Åfficacy of nutraceutical drug in the intermediate and wet forms of age-related macular degeneration

E. Eskina, A. Belogurova, A. A. Gvetadze, A. S. Smorchkova
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Abstract

The effectiveness of nutraceutical drug containing oxycarotenoids, vitamins and trace elements, aimed at inhibiting the progression of the dry form of age-related macular degeneration (AMD) has been demonstrated in clinical studies.The purpose of this research is to evaluate the effectiveness of long-term use of a nutraceutical drug in reducing the risk of intermediate AMD evolving into wet AMD, and assess whether it is worth using in patients with wet AMD to reduce the average yearly number of intravitreal injections of angiogenesis inhibitors.Materials and methods. In the first part of the study, we monitored 46 patients with intermediate AMD threatening the progression of the disease (those with multiple confluent drusen, drusenoid, pigment epithelium detachment) for a year: some of them received the drug while others had no nutraceutical support. We assessed standard visual functions, as well as reading parameters (on the Salzburg Reading Desk device), spatial frequency contrast sensitivity (SFC) according to the Zebra program, and macular pigment optical density (on the MPOD device). Retina parameters were controlled by photofixation using Kowa and Clarus 500 fundus camera, and by optical coherence tomography with angiography using a Cirrus 5000 Angioplex, Carl Zeiss. The disease was considered to be progressing if signs of neovascular AMD were detected. In the second part of the study, 35 patients with newly diagnosed neovascular AMD were followed up for a year and treated with angiogenesis inhibitors according to the following pattern: three loading injections of aflibercept and then pro re nata. Of two groups of patients with signs of neovascular AMD, one group took a nutraceutical drug (Lutrin, S.C. Rompharm Company S.R.L., Romania). The number of intravitreal injections of aflibercept administered according to indications during the year was estimated.Results. In the first part of the study, patients with intermediate AMD taking the drug showed an increase in MPOD from 0.36 ± 0.11 to 0.45 ± 0.15 (p = 0.05) and a stable state of the retina and visual functions throughout the entire observation period. In 2 patients (12.5 %) who did not take the drug, the disease progressed to a neovascular form. In the second part of the study, the patients taking the drug received an average of 3.4 ± 0.7 intravitreal injections of aflibercept during the year, compared with 5.3 ± 1.2 injections in the control group without nutraceutical support.Conclusion. Nutraceutical drugs are effective in reducing the risk of intermediate AMD evolving into wet AMD, and thus advisable for patients with wet AMD to reduce the average yearly number of intravitreal injections of angiogenesis inhibitors.
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Åfficacy营养药物在中间和湿形式的老年性黄斑变性
含有类胡萝卜素、维生素和微量元素的营养保健药物对抑制干型老年性黄斑变性(AMD)进展的有效性已在临床研究中得到证实。本研究的目的是评估长期使用一种营养药物在降低中度黄斑变性发展为湿性黄斑变性风险方面的有效性,并评估湿性黄斑变性患者是否值得使用这种药物来减少平均每年玻璃体内注射血管生成抑制剂的次数。材料和方法。在研究的第一部分,我们监测了46例有疾病进展威胁的中度AMD患者(多发性合并性drusen, drusenoid,色素上皮脱离)一年:其中一些患者接受药物治疗,而另一些患者没有营养支持。我们评估了标准视觉功能,以及阅读参数(在萨尔茨堡阅读桌设备上),根据Zebra程序的空间频率对比灵敏度(SFC)和黄斑色素光密度(在MPOD设备上)。视网膜参数通过kova和Clarus 500眼底相机的光固定和卡尔蔡司(Carl Zeiss) Cirrus 5000 Angioplex的光学相干断层扫描血管造影来控制。如果检测到新血管性AMD的迹象,则认为该疾病正在进展。在第二部分研究中,我们对35例新诊断的血管性AMD患者进行了为期一年的随访,并按照以下模式进行了血管生成抑制剂的治疗:阿非利西普3次负荷注射,然后再进行复康。在两组有新生血管性AMD症状的患者中,一组服用营养药物(Lutrin, S.C. Rompharm Company S.R.L,罗马尼亚)。估计了年内根据适应症给予阿非利西普玻璃体内注射的次数。在第一部分研究中,中度AMD患者服用该药后,MPOD从0.36±0.11增加到0.45±0.15 (p = 0.05),整个观察期内视网膜和视觉功能处于稳定状态。在2例(12.5%)未服用该药的患者中,疾病进展为新的血管形式。在第二部分的研究中,服用该药的患者全年平均接受了3.4±0.7次阿非利西普玻璃体内注射,而没有营养保健支持的对照组为5.3±1.2次。营养药物可有效降低中度黄斑变性演变为湿性黄斑变性的风险,因此建议湿性黄斑变性患者减少平均每年玻璃体内注射血管生成抑制剂的次数。
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来源期刊
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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