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临床前期年龄相关性黄斑变性的视网膜结构

Retinal Structure in Pre-Clinical Age-Related Macular Degeneration.

作者信息

Nusinowitz S, Wang Y, Kim P, Habib S, Baron R, Conley Y, Gorin M

机构信息

a Department of Ophthalmology , David Geffen School of Medicine-UCLA, Stein Eye Institute , Los Angeles , CA , USA.

b Department of Human Genetics, Graduate School of Public Health , University of Pittsburgh , Pittsburgh , PA , USA.

出版信息

Curr Eye Res. 2018 Mar;43(3):376-382. doi: 10.1080/02713683.2017.1401646. Epub 2017 Nov 14.

Abstract

PURPOSE

To determine, if there are identifiable retinal structural changes associated with genetic risk for age-related macular degeneration (AMD).

MATERIALS AND METHODS

Seventy-three subjects (range 51.5 to 68.9 years) participated in this prospective study. Subjects were recruited based on the presence of a family history of AMD in one or both parents. All participants underwent a complete ophthalmic exam and imagery for staging of disease severity and genetic testing to assess genetic risk for AMD development. Optical coherence tomography (OCT) imaging was performed on all participants. Semi-automated retinal layer segmentation was performed to assess retinal structural changes.

RESULTS

Of 73 subjects, 47 subjects had normal appearing retina with no evidence of drusen or other changes consistent with AMD, 16 subjects were classified as early AMD, and 13 were designated as intermediate AMD. Retinal volume measures of total retina, outer retina, outer nuclear layer and the retinal pigment epithelium, were not related to AMD classification, genetic risk scores, or age. The thickness of the outer retina showed statistically significant thickening in the foveal region in only the intermediate AMD group and a statistically significant thickening of the RPE in early and intermediate AMD groups in the central retina.

CONCLUSION

No consistent changes were observed in retinal structure at multiple locations that are associated with pre-clinical AMD, based on AMD genetic risk or with aging within the age range of our cohort.

摘要

目的

确定是否存在与年龄相关性黄斑变性(AMD)遗传风险相关的可识别视网膜结构变化。

材料与方法

73名受试者(年龄范围51.5至68.9岁)参与了这项前瞻性研究。根据父母一方或双方存在AMD家族史招募受试者。所有参与者均接受了全面的眼科检查和影像学检查,以对疾病严重程度进行分期,并进行基因检测以评估AMD发生的遗传风险。对所有参与者进行了光学相干断层扫描(OCT)成像。进行半自动视网膜层分割以评估视网膜结构变化。

结果

73名受试者中,47名受试者视网膜外观正常,无玻璃膜疣或其他与AMD一致的变化迹象,16名受试者被分类为早期AMD,13名被指定为中期AMD。视网膜总体积、外层视网膜、外核层和视网膜色素上皮的测量值与AMD分类、遗传风险评分或年龄无关。仅在中期AMD组中,外层视网膜厚度在黄斑区显示出统计学上的显著增厚,而在早期和中期AMD组中,视网膜中央区域的视网膜色素上皮有统计学上的显著增厚。

结论

基于AMD遗传风险或我们队列年龄范围内的衰老情况,在与临床前期AMD相关的多个位置未观察到视网膜结构的一致变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/138a/6217942/865b0a369269/nihms-1502386-f0001.jpg

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