Keilhauer Claudia N, Fritsche Lars G, Weber Bernhard H F
Department of Ophthalmology, University of Wuerzburg, Germany.
Ophthalmic Genet. 2011 Nov;32(4):237-44. doi: 10.3109/13816810.2011.592177. Epub 2011 Jul 8.
Age-related macular degeneration (AMD) is a complex disease caused by genetic and environmental factors. Monozygotic twins with late stage AMD provide an opportunity to evaluate the role of environmental factors on a genetically uniform background.
Monozygosity was determined in four twin pairs by genotyping 15 highly polymorphic tetranucleotide repeat markers. Clinically, the monozygotic twin pairs were evaluated by ophthalmologic examination, fundus autofluorescence (FAF) imaging, and, upon suspicion of choroidal neovascular membranes, by fluorescein angiography. Twin pairs were followed over a period of 4-8 years.
Genetically confirmed monozygotic twins with early stages of AMD reveal striking symmetry of early macular pathology. Upon progression to late stage AMD each twin pair developed a discordant phenotype with respect to disease onset and specific phenotype as choroidal neovascularization (CNV) and geographic atrophy (GA).
Genetic risk variants are known to predispose to the development of AMD. Course and visual outcome of the disease, however, appear to be influenced by environmental factors rather than genetic determinants.
年龄相关性黄斑变性(AMD)是一种由遗传和环境因素引起的复杂疾病。患有晚期AMD的同卵双胞胎提供了一个在基因背景一致的情况下评估环境因素作用的机会。
通过对15个高度多态性的四核苷酸重复标记进行基因分型,确定了四对双胞胎的同卵性。临床上,通过眼科检查、眼底自发荧光(FAF)成像,以及在怀疑有脉络膜新生血管膜时进行荧光素血管造影,对同卵双胞胎进行评估。对双胞胎进行了4至8年的随访。
经基因确认的患有早期AMD的同卵双胞胎显示出早期黄斑病变的显著对称性。在进展到晚期AMD时,每对双胞胎在疾病发作和特定表型(如脉络膜新生血管形成(CNV)和地图样萎缩(GA))方面出现了不一致的表型。
已知遗传风险变异易导致AMD的发生。然而,该疾病的病程和视觉结果似乎受环境因素而非遗传决定因素的影响。