El-Mulki Omar S, Berni Alessandro, Kastner James, Shen Mengxi, Cheng Yuxuan, Herrera Gissel, Beqiri Sara, Trivizki Omer, Le Viet-Hoan, Sivathanu Kumar Bhagavath, Di Nicola Maura, O'Brien Robert, Waheed Nadia K, Gregori Giovanni, Wang Ruikang K, Rosenfeld Philip J
Department of Ophthalmology, Bascom Palmer Eye Institute (O.S.E.M., A.B., J.K., M.S., G.H., S.B., O.T., M.D.N., R.O.B., G.G., P.J.R.), University of Miami Miller School of Medicine, Miami, Florida, USA.
Department of Ophthalmology, Bascom Palmer Eye Institute (O.S.E.M., A.B., J.K., M.S., G.H., S.B., O.T., M.D.N., R.O.B., G.G., P.J.R.), University of Miami Miller School of Medicine, Miami, Florida, USA; Department of Ophthalmology (A.B.), IRCCS San Raffaele Scientific Institute, Milan, Italy.
Am J Ophthalmol. 2025 Oct;278:402-412. doi: 10.1016/j.ajo.2025.07.001. Epub 2025 Jul 6.
This study used en face swept-source optical coherence tomography (SS-OCT) imaging to follow eyes with intermediate age-related macular degeneration (iAMD) in the presence and absence of calcified drusen (CaD) to determine if the presence and size of CaD increased the risk of forming large choroidal hypertransmission defects (hyperTDs).
Post hoc subgroup analysis of a prospective cohort study.
Eyes with iAMD were enrolled in a prospective SS-OCT study, and the onset of large hyperTDs was retrospectively analyzed. Imaging was performed using 6 × 6 mm SS-OCT angiography (SS-OCTA) scans at baseline and follow-up. Large hyperTDs were defined as bright lesions ≥250 µm in greatest linear dimension (GLD) on en face sub-retinal pigment epithelium (subRPE) slabs positioned 64 to 400 µm beneath Bruch's membrane (BM). CaD were identified as drusen with heterogeneous internal reflectivity projecting choroidal hypotransmission defects (hypoTDs) on the same subRPE slabs. CaD were distinguished from hyperreflective foci (HRF) by analyzing corresponding B-scans. Two independent graders used a semiautomated algorithm to refine CaD outlines and reach consensus, with disagreements adjudicated by a senior grader. CaD area, HRF area, and drusen volume were measured within 5-mm fovea-centered circles.
Median follow-up time for the 171 eyes from 121 patients followed in this study was 59.1 months (95% CI: 52.0-67.8 months), and 82 eyes developed at least one large hyperTD during follow-up. The mean baseline CaD area measurement was 0.037 mm² [range: 0-0.567 mm²] in eyes that developed hyperTDs, while in eyes that did not, it was 0.008 mm² [range: 0-0.360 mm²] (P = .01). Drusen volume, HRF area, and CaD area were predictors for hyperTD onset when considered alone, but only HRF area (P < .001) and CaD area (P =.008) remained significant predictors for hyperTD onset when using a multivariable Cox regression analysis. Regardless of area, the presence of any CaD increased the risk of hyperTD formation (P < .001).
In a multivariable Cox regression analysis, the area measurements of CaD and HRF in eyes with iAMD were significant predictors of hyperTD onset, and the presence of any CaD increased the risk of hyperTD formation.
本研究采用正面扫频源光学相干断层扫描(SS-OCT)成像技术,对存在和不存在钙化性玻璃膜疣(CaD)的中度年龄相关性黄斑变性(iAMD)患者的眼睛进行随访,以确定CaD的存在和大小是否会增加形成大的脉络膜高透过缺陷(hyperTDs)的风险。
一项前瞻性队列研究的事后亚组分析。
将患有iAMD的眼睛纳入一项前瞻性SS-OCT研究,并对大hyperTDs的发病情况进行回顾性分析。在基线和随访时使用6×6mm的SS-OCT血管造影(SS-OCTA)扫描进行成像。大hyperTDs被定义为在位于Bruch膜(BM)下方64至400μm的正面视网膜色素上皮(subRPE)平板上,最大线性尺寸(GLD)≥250μm的明亮病变。CaD被识别为在同一subRPE平板上具有不均匀内部反射率并投射脉络膜低透过缺陷(hypoTDs)的玻璃膜疣。通过分析相应的B扫描将CaD与高反射灶(HRF)区分开来。两名独立的分级人员使用半自动算法细化CaD轮廓并达成共识,如有分歧则由一名高级分级人员裁决。在以黄斑为中心的5mm圆内测量CaD面积、HRF面积和玻璃膜疣体积。
本研究中随访的121例患者的171只眼睛的中位随访时间为59.1个月(95%CI:52.0 - 67.8个月),82只眼睛在随访期间出现了至少一个大的hyperTDs。出现hyperTDs的眼睛的平均基线CaD面积测量值为0.037mm²[范围:0 - 0.567mm²],而未出现的眼睛为0.008mm²[范围:0 - 0.360mm²](P = 0.01)。单独考虑时,玻璃膜疣体积、HRF面积和CaD面积是hyperTDs发病的预测因素,但在使用多变量Cox回归分析时,只有HRF面积(P < 0.001)和CaD面积(P = 0.008)仍然是hyperTDs发病的确切预测因素。无论面积大小,任何CaD的存在都会增加hyperTDs形成的风险(P < 0.001)。
在多变量Cox回归分析中,iAMD患者眼睛中CaD和HRF的面积测量是hyperTDs发病的重要预测因素,任何CaD的存在都会增加hyperTDs形成的风险。