首页> 外文期刊>Retina >Genetic and environmental factors associated with reticular pseudodrusen in age-related macular degeneration
【24h】

Genetic and environmental factors associated with reticular pseudodrusen in age-related macular degeneration

机译:年龄相关性黄斑变性中网状假性鼻疽的遗传和环境因素

获取原文
获取原文并翻译 | 示例
           

摘要

PURPOSE: To analyze the genetic and environmental factors associated with reticular pseudodrusen (RPD) in age-related macular degeneration (AMD). METHODS: In a large population, AMD patients (n = 519) with and without RPD were assessed with a standardized examination including infrared images and spectral domain optical coherence tomography scans. Three groups were defined: Group 1: AMD patients with RPD (n = 105); Group 2: AMD patients without RPD (n = 414); and Group 3: controls with no AMD and no RPD (n = 430). Four genes associated with AMD (CFH, ARMS2/HTRA1, C3, apolipoprotein E) and environmental factors were assessed between the 3 groups. RESULTS: None of the environmental factors studied were more significantly associated to either Group 1 or Group 2. The odds ratios and 95% confidence intervals for individuals homozygous for the CFH risk allele were 4.0 (2.1-7.7) ([95% confidence interval: 2.1-7.7]; P < 0.0004) in Group 1 and 4.3 ([2.6-7.1]; P < 0.0004) in Group 2, compared with Group 3. The odds ratios for individuals homozygous for the ARMS2 risk allele for Groups 1 and 2 compared with Group 3 were 16.3 ([7.6-35.4]; P < 0.0004) and 11.9 ([6.3-22.3]; P < 0.0004), respectively. None of the genotypes studied were more significantly associated to Group 1 than Group 2. CONCLUSION: Genotypes known to be associated with AMD were similarly observed in patients with and without RPD.
机译:目的:分析与年龄相关性黄斑变性(AMD)的网状假性杜鲁森(RPD)相关的遗传和环境因素。方法:在大量人群中,有和没有RPD的AMD患者(n = 519)均接受了标准化检查,包括红外图像和光谱域光学相干断层扫描。分为三组:第1组:患有RPD的AMD患者(n = 105);第2组:无RPD的AMD患者(n = 414);第3组:无AMD和RPD的对照组(n = 430)。在这三组之间评估了与AMD相关的四个基因(CFH,ARMS2 / HTRA1,C3,载脂蛋白E)和环境因子。结果:研究的环境因素均与第1组或第2组没有更显着的相关性。CFH风险等位基因纯合子的比值比和95%置信区间为4.0(2.1-7.7)([95%置信区间:与组3相比,组1和组2分别为[2.1-7.7]; P <0.0004)(组2)[4.3- [2.6-7.1]; P <0.0004)。组1和2与ARMS2风险等位基因纯合的个体的优势比与第3组相比分别为16.3([7.6-35.4]; P <0.0004)和11.9([6.3-22.3]; P <0.0004)。研究的基因型与第1组的相关性没有一个比第2组更显着。结论:在患有和不患有RPD的患者中,观察到与AMD相关的基因型也相似。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号