Université de Bordeaux, INSERM, Bordeaux Population Health Research Center, Team Lifelong Exposures, Health, and Aging (LEHA), UMR 1219, Bordeaux, France.
Service d'Ophtalmologie, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
JAMA Ophthalmol. 2018 May 1;136(5):473-481. doi: 10.1001/jamaophthalmol.2018.0504.
While the prevalence of age-related macular degeneration (AMD) differs according to continents and races/ethnicities, its incidence in the European continent has been scarcely documented.
To describe the incidence and associated risk factors of AMD in elderly French individuals.
DESIGN, SETTING, AND PARTICIPANTS: This population-based cohort study of 963 residents of Bordeaux, France, who were 73 years or older at baseline and participated in the Antioxydants, Lipides Essentiels, Nutrition et Maladies Oculaires (ALIENOR) Study between October 2, 2006, and December 21, 2012. Of 829 participants at risk for incident AMD, 659 (79.5%) were observed for a mean (SD) duration of 3.8 (1.1) years. Data were analyzed from August 2016 to March 2017.
Age-related macular degeneration was graded from retinal photographs and spectral-domain optical coherence tomography into 5 exclusive stages: no AMD, early AMD1, early AMD2, late atrophic AMD, and late neovascular AMD.
Of the 659 eligible participants, 413 (62.7%) were women, and the mean (SD; range) age was 79.7 (4.4; 73-94) years. A total of 120 incident cases of early AMD and 45 incident cases of advanced AMD were recorded. Incidence rates of early and advanced AMD were 79.9 (95% CI, 66.8-95.5) per 1000 person-years and 18.6 (95% CI, 13.9-24.9) per 1000 person-years, respectively, corresponding to 5-year risks of 32.9% and 8.9%. Incidence of advanced AMD per 1000 eye-years was 1.5 in eyes without any AMD at baseline, 42.4 in those with early AMD1, and 85.1 in those with early AMD2. In multivariate analysis without correction for multiple testing, progression from early to advanced AMD was associated with AMD grade in the fellow eye (hazard ratio [HR] according to grade, 13.0 [95% CI, 2.8-61.2] to 22.5 [95% CI, 2.6-195.9]), having smoked at least 20 pack-years (calculated as number of smoking years × mean number of cigarettes per day / 20; HR, 3.0; 95% CI, 1.4-6.5), and complement factor H (CFH) Y402H genotype (CC genotype: HR, 2.3; 95% CI, 1.0-5.3; TC genotype: HR, 1.5; 95% CI, 0.6-3.7). Incidence of early AMD was associated with early AMD in the fellow eye (early AMD1: HR, 2.6; 95% CI, 1.6-4.2; early AMD2: HR, 5.6; 95% CI, 3.3-9.4) and high plasma high-density lipoprotein cholesterol levels (HR, 1.2; 95% CI, 1.0-1.4).
In this cohort, AMD incidence rates were similar to those observed in other European populations. This study suggests a high risk for incident early AMD in individuals with high plasma high-density lipoprotein cholesterol levels while confirming the high risk for progression from early to advanced AMD in heavy smokers and carriers of CFH Y402H at-risk genotypes.
重要性:虽然年龄相关性黄斑变性(AMD)的流行程度因大陆和种族/民族而异,但欧洲大陆 AMD 的发病率鲜有记录。
目的:描述法国老年人群 AMD 的发病率及其相关危险因素。
设计、地点和参与者:这是一项基于人群的队列研究,纳入了法国波尔多的 963 名 73 岁及以上的居民,他们参加了 Antioxydants,Lipides Essentiels,Nutrition et Maladies Oculaires(ALIENOR)研究,研究时间为 2006 年 10 月 2 日至 2012 年 12 月 21 日。在有患 AMD 风险的 829 名参与者中,有 659 名(79.5%)参与者的平均(SD)随访时间为 3.8(1.1)年。数据分析于 2016 年 8 月至 2017 年 3 月进行。
主要结局和测量:AMD 通过视网膜照片和光谱域光学相干断层扫描分为 5 个独立阶段:无 AMD、早期 AMD1、早期 AMD2、晚期萎缩性 AMD 和晚期新生血管性 AMD。
结果:在 659 名符合条件的参与者中,413 名(62.7%)为女性,平均(SD;范围)年龄为 79.7(4.4;73-94)岁。共记录到 120 例早期 AMD 病例和 45 例晚期 AMD 病例。早期和晚期 AMD 的发病率分别为 79.9(95%CI,66.8-95.5)/1000 人年和 18.6(95%CI,13.9-24.9)/1000 人年,相应的 5 年风险分别为 32.9%和 8.9%。在基线时没有任何 AMD 的眼睛中,每 1000 眼年的晚期 AMD 发病率为 1.5,早期 AMD1 的发病率为 42.4,早期 AMD2 的发病率为 85.1。在未经多重检验校正的多变量分析中,从早期到晚期 AMD 的进展与对侧眼的 AMD 分级相关(按分级计算的风险比[HR],13.0[95%CI,2.8-61.2]至 22.5[95%CI,2.6-195.9])、至少吸烟 20 包年(计算方法为吸烟年数×每天平均吸烟支数/20;HR,3.0;95%CI,1.4-6.5)和补体因子 H(CFH)Y402H 基因型(CC 基因型:HR,2.3;95%CI,1.0-5.3;TC 基因型:HR,1.5;95%CI,0.6-3.7)。早期 AMD 的发病率与对侧眼的早期 AMD 相关(早期 AMD1:HR,2.6;95%CI,1.6-4.2;早期 AMD2:HR,5.6;95%CI,3.3-9.4)和高血浆高密度脂蛋白胆固醇水平(HR,1.2;95%CI,1.0-1.4)。
结论和相关性:在本队列中,AMD 的发病率与其他欧洲人群观察到的发病率相似。这项研究表明,高血浆高密度脂蛋白胆固醇水平的个体发生早期 AMD 的风险较高,而重度吸烟者和携带 CFH Y402H 风险基因型的个体从早期到晚期 AMD 的进展风险较高。