Huisingh Carrie, McGwin Gerald, Neely David, Zarubina Anna, Clark Mark, Zhang Yuhua, Curcio Christine A, Owsley Cynthia
Department of Ophthalmology University of Alabama at Birmingham, Birmingham, Alabama, United States.
Department of Ophthalmology University of Alabama at Birmingham, Birmingham, Alabama, United States 2Department of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama, United States.
Invest Ophthalmol Vis Sci. 2016 Feb;57(2):739-45. doi: 10.1167/iovs.15-18316.
Subretinal drusenoid deposits (SDD) have been associated with the progression to late age-related macular degeneration (AMD). To determine whether SDD in eyes in normal macular health increases risk for early AMD, this study examined the association between presence of SDD at baseline in a cohort of older adults in normal macular health and incident AMD 3 years later.
Subjects enrolled in the Alabama Study on Early Age-Related Macular Degeneration (ALSTAR) were assessed for the presence of SDD using color fundus photos, infrared reflectance and fundus autofluorescence images, and spectral-domain optical coherence tomography volumes. The study sample included 799 eyes from 455 participants in normal macular health per grading of color fundus photographs using the 9-step Age-Related Eye Disease Study (AREDS) classification system. Age-related macular degeneration was defined as eyes having an AREDS grade ≥2 at the 3-year follow-up.
Twenty-five percent of participants had SDD in one or both eyes at baseline. At follow-up visit, 11.9% of eyes in the sample developed AMD. Compared to eyes without SDD, those with SDD were 2.24 (95% confidence interval [CI] 1.36-3.70) times more likely to have AMD at follow-up. After adjusting for age, C-reactive protein quartile, and family history of AMD, the association persisted.
Results suggest that SDD in older eyes with normal macular health as defined by the AREDS scale is a risk factor for the development of early AMD. Older adults in seemingly normal macular health yet having SDD may warrant closer clinical monitoring for the possible onset of early AMD.
视网膜下玻璃膜疣样沉积物(SDD)与晚期年龄相关性黄斑变性(AMD)的进展相关。为了确定黄斑健康正常的眼中的SDD是否会增加早期AMD的风险,本研究调查了一组黄斑健康正常的老年人基线时SDD的存在与3年后发生AMD之间的关联。
对参加阿拉巴马州早期年龄相关性黄斑变性研究(ALSTAR)的受试者,使用彩色眼底照片、红外反射和眼底自发荧光图像以及光谱域光学相干断层扫描容积评估SDD的存在情况。研究样本包括455名参与者的799只眼,这些参与者的黄斑健康正常,使用9步年龄相关性眼病研究(AREDS)分类系统对彩色眼底照片进行分级。年龄相关性黄斑变性定义为在3年随访时AREDS分级≥2级的眼。
25%的参与者在基线时一只或两只眼睛有SDD。在随访时,样本中11.9%的眼睛发生了AMD。与没有SDD的眼睛相比,有SDD的眼睛在随访时发生AMD的可能性高2.24倍(95%置信区间[CI]1.36 - 3.70)。在调整年龄、C反应蛋白四分位数和AMD家族史后,这种关联仍然存在。
结果表明,根据AREDS量表定义的黄斑健康正常的老年眼中的SDD是早期AMD发生的一个危险因素。黄斑健康看似正常但有SDD的老年人可能需要更密切的临床监测以观察早期AMD的可能发病情况。