Ronzina I A, Sheremet N L, Zhorzholadze N V
Krasnov Research Institute of Eye Diseases, Moscow, Russia.
Vestn Oftalmol. 2022;138(6):44-54. doi: 10.17116/oftalma202213806144.
Retinitis pigmentosa (RP) is an inherited disease associated with various genetic mutations. Developments in the field of genetic engineering give relevance to the search for methods of studying retinal function, which can prove informative in the selection of patients for treatment.
To evaluate the information content of multifocal electroretinography (mfERG) in the diagnostics of the functional state of the central retina in retinitis pigmentosa (RP).
The study included 115 patients (228 eyes) with PR and 15 people (30 eyes) who comprised the control group. All subjects underwent standard ophthalmological examination, computer perimetry, color vision study, retinal spectral optical coherence tomography, ganzfeld electroretinography (gERG) and mfERG. The relationship between mfERG parameters and the degree of gERG changes, as well as various functional and morphological parameters of the retina was assessed.
Visual acuity and perimetry indices varied over a wide range. GERG was unrecordable in 50.4% of cases. MfERG was registered in 214 (98.3%) eyes with varying degrees of change in visual acuity, visual field and gERG parameters. A medium degree positive relationship was revealed between the biopotential density of the retina in the foveal and parafoveal zones and visual acuity (=0.68; 0.63), a high degree - between the density of ttotal biopotential of the central retina (DValue) and the average light sensitivity (=0.9), a weak degree - between DValue and the thickness and volume of the peripheral retina (=0.37; 0.42), a medium negative correlation was found between the average defect in light sensitivity and the biopotential density in the periphery (Rings 4-5) on mfERG, DValue (= -0.67; -0.65; -0.69).
MfERG detects retinal dysfunctions at an early stage of RP, in eyes with high visual acuity, normal parameters of the central visual field and gERG, as well as in low visual acuity, a pronounced decrease in light sensitivity, unrecordable gERG. MfERG can be informative in the selection of patients with RP for gene therapy.
视网膜色素变性(RP)是一种与多种基因突变相关的遗传性疾病。基因工程领域的发展使得寻找研究视网膜功能的方法具有重要意义,这在选择治疗患者时可能具有参考价值。
评估多焦视网膜电图(mfERG)在视网膜色素变性(RP)患者中央视网膜功能状态诊断中的信息含量。
研究包括115例RP患者(228只眼)和15名对照者(30只眼)。所有受试者均接受标准眼科检查、电脑视野检查、色觉检查、视网膜光谱光学相干断层扫描、全视野视网膜电图(gERG)和mfERG检查。评估mfERG参数与gERG变化程度以及视网膜各种功能和形态学参数之间的关系。
视力和视野指数变化范围广泛。50.4%的病例gERG无法记录。mfERG在214只(98.3%)眼中记录到,这些眼的视力、视野和gERG参数有不同程度的变化。在黄斑区和旁黄斑区视网膜的生物电位密度与视力之间显示出中度正相关(=0.68;0.63),高度正相关——在中央视网膜总生物电位密度(D值)与平均光敏感度之间(=0.9),弱度正相关——在D值与周边视网膜的厚度和体积之间(=0.37;0.42),在mfERG上,光敏感度平均缺陷与周边(第4 - 5环)生物电位密度之间发现中度负相关,D值(= -0.67; -0.65; -0.69)。
mfERG可在RP的早期阶段检测到视网膜功能障碍,包括视力正常、中央视野和gERG参数正常的眼睛,以及视力低下、光敏感度明显降低、gERG无法记录的眼睛。mfERG在选择RP患者进行基因治疗时可能具有参考价值。