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首页> 外文期刊>Investigative ophthalmology & visual science >The Incidence and Progression of Reticular Drusen: Findings from an Older Australian Cohort
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The Incidence and Progression of Reticular Drusen: Findings from an Older Australian Cohort

机译:网状玻璃疣的发生和发展:澳大利亚老年人群的发现

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?Purpose?To assess 15-year incidence of reticular drusen (RDR) and their associations with known age-related macular degeneration (AMD) risk factors in an older Australian cohort. ?Methods?The Blue Mountains Eye Study examined 3654 participants aged 49+ years at baseline (1992-94), and re-examined 75.8, 76.5 and 56.1% of survivors 5, 10 and 15 years later, respectively. Retinal photographs were taken at each visit and DNA samples genotyped. Incidence and progression of RDR were confirmed using side-by-side grading from colour photographs. Incidence was estimated using the Kaplan-Meier product-limit survival method, controlling for competing risk of death. Associations between incidence of RDR and smoking, fish consumption, serum lipids, white cell count, and CFH-rs1061170 and ARMS2-rs10490924 single nucleotide polymorphisms were analyzed using discrete logistic regression models adjusting for age and sex. ?Results?The 15-year cumulative incidence of RDR was 4.0% (n=95); increasing from 0.4% in the age group 49-54 years to 7.0% in those aged 65-74 years, and then decreasing to 4.9% in those aged 75+ years (P for trend .0001). Women had a higher incidence of RDR compared to men (5.6% versus 2.2%, P=0.003). Increasing age (per decade; odds ratio, OR, 3.4; 95% confidence interval, CI, 2.6-4.4), female sex (OR 2.0, 95% CI 1.3-3.2) and presence of each risk allele of CFH (OR 1.8, 95% CI 1.3-2.4) or ARMS2 (OR 3.0, 95% CI 2.1-4.4) were associated with increased risk of developing RDR. Baseline current smokers had a significantly higher risk of RDR (OR 2.1, 95% CI 1.0-4.5) after adjusting for age, sex, and CFH and ARMS2 polymorphisms. Of 218 eyes with RDR (prevalent and incident cases), 40 eyes (18.4%) developed late AMD in 5 years (neovascular AMD 42.5%; geographic atrophy 57.5%). Total area of RDR or RDR extending to a near central location was found not to be associated with progression to late AMD in 5 years. A higher proportion of eyes with RDR located outside the macular area progressed to late AMD (36.4%), compared to those with RDR involving the macula area (10.1 and 22.2% for RDR within inner and outer subfields of the Wisconsin Grading grid, respectively). ?Conclusions?Known AMD risk factors were associated with increased long-term risk of developing RDR. RDR area and location were not associated with progression to late AMD over 5 years. ? Keywords: 504 drusen ? 412 age-related macular degeneration ? 463 clinical (human) or epidemiologic studies: prevalence/incidence ?.
机译:目的:评估澳大利亚人群中网状玻璃疣(RDR)的15年发病率及其与已知的年龄相关性黄斑变性(AMD)危险因素的关联。方法蓝山眼研究在基线(1992-94年)检查了3654名年龄在49岁以上的参与者,并分别在5、10和15年后重新检查了75.8%,76.5%和56.1%的幸存者。每次访问都拍摄视网膜照片,并对DNA样本进行基因分型。 RDR的发生率和进展通过彩色照片的并排分级来确认。使用Kaplan-Meier产品极限生存方法估算发病率,控制死亡的竞争风险。使用针对年龄和性别进行调整的离散逻辑回归模型,分析了RDR与吸烟,鱼类食用,血脂,白细胞计数以及CFH-rs1061170和ARMS2-rs10490924单核苷酸多态性的发生率之间的关联。结果:RDR的15年累积发生率为4.0%(n = 95);从49-54岁年龄段的0.4%上升到65-74岁年龄段的7.0%,然后下降到75岁以上年龄段的4.9%(趋势<.0001的P)。与男性相比,女性的RDR发生率更高(5.6%比2.2%,P = 0.003)。年龄增长(每十年;优势比,OR,3.4; 95%置信区间,CI,2.6-4.4),女性(OR 2.0,95%CI:1.3-3.2)和CFH的每个风险等位基因存在(OR,1.8, 95%CI 1.3-2.4)或ARMS2(OR 3.0,95%CI 2.1-4.4)与发展RDR的风险增加相关。在调整了年龄,性别,CFH和ARMS2多态性后,当前的基线吸烟者具有较高的RDR风险(OR 2.1,95%CI 1.0-4.5)。在218例患有RDR的眼中(普遍和偶发病例),有40眼(占18.4%)在5年内出现晚期AMD(血管性AMD为42.5%;地理性萎缩为57.5%)。发现RDR的总面积或延伸至近中心位置的RDR与5年内晚期AMD的进展无关。与具有黄斑区域的RDR相比,位于黄斑区域之外的RDR的眼睛进展到晚期AMD(36.4%)(在威斯康星州分级网格的内部和外部子区域中的RDR分别为10.1和22.2%) 。结论:已知的AMD危险因素与发展RDR的长期风险增加有关。 RDR的面积和位置与5年内晚期AMD的进展无关。 ?关键字:504玻璃疣? 412年龄相关性黄斑变性? 463临床(人类)或流行病学研究:患病率/发病率?

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