Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France; CHNO des Quinze-Vingts, Centre de Référence Maladies Rares REFERET and DHU Sight Restore, INSERM-DGOS CIC1423, Paris, France; Department of Ophthalmology, IRCCS San Raffaele Hospital, Milan, Italy.
Sorbonne Université, INSERM, CNRS, Institut de la Vision, Paris, France.
Ophthalmology. 2024 Oct;131(10):1175-1184. doi: 10.1016/j.ophtha.2024.04.001. Epub 2024 Apr 6.
To describe the clinical outcome and late-stage findings of extensive macular atrophy with pseudodrusen-like appearance (EMAP).
Retrospective cohort study.
Seventy-eight patients (156 eyes) affected by EMAP.
We collected data on best-corrected visual acuity, kinetic perimetry, OCT, short-wavelength autofluorescence, and near-infrared autofluorescence findings. Genetic testing for the TIMP3 and C1QTNF5 genes was performed via Sanger sequencing for 58 patients, with no pathogenic variants identified.
The primary outcomes were best-corrected visual acuity at the last examination, visual field at the last examination, and incidence rates and time-to-event curves for blindness with the United States Social Security Administration and World Health Organization (WHO) criteria, foveal involvement, and atrophy enlargement beyond the 30° and 55° field of view. Imaging findings at the last examination were secondary outcomes.
At the most recent visit, mean age was 70.9 ± 5.2 years. Using United States criteria, 58.1% of the patients were blind, and 25.8% were blind according to WHO criteria. All eyes showed large central scotomas, which were associated with visual field constriction in 22.2% of eyes. We detected focal openings or large dehiscences of Bruch's membrane (BM) in 25.4% of eyes. Near-infrared autofluorescence showed increased visibility of the choroidal vessels beyond the atrophy in 87.2% of eyes. The incidence rates for blindness were 3.95 per 100 patient-years with United States criteria and 1.54 per 100 patient-years according to WHO criteria. The incidence rates were 22.8 per 100 eye-years for foveal involvement, 12.0 per 100 eye-years for atrophy enlargement beyond 30°, and 6.6 per 100 eye-years for atrophy enlargement beyond 55°. The estimates were not influenced by the age at onset.
We identified characteristic imaging findings, including BM ruptures, in elder patients with EMAP and calculated incidence rates for different functional and anatomic outcomes.
FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
描述假性小体样广泛黄斑萎缩(EMAP)的临床结果和晚期发现。
回顾性队列研究。
78 名(156 只眼)患有 EMAP 的患者。
我们收集了最佳矫正视力、运动视野计、OCT、短波自动荧光和近红外自动荧光检查结果的数据。对 58 名患者进行了 TIMP3 和 C1QTNF5 基因的遗传检测,通过 Sanger 测序未发现致病性变异。
主要结局是最后一次检查时的最佳矫正视力、最后一次检查时的视野和美国社会保障局和世界卫生组织(WHO)标准下的失明发生率和时间曲线、中心凹受累以及视野 30°和 55°以外的萎缩扩大。最后一次检查的影像学发现为次要结局。
在最近一次就诊时,平均年龄为 70.9±5.2 岁。根据美国标准,58.1%的患者失明,25.8%的患者根据世卫组织标准失明。所有眼睛均显示大的中心暗点,其中 22.2%的眼睛与视野收缩相关。我们在 25.4%的眼睛中检测到脉络膜膜(BM)的局灶性开口或大裂孔。近红外自发荧光显示 87.2%的眼睛中脉络膜血管的可见度增加,超过了萎缩区。根据美国标准,失明的发生率为每 100 患者年 3.95 例,根据世卫组织标准为每 100 患者年 1.54 例。中心凹受累的发生率为每 100 眼年 22.8 例,30°以外的萎缩扩大发生率为每 100 眼年 12.0 例,55°以外的萎缩扩大发生率为每 100 眼年 6.6 例。这些估计值不受发病年龄的影响。
我们在患有 EMAP 的老年患者中发现了特征性的影像学表现,包括 BM 破裂,并计算了不同功能和解剖结果的发生率。
本文末尾的脚注和披露中可能包含专有或商业披露信息。