Owsley Cynthia, Huisingh Carrie, Jackson Gregory R, Curcio Christine A, Szalai Alexander J, Dashti Nassrin, Clark Mark, Rookard Kia, McCrory Mark A, Wright Tyler T, Callahan Michael A, Kline Lanning B, Witherspoon C Douglas, McGwin Gerald
Department of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, United States.
Department of Ophthalmology, Penn State College of Medicine, Hershey, Pennsylvania, United States.
Invest Ophthalmol Vis Sci. 2014 May 22;55(8):4776-89. doi: 10.1167/iovs.14-14502.
Delayed rod-mediated dark adaptation (DA) is characteristic of early age-related macular degeneration (AMD) and also can be observed in some older adults in normal macular health. We examine cross-sectional associations between rod-mediated DA and risk factors for AMD in older adults in normal macular health.
The sample consisted of adults aged ≥60 years old in normal macular health per grading of fundus photos using an established disease classification system. Rod-mediated DA was measured psychophysically following a photobleach using a computer-automated dark adaptometer with targets centered at 5° on the inferior vertical meridian. The speed of DA was characterized by the rod-intercept value, with abnormal DA defined as rod-intercept ≥ 12.3 minutes. We assessed several health and functional characteristics that the literature has suggested increase AMD risk (e.g., smoking, alcohol use, inflammatory markers, apolipoproteins, low luminance visual acuity, chronic medical conditions, body mass, family history).
Among 381 participants (mean age, 68.5 years; SD, 5.5), 78% had normal and 22% had abnormal DA, with the prevalence of abnormal DA increasing with age. After age-adjustment, abnormal DA was associated with increased odds of elevated C-reactive protein (CRP), heavy use of or abstention from alcohol, high blood pressure, and drop in visual acuity under mesopic conditions.
Despite having normal macular health according to accepted definitions of AMD presence, approximately one-quarter of older adults recruited from primary eye care clinics had abnormal DA, which was associated with known risk factors for AMD, including elevated CRP.
延迟的视杆细胞介导的暗适应(DA)是早期年龄相关性黄斑变性(AMD)的特征,并且在黄斑健康正常的一些老年人中也可观察到。我们研究了黄斑健康正常的老年人中视杆细胞介导的DA与AMD危险因素之间的横断面关联。
样本包括年龄≥60岁、根据既定疾病分类系统对眼底照片进行分级显示黄斑健康正常的成年人。使用计算机自动暗适应计,在光漂白后以心理物理学方法测量视杆细胞介导的DA,目标位于下方垂直子午线5°处。DA的速度以视杆细胞截距值为特征,异常DA定义为视杆细胞截距≥12.3分钟。我们评估了文献中提示会增加AMD风险的几种健康和功能特征(例如,吸烟、饮酒、炎症标志物、载脂蛋白、低亮度视力、慢性疾病、体重、家族史)。
在381名参与者(平均年龄68.5岁;标准差5.5)中,78%的人DA正常,22%的人DA异常,异常DA的患病率随年龄增加。年龄调整后,异常DA与C反应蛋白(CRP)升高、大量饮酒或戒酒、高血压以及中度照明条件下视力下降的几率增加相关。
尽管根据公认的AMD存在定义黄斑健康正常,但从初级眼科诊所招募的老年人中约四分之一有异常DA,这与已知的AMD危险因素相关,包括CRP升高。