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The age-related eye disease study 2 (AREDS2): Study design and baseline characteristics (AREDS2 Report Number 1)

机译:年龄相关性眼病研究2(AREDS2):研究设计和基线特征(AREDS2报告编号1)

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Purpose: The Age-Related Eye Disease Study (AREDS) demonstrated beneficial effects of oral supplementation with antioxidant vitamins and minerals on the development of advanced age-related macular degeneration (AMD) in persons with at least intermediate AMD (bilateral large drusen with or without pigment changes). Observational data suggest that other oral nutrient supplements might further reduce the risk of progression to advanced AMD. The primary purpose of the Age-Related Eye Disease Study 2 (AREDS2) is to evaluate the efficacy and safety of lutein plus zeaxanthin (L+Z) and/or ω-3 long-chain polyunsaturated fatty acid (LCPUFA) supplementation in reducing the risk of developing advanced AMD. The study also assesses the reduction in zinc and the omission of β-carotene from original AREDS formulation. Design: Multicenter, phase III, randomized, controlled clinical trial. Participants: Persons aged 50 to 85 with bilateral intermediate AMD or advanced AMD in 1 eye. Methods: All participants were randomly assigned to placebo (n = 1012), L+Z (10 mg/2 mg; n = 1044), ω-3 LCPUFAs (eicosapentaenoic acid + docosahexaenoic acid [650 mg/350 mg]; n = 1069), or the combination of L+Z and ω-3 LCPUFAs (n = 1078). All participants were offered a secondary randomization to 1 of 4 variations of the original AREDS formulation keeping vitamins C (500 mg) and E (400 IU) and copper (2 mg) unchanged while varying zinc and β-carotene as follows: Zinc remains at the original level (80 mg), lower only zinc to 25 mg, omit β-carotene only, or lower zinc to 25 mg and omit β-carotene. Main Outcome Measures: Progression to advanced AMD determined by centralized grading of annual fundus photographs. Results: We enrolled 4203 participants at 82 clinical centers located in the United States. Population characteristics at baseline were as follows: Mean age, 74 years; 57% female; 97% white; 7% current smokers; 19% with prior cardiovascular disease; and 44% and 50% taking statin-class cholesterol-lowering drugs and aspirin, respectively. Ocular characteristics include 59% with bilateral large drusen, 32% with advanced AMD in 1 eye and mean visual acuity of 20/32 in eyes without advanced AMD. Conclusions: This report presents the AREDS2 study design and the participants' baseline demographic and ocular characteristics. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.
机译:目的:年龄相关性眼病研究(AREDS)证明,口服抗氧化剂维生素和矿物质补充剂对至少具有中度AMD(双侧大玻璃疣或有或无双眼)的人发展与年龄相关的高级黄斑变性(AMD)具有有益作用颜料变化)。观察数据表明,其他口服营养补充剂可能会进一步降低进展为晚期AMD的风险。与年龄有关的眼疾研究2(AREDS2)的主要目的是评估叶黄素加玉米黄质(L + Z)和/或ω-3长链多不饱和脂肪酸(LCPUFA)补充剂在减少视网膜色素变性方面的功效和安全性。罹患晚期AMD的风险。该研究还评估了原始AREDS配方中锌的减少和β-胡萝卜素的遗漏。设计:多中心III期随机对照临床试验。参加者:50至85岁的双眼中度AMD或晚期AMD的人为一只眼。方法:将所有参与者随机分配至安慰剂(n = 1012),L + Z(10 mg / 2 mg; n = 1044),ω-3LCPUFAs(二十碳五烯酸+二十二碳六烯酸[650 mg / 350 mg]; n = 1069),或L + Z和ω-3LCPUFA的组合(n = 1078)。所有参与者均获得了原始AREDS配方的4种变化中的1种的二次随机化,其中维生素C(500 mg)和E(400 IU)和铜(2 mg)保持不变,而锌和β-胡萝卜素的变化如下:锌保持在原始水平(80毫克),仅将锌降低至25毫克,仅省略β-胡萝卜素,或将锌降低至25毫克并省略β-胡萝卜素。主要结果指标:通过对年度眼底照片进行集中分级确定向高级AMD的进展。结果:我们在美国的82个临床中心招募了4203名参与者。基线时的人口特征如下:平均年龄74岁;平均年龄74岁。女性占57%;白色97%;目前吸烟者的7%; 19%患有先前的心血管疾病;服用他汀类降胆固醇药物和阿司匹林的比例分别为44%和50%。眼部特征包括59%的双侧大玻璃膜疣,32%的1只眼患有晚期AMD,而无晚期AMD的眼平均视力为20/32。结论:本报告介绍了AREDS2研究设计以及参与者的基线人口统计学和眼科特征。财务披露:在参考文献之后可以找到专有或商业披露。

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