Bressler Neil M, Bressler Susan B, Congdon Nathan G, Ferris Frederick L, Friedman David S, Klein Ronald, Lindblad Anne S, Milton Roy C, Seddon Johanna M
Arch Ophthalmol. 2003 Nov;121(11):1621-4. doi: 10.1001/archopht.121.11.1621.
To estimate the potential public health impact of the findings of the Age-Related Eye Disease Study (AREDS) on reducing the number of persons developing advanced age-related macular degeneration (AMD) during the next 5 years in the United States.
The AREDS clinical trial provides estimates of AMD progression rates and of reduction in risk of developing advanced AMD when a high-dose nutritional supplement of antioxidants and zinc is used. These results are applied to estimates of the US population at risk, to estimate the number of people who would potentially avoid advanced AMD during 5 years if those at risk were to take a supplement such as that used in AREDS.
An estimated 8 million persons at least 55 years old in the United States have monocular or binocular intermediate AMD or monocular advanced AMD. They are considered to be at high risk for advanced AMD and are those for whom the AREDS formulation should be considered. Of these people, 1.3 million would develop advanced AMD if no treatment were given to reduce their risk. If all of these people at risk received supplements such as those used in AREDS, more than 300,000 (95% confidence interval, 158,000-487,000) of them would avoid advanced AMD and any associated vision loss during the next 5 years.
If people at high risk for advanced AMD received supplements such as those suggested by AREDS results, the potential impact on public health in the United States would be considerable during the next 5 years.
评估年龄相关性眼病研究(AREDS)的研究结果对未来5年美国延缓晚期年龄相关性黄斑变性(AMD)患者数量增长的潜在公共卫生影响。
AREDS临床试验提供了AMD进展率的估计值,以及使用高剂量抗氧化剂和锌营养补充剂时晚期AMD发病风险降低情况的估计值。将这些结果应用于美国高危人群的估计数据,以估算如果高危人群服用AREDS中使用的此类补充剂,在5年内可能避免发展为晚期AMD的人数。
在美国,估计有800万至少55岁的人患有单眼或双眼中度AMD或单眼晚期AMD。他们被认为是晚期AMD的高危人群,也是应考虑使用AREDS配方的人群。如果不采取降低风险的治疗措施,这些人中有130万将发展为晚期AMD。如果所有这些高危人群都服用AREDS中使用的此类补充剂,那么在未来5年内,其中超过30万(95%置信区间为15.8万至48.7万)的人将避免发展为晚期AMD以及任何相关的视力丧失。
如果晚期AMD高危人群服用AREDS结果所建议的此类补充剂,在未来5年对美国公共卫生的潜在影响将是巨大的。