NORC, University of Chicago, Chicago, Illinois.
Institute for Health Metrics and Evaluation, University of Washington, Seattle.
JAMA Ophthalmol. 2022 Dec 1;140(12):1202-1208. doi: 10.1001/jamaophthalmol.2022.4401.
Age-related macular degeneration (AMD) is a leading cause of vision loss and blindness. AMD prevalence has not been estimated for the US in over a decade and early-stage AMD prevalence estimates are scarce and inconsistently measured.
To produce estimates of early- and late-stage AMD prevalence overall and by age, gender, race and ethnicity, county, and state.
DESIGN, SETTING, AND PARTICIPANTS: The study team conducted a bayesian meta-regression analysis of relevant data sources containing information on the prevalence of AMD among different population groups in the US.
We included data from the American Community Survey (2019), the National Health and Nutrition Examination Survey (2005-2008), US Centers for Medicare & Medicaid Services claims for fee-for-service beneficiaries (2018), and population-based studies (2004-2016).
We included all relevant data from the US Centers for Disease Control and Prevention's Vision and Eye Health Surveillance System.
The prevalence of early- and late-stage AMD was estimated and stratified when possible by factors including county, age group, gender, and race and ethnicity. Data analysis occurred from June 2021 to April 2022.
The prevalence of early- (defined as retinal pigment epithelium abnormalities or the presence of drusen 125 or more microns in diameter in either eye) and late-stage (defined as choroidal neovascularization and/or geographic atrophy in either eye) manifestations of AMD.
This study used data from nationally representative and local population-based studies that represent the populations in which they were conducted. For 2019, we estimated that there were 18.34 million people 40 years and older (95% uncertainty interval [UI], 15.30-22.03) living with early-stage AMD, corresponding to a crude prevalence rate of 11.64% (95% UI, 9.71-13.98). We estimated there were 1.49 million people 40 years and older (95% UI, 0.97-2.15) living with late-stage AMD, corresponding to a crude prevalence rate of 0.94% (95% UI, 0.62-1.36). Prevalence rates of early- and late-stage AMD varied by demographic characteristics and geography.
We estimated a higher prevalence of early-stage AMD and a similar prevalence of late-stage AMD as compared with earlier studies. State-level and county-level AMD estimates may help guide public health practice.
年龄相关性黄斑变性(AMD)是导致视力丧失和失明的主要原因。美国已经有十多年没有估计过 AMD 的患病率,而且早期 AMD 的患病率估计数据稀缺且测量方法不一致。
总体以及按年龄、性别、种族和民族、县和州来估计早期和晚期 AMD 的患病率。
设计、设置和参与者:研究团队对包含美国不同人群 AMD 患病率信息的相关数据源进行了贝叶斯元回归分析。
我们纳入了来自美国社区调查(2019 年)、国家健康和营养调查(2005-2008 年)、美国医疗保险和医疗补助服务中心(CMS)按服务收费受益人的索赔数据(2018 年)以及基于人群的研究(2004-2016 年)的数据。
我们纳入了美国疾病控制与预防中心(CDC)视觉和眼健康监测系统的所有相关数据。
按县、年龄组、性别以及种族和民族等因素对早期和晚期 AMD 的患病率进行了估计和分层。数据分析于 2021 年 6 月至 2022 年 4 月进行。
早期(定义为视网膜色素上皮异常或双眼直径 125 微米或更大的沉积物存在)和晚期(定义为双眼脉络膜新生血管和/或地图样萎缩)AMD 表现的患病率。
本研究使用了来自全国代表性和基于人群的本地研究的数据,这些研究代表了其所在人群。对于 2019 年,我们估计有 1834 万 40 岁及以上人群(95%不确定区间[UI],15.30-22.03)患有早期 AMD,粗患病率为 11.64%(95% UI,9.71-13.98)。我们估计有 149 万 40 岁及以上人群(95% UI,0.97-2.15)患有晚期 AMD,粗患病率为 0.94%(95% UI,0.62-1.36)。早期和晚期 AMD 的患病率因人口统计学特征和地理位置而异。
与早期研究相比,我们估计早期 AMD 的患病率更高,晚期 AMD 的患病率相似。州和县级 AMD 估计值可能有助于指导公共卫生实践。