Costa Inês, Carvalho Ana, Andrade Helton, Pereira Bruno, Camacho Pedro
H&TRC-Health & Technology Research Center, ESTeSL Escola Superior de Tecnologia da Saúde, Instituto Politécnico de Lisboa, Lisbon 1990-096, Portugal.
Escola Superior de Tecnologia da Saúde de Lisboa, Instituto Politécnico de Lisboa, Lisboa 1990-096, Portugal.
Int J Ophthalmol. 2025 Jan 18;18(1):103-110. doi: 10.18240/ijo.2025.01.12. eCollection 2025.
To quantify and compare longitudinal thickness changes of the ganglion cell complex (GCC) and the choroid in patients with different patterns of age-related macular degeneration (AMD) progression.
Retrospective cohort analysis of anonymized data from participants aged 50y or more and diagnosed with early/intermediate AMD in at least one eye (with no evidence of advanced AMD). A total of 64 participants were included from the Instituto de Retina de Lisboa (IRL) study (IPL/2022/MetAllAMD_ESTeSL) and divided into 4 groups according to the Rotterdam classification for AMD. Spectral domain optical coherence tomography (SD-OCT) was used to assess and quantify GCC and choroid thickness at two time points (first visit last visit) with a minimum interval of 3y.
In the GCC inner ring, a thinner thickness (=0.001) was observed in the atrophic AMD group (51.3±21.4 µm) compared to the early AMD (84.3±11.5 µm), intermediate AMD (77.6±16.1 µm) and neovascular AMD (88.9±16.3 µm) groups. Choroidal thickness quantification showed a generalized reduction in the central circle (=0.002) and inner ring (=0.001). Slight reductions in retinal thickness were more accentuated in the inner ring in the atrophic AMD (-13%; <0.01).
The variation of the analyzed structures could be an indicator of risk of progression with neurodegenerative (GCC) or vascular (choroid) pattern in the intermediate and atrophic AMD. The quantification of both structures can provide important information about the risk of disease progression in the early and intermediate stages but also for the evolution pattern into late stages (atrophic or neovascular).
量化并比较不同年龄相关性黄斑变性(AMD)进展模式患者神经节细胞复合体(GCC)和脉络膜的纵向厚度变化。
对年龄在50岁及以上、至少一只眼睛被诊断为早期/中期AMD(无晚期AMD证据)的参与者的匿名数据进行回顾性队列分析。从里斯本视网膜研究所(IRL)研究(IPL/2022/MetAllAMD_ESTeSL)中纳入了64名参与者,并根据AMD的鹿特丹分类将其分为4组。使用光谱域光学相干断层扫描(SD-OCT)在两个时间点(首次就诊和末次就诊)评估并量化GCC和脉络膜厚度,最小间隔为3年。
在GCC内环,与早期AMD组(84.3±11.5 µm)、中期AMD组(77.6±16.1 µm)和新生血管性AMD组(88.9±16.3 µm)相比,萎缩性AMD组(51.3±21.4 µm)的厚度更薄(P=0.001)。脉络膜厚度量化显示中央环(P=0.002)和内环(P=0.001)普遍变薄。视网膜厚度的轻微减少在萎缩性AMD的内环更为明显(-13%;P<0.01)。
所分析结构的变化可能是中期和萎缩性AMD中神经退行性(GCC)或血管性(脉络膜)模式进展风险的指标。对这两种结构的量化可以提供有关疾病在早期和中期进展风险的重要信息,也可为晚期(萎缩性或新生血管性)的演变模式提供信息。