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Baseline characteristics and age-related macular degeneration in participants of the “ASPirin in Reducing Events in the Elderly” (ASPREE)-AMD trial

机译:“阿司匹林减少老年人事件中的阿司匹林”(Aspreee)-Amd试验中的基线特征和年龄相关性黄斑变性

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PurposeTo describe the baseline participant characteristics in the ASPREE-AMD study, investigating the effect of aspirin on AMD incidence and progression.MethodsAustralian participants from the ASPirin in Reducing Events in the Elderly (ASPREE) trial, randomized to 100?mg aspirin daily or placebo, had non-mydriatic, digital color fundus images graded according to the Beckman AMD classification. Associations with AMD were determined for baseline characteristics and genetic risk variants.ResultsASPREE-AMD sub-study enrolled 4993 participants with gradable macular images. Median age was 73.4 years (IQR, 71.5, 76.6), 52% were female, 10% had diabetes mellitus, 73% had hypertension, and 44% were former/current smokers. Early, intermediate and late AMD (detected in 20.6%, 16.1%, 1.1%, respectively), significantly associated with age, were also associated with increasing HDL levels: OR?=?1.52 (95%CI, 1.26, 1.84), OR?=?1.43 (1.17, 1.77) and OR?=?1.96 (1.02, 3.76), respectively. Female sex was associated with early [OR?=?1.37 (1.16, 1.62)], and intermediate [OR?=?1.35 (1.12, 1.63)] AMD, as was previous regular use of aspirin, with OR?=?1.46 (1.11, 1.92) and OR?=?1.37 (1.01, 1.85), respectively. Current smoking had increased odds for late AMD, OR?=?4.02 (1.42, 11.36). Genetic risk variant rs3750846 (ARMS2/HTRA1) was associated with each AMD stage (p?
机译:Purposeto描述了Asprie-AMD研究中的基线参与者特征,调查阿司匹林对AMD发病率和进展的影响。从阿司匹林中的Aspirin参与者在减少老年人(Aspree)试验中的事件中,随机化为100?Mg Aspirin日常或安慰剂,有非瞳孔,数字彩色眼底图像根据Beckman AMD分类进行分级。确定与AMD的关联是基线特征和遗传风险变体。评估4993名与渐进式黄斑图像的参与者注册了4993个参与者。中位年龄为73.4岁(IQR,71.5,76.6),52%是女性,10%的糖尿病患有糖尿病,73%的高血压,44%是前/目前的吸烟者。早期,中期和晚期AMD(检测到20.6%,16.1%,1.1%)与年龄显着相关,同样与增加的HDL水平有关:或?=?1.52(95%CI,1.26,1.84),或?=?1.43(1.17,1.77)和或?=?1.96(1.02,3.76)。女性与早期[或?=?1.37(1.16,1.62)]和中间[或?=?1.35(1.12,112,1.63)] AMD,正常使用阿司匹林,有或?=?1.46( 1.11,1.92)和或?=?1.37(1.01,1.85)。目前的吸烟可能会增加amd或?=?4.02(1.42,11.36)。遗传风险变量RS3750846(ARMS2 / HTRA1)与每个AMD阶段(P?<0.001),风险变体RS570618和RS10922109(CFH)有关,具有中间和晚期(P?<0.001),罕见变种RS147859257(C3 )有晚期(p?<0.001)。随机组对所有分析的AMD危险因素进行了良好的平衡。结合的协会是AMD的典型。 Aspree-AMD临床试验提供了独特的机会,以确定低剂量阿司匹林在老年人群体中的低剂量阿司匹林的风险和益处.Trial登录申请新西兰临床试验登记处:ACTRN 12613000755730。

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