Song Hongxin, Latchney Lisa, Williams David, Chung Mina
Center for Visual Science, University of Rochester, Rochester, New York.
Flaum Eye Institute, University of Rochester, Rochester, New York.
JAMA Ophthalmol. 2014 Sep;132(9):1099-104. doi: 10.1001/jamaophthalmol.2014.1079.
Fundus albipunctatus (FA) is a form of congenital stationary night blindness characterized by yellow-white spots, which were classically described as subretinal. Although night blindness and delayed dark adaptation are hallmarks of this condition, recent studies have described a macular phenotype, particularly among older patients. Using a fluorescence adaptive optics scanning laser ophthalmoscope (FAOSLO), this study provides in vivo morphologic data at the cellular level in FA.
To study the cone photoreceptors and the albipunctate spots in FA at single-cell resolution.
DESIGN, SETTING, AND PARTICIPANT: A woman in her 30s with FA underwent a complete ophthalmic examination, including conventional imaging tests, at the University of Rochester. A FAOSLO was used to obtain infrared reflectance images of the cone mosaic at the central fovea and along the superior and temporal meridians to 10° eccentricity. Cone density was measured at the foveal center, and cone spacing was calculated in sampling windows eccentrically. In the area of the albipunctate spots, autofluorescence FAOSLO images (excitation, 561 nm; emission, 624 Δ 40 nm) were simultaneously obtained.
Structural appearance of cones, cone density and spacing, and reflectance and autofluorescence of albipunctate spots.
Cone density was reduced to 70% of the lower limit of the normal range at the foveal center (78.7 × 10(3) cones/mm(2); mean [SD] reference range, 199 [87] × 10(3) cones/mm(2)), and cone spacing was increased eccentrically to 10° (sign test, P = .045). Individual cone central core reflectances appeared dim, suggesting loss of photoreceptor outer segments. The albipunctate spots were hypoautofluorescent. No photoreceptors or retinal pigment epithelium cells were identified at the locations of the albipunctate spots.
Although the predominant clinical symptom of night blindness and the electroretinography results suggest a primary rod dysfunction, examination with a FAOSLO demonstrates that cone density is also reduced. This finding may represent an early sign of progression to macular phenotype in FA. The hypoautofluorescence suggests that the albipunctate spots do not represent lipofuscin.
白点状眼底(FA)是先天性静止性夜盲的一种形式,其特征为黄白色斑点,传统上被描述为视网膜下斑点。尽管夜盲和暗适应延迟是这种疾病的标志,但最近的研究描述了一种黄斑表型,尤其是在老年患者中。本研究使用荧光自适应光学扫描激光检眼镜(FAOSLO),在细胞水平上提供了FA的体内形态学数据。
以单细胞分辨率研究FA中的视锥光感受器和白点状斑点。
设计、地点和参与者:一名30多岁患有FA的女性在罗切斯特大学接受了包括传统成像检查在内的全面眼科检查。使用FAOSLO获取中央凹以及沿上和颞侧子午线至10°偏心度处视锥镶嵌的红外反射图像。在中央凹中心测量视锥密度,并在偏心采样窗口中计算视锥间距。在白点状斑点区域,同时获取自发荧光FAOSLO图像(激发波长561nm;发射波长624±40nm)。
视锥的结构外观、视锥密度和间距,以及白点状斑点的反射率和自发荧光。
中央凹中心的视锥密度降至正常范围下限的70%(78.7×10³个视锥/mm²;平均值[标准差]参考范围为199[87]×10³个视锥/mm²),视锥间距在偏心至10°时增加(符号检验,P = 0.045)。单个视锥中央核心反射率显得暗淡,提示光感受器外段缺失。白点状斑点自发荧光减弱。在白点状斑点位置未识别到光感受器或视网膜色素上皮细胞。
尽管夜盲这一主要临床症状和视网膜电图结果提示原发性视杆功能障碍,但FAOSLO检查显示视锥密度也降低。这一发现可能代表FA向黄斑表型进展的早期迹象。自发荧光减弱表明白点状斑点不代表脂褐素。