及非诺贝特(200毫克)和硫酸氯吡格雷(75毫克)。对照组患者20例(40眼),女性13例,男性7例。这些患者接受了AREDS2标准治疗。按照AREDS矫正视力分级与控制标准(CVA),根据黄斑区OCT检查结果评价进展情况。观察期2年。结果。在处方治疗开始后的6个月内,两组患者均未发现进展迹象。对照组患者在观察1年后,根据两种标准记录疾病的进展情况。对照组中有7.5%的患者OCT改变,5%的患者CVA-下降。在采用延长治疗方案的主要组患者中,随访1年后,2.5%的病例根据OCT体征出现进展,但CVA没有恶化。经过2年的观察,根据OST记录的进展迹象,主组比对照组少50%。根据CVA, 15%的主组和30%的对照组检测到疾病进展。结论。本研究补充了已有的AMD预防性治疗策略。
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审稿时长
7 weeks
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