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Retina Today - 2013 Macula Society Musings (May/June 2013)

机译:今日视网膜-2013年Macula Society Musings(2013年5月/ 6月)

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Editora??s note: This blog was posted on April 24, 2013, to www.eyetube.net. Occasionally, we will be featuring content from our bloggers for retina in Retina Today. Nikolas London, MD, contributed the following, which details his experience at the 2013 Macula Society meeting. In late February of this year, I was lucky enough to ride the coattails of Paul Tornambe, MD, to the Macula Society meeting in Dana Point, CA. For my first blog entry for Retina Today, I provide a summary. Advanced Imaging Modalities For me, retinal imaging is beautiful and one of the most rewarding parts of the retina subspecialty. I am still excited by the array of modalities to evaluate the function and anatomy of the retina, and I particularly enjoy using these images to show my patients exactly what is happening to them and why, as well as how they are responding to treatment. Despite huge advances over the past decade, the envelope is still being pushed, and I pay particular attention to such talks at ophthalmology conferences. Richard Rosen, MD (New York Eye and Ear Institute), presented a novel technique called fluoro-microangiography, which is fluorescein angiography (FA) using an adaptive optics scanning laser ophthalmoscope (AO SLO). FA has been the gold standard for decades for evaluating the retinal vasculature and integrity of the blood-retinal barrier. AO SLO enables a much higher resolution assessment of the living retina at a cellular level. Dr. Rosen presented examples showing ultrastructural features of microaneurysms, beautiful images from normal subjects, as well as extended widefield imaging of the retinal periphery. Mark Pennesi, MD (Oregon Health and Science University), presented retinal imaging using flood-illuminated AO, which provided unprecedented resolution and detail of retinal structures, including the ability to calculate the density of cones in the perifoveal retina (ranges from 1300 to 1700 cones/degree2 in normal subjects). He illustrated how perifoveal cone density decreases slightly with age and drastically in diseases such as retinitis pigmentosa or Stargardt disease. These advances make the retina field particularly exciting for those of us dazzled by technology and hold the promise of improving our ability to care for our patients. Using less novel technology (but with no less interesting results), other talks focused on enhanced understanding of subtle symptoms of early age-related macular degeneration (AMD). Catherine Cukras, MD (National Eye Institute), presented data showing deficits in rod-mediated dark adaptation in non-advanced AMD. Moreover, Karl Csaky, MD (Texas Retina Associates), presented electroretinogram data demonstrating a progressive loss of rod sensitivity with advancing AMD. These studies provide some confirmation of patientsa?? subjective difficulties with dark adaptation. AMD Genetics The genetics of macular degeneration is a particularly hot field, holding promise to better define the risk for AMD progression and to illustrate potential therapeutic targets in the complicated cascade of events that contribute to advanced AMD. Numerous disease-associated single-nucleotide polymorphisms (SNPs) have been identified, including protective and detrimental markers. These include ARMS2, CHF, C2, C3, H3, and CFB. Nancy Holekamp, MD (Pepose Vision Institute), presented a comparison of 2 commercially available genetic tests for AMD, Sequenoma??s RetnaGene and Arctica??s Macula Risk. She found that they were discordant 60% of the time, with RetnaGene typically predicting the higher risk. On subsequent analysis, she noted that Macula Risk did not identify a moderate risk allele and appeared to misidentify it as a protective allele. It is important to note that this study was done on first-generation tests, while both companies have gone on to develop improved tests. In practice these tests can play a role in certain cir
机译:编者注:该博客于2013年4月24日发布到www.eyetube.net。有时,我们会在“今日的视网膜”中展示来自博客作者的内容。马里兰州的尼古拉斯·伦敦(Nikolas London)贡献了以下内容,详细介绍了他在2013年黄斑学会会议上的经历。在今年2月下旬,我很幸运地骑着MD的Paul Tornambe的长袍参加了在加州达纳角(Dana Point)举行的黄斑学会(Macula Society)会议。对于我今天在Retina上的第一个博客文章,我提供一个摘要。先进的成像方式对我而言,视网膜成像是美丽的,是视网膜亚专业最有价值的部分之一。我仍然对评估视网膜的功能和解剖结构的方式感到兴奋,并且我特别喜欢使用这些图像向我的患者确切显示他们的病情,原因以及他们对治疗的反应。尽管在过去的十年中取得了巨大的进步,但信封的使用仍在继续,我特别注意眼科会议上的此类演讲。医学博士理查德·罗森(Richard Rosen)(纽约眼耳研究所)介绍了一种称为荧光微血管造影的新技术,该技术是使用自适应光学扫描激光检眼镜(AO SLO)的荧光素血管造影(FA)。数十年来,FA一直是评估视网膜脉管系统和血视网膜屏障完整性的金标准。 AO SLO可以在细胞水平上对活的视网膜进行更高分辨率的评估。罗森博士介绍了一些示例,这些示例显示了微动脉瘤的超微结构特征,正常受试者的美丽图像以及视网膜周边的宽广域成像。俄勒冈健康与科学大学的医学博士Mark Pennesi介绍了使用泛光照明的AO进行视网膜成像的方法,它提供了前所未有的视网膜结构分辨率和细节,包括计算凹腔视网膜中视锥细胞密度的能力(范围为1300至1700)正常对象的视锥/度2)。他说明了在色素性视网膜炎或Stargardt病等疾病中,小凹周围锥体的密度如何随着年龄的增长而略有下降。这些进步使视网膜领域对于那些因技术而眼花azz乱的我们特别激动,并有望提高我们对患者的护理能力。其他演讲使用的是不太新颖的技术(但结果同样令人感兴趣),其重点是增强对与年龄有关的黄斑变性(AMD)的细微症状的理解。美国国家眼科学院的医学博士Catherine Cukras展示了数据,显示了非晚期AMD的杆介导的黑暗适应能力的缺陷。此外,医学博士(德克萨斯州视网膜协会)的Karl Csaky展示了视网膜电图数据,表明随着AMD的发展,视杆敏感性逐渐下降。这些研究为患者提供了一定的确认a?黑暗适应的主观困难。 AMD遗传学黄斑变性的遗传学是一个特别热门的领域,有望更好地确定AMD进展的风险,并阐明导致晚期AMD的一系列复杂事件中潜在的治疗靶标。已经鉴定出许多与疾病有关的单核苷酸多态性(SNP),包括保护性和有害性标志物。这些包括ARMS2,CHF,C2,C3,H3和CFB。医学博士南希·霍普坎普(Pepose Vision Institute)介绍了AMD的两种市售基因检测,Sequenoma的RetnaGene和Arctica的Macula Risk的比较。她发现他们有60%的时间不满意,而RetnaGene通常会预测更高的风险。在随后的分析中,她指出“黄斑风险”未能识别出中等风险等位基因,并且似乎将其误认为是保护性等位基因。重要的是要注意,这项研究是在第一代测试上完成的,而两家公司都在继续开发改进的测试。实际上,这些测试可以在某些情况下发挥作用

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