Centre for Ophthalmology and Visual Science, The University of Western Australia, Nedlands, Western Australia, Australia.
Ocular Tissue Engineering Laboratory, Lions Eye Institute, Nedlands, Western Australia, Australia.
Invest Ophthalmol Vis Sci. 2023 Jan 3;64(1):3. doi: 10.1167/iovs.64.1.3.
Female carriers of RPGR mutations demonstrate no significant retinal dysfunction or structural change despite a characteristic tapetal-like reflex. In this study, we examined localized changes of pointwise sensitivity (PWS) and cone density (CD) using microperimetry (MP) and adaptive optics (AO) imaging in female carriers of RPGR mutations.
In this cross-sectional case-control study, MP (MAIA, 10-2 test grid) and AO imaging (rtx1) were performed in female carriers of RPGR mutations and unrelated age-matched healthy controls. PWS at 68 loci located 1 degree to 9 degrees away from the preferred retinal locus and CD at 12 loci located 1 degree to 3 degrees away from the foveal center were measured. Severity of defect was defined by standard deviation (SD) from age-matched healthy control means: normal (<1 SD from normal average), moderate defect (1-2 SD from normal average), and severe defect (>2 SD from normal average).
Twelve patients from seven unrelated families were enrolled. Seven patients were asymptomatic, 5 of whom had visual acuity 20/20 or better in both eyes. PWS and CD were available in 12 and 8 patients, respectively. Severe PWS and CD defect in at least 1 test location was observed in 10 of 12 patients and 7 of 8 patients, respectively. Among the five asymptomatic patients who had normal visual acuity, severe PWS and CD defects were observed in three of five and four of five patients, respectively.
MP and AO imaging revealed early functional and structural changes in asymptomatic RPGR mutation carriers and should be considered in clinical assessment of these patients.
尽管女性 RPGR 突变携带者表现出典型的光斑样反射,但她们的视网膜功能或结构没有明显异常。在这项研究中,我们使用微视野计(MP)和自适应光学(AO)成像检查了 RPGR 突变女性携带者的局部点敏感性(PWS)和锥体细胞密度(CD)的变化。
在这项横断面病例对照研究中,对 RPGR 突变的女性携带者和无相关年龄匹配的健康对照者进行了 MP(MAIA,10-2 测试网格)和 AO 成像(rtx1)检查。在距优势视网膜位置 1 度至 9 度的 68 个位置测量 PWS,在距中心凹 1 度至 3 度的 12 个位置测量 CD。通过与年龄匹配的健康对照组平均值的标准差(SD)定义缺陷的严重程度:正常(正常平均值的 1 SD 以内)、中度缺陷(正常平均值的 1-2 SD)和严重缺陷(正常平均值的 2 SD 以上)。
纳入了来自七个无关家庭的 12 名患者。七名患者无症状,其中五名双眼视力均为 20/20 或更好。分别有 12 名患者和 8 名患者可获得 PWS 和 CD。在 12 名患者中,有 10 名患者在至少一个测试位置观察到严重的 PWS 和 CD 缺陷,在 8 名患者中,有 7 名患者观察到严重的 PWS 和 CD 缺陷。在五名无症状且视力正常的患者中,分别有 3 名和 4 名患者在 5 名患者中观察到严重的 PWS 和 CD 缺陷。
MP 和 AO 成像显示无症状 RPGR 突变携带者的早期功能和结构变化,在对这些患者进行临床评估时应考虑这些变化。