Ziccardi Lucia, Barbano Lucilla, Boffa Laura, Albanese Maria, Nicoletti Carolina Gabri, Landi Doriana, Grzybowski Andrzej, Falsini Benedetto, Marfia Girolama Alessandra, Centonze Diego, Parisi Vincenzo
IRCCS-Fondazione Bietti, Via Livenza 1, 00198 Rome, Italy.
Unit of Neurology, Fondazione Policlinico Tor Vergata, Via Oxford 81, 00133 Rome, Italy.
J Clin Med. 2020 Nov 22;9(11):3766. doi: 10.3390/jcm9113766.
The involvement of macular preganglionic elements' function, during the neurodegenerative process of multiple sclerosis (MS), is controversial. In this case-control observational and retrospective study, we assessed multifocal electroretinogram (mfERG) responses from 41 healthy Controls, 41 relapsing-remitting MS patients without optic neuritis (ON) (MS-noON Group) and 47 MS patients with ON: 27 with full recovery of high-contrast best corrected visual acuity (BCVA) (MS-ON-G Group) and 20 with poor recovery (between 0.2 and 1 LogMAR) of BCVA, (MS-ON-P Group). In the latter Group, Sd-OCT macular volumes and thicknesses of whole and inner and outer retina were measured. MfERG N1 and P1 implicit times (ITs), and N1-P1 response amplitude densities (RADs), were measured from concentric rings (R) with increasing foveal eccentricity: 0-5° (R1), 5-10° (R2), 10-15° (R3), 15-20° (R4), 20-25° (R5), and from retinal sectors (superior, nasal, inferior and temporal) between 0-15° and 0-25°. In the MS-ON-P Group, mean mfERG RADs detected from R1 (0-5°) and from the central nasal sector (0-15°) were significantly reduced ( < 0.01) with respect to those of the Control, MS-noON and MS-ON-G Groups. No other significant differences between Groups for any mfERG parameters were found. All Sd-OCT measurements, apart from the inner retina macular volume in the central 1 mm, were significantly reduced in MS-ON-P patients compared to Controls. The functional impairment in the MS-ON-P Group was associated but not correlated with structural changes of the outer and inner retinal layers in corresponding retinal Areas and Sectors. Our results suggest that in MS, exclusively after ON with poor recovery of BCVA, the neurodegenerative process can induce dysfunctional mechanisms involving photoreceptors and bipolar cells of the fovea and of the more central nasal macular area.
在多发性硬化症(MS)的神经退行性变过程中,黄斑节前神经元功能的参与情况存在争议。在这项病例对照观察性回顾研究中,我们评估了41名健康对照者、41名无视神经炎(ON)的复发缓解型MS患者(MS-noON组)以及47名患有ON的MS患者的多焦视网膜电图(mfERG)反应:27名高对比度最佳矫正视力(BCVA)完全恢复的患者(MS-ON-G组)和20名BCVA恢复较差(0.2至1 LogMAR之间)的患者(MS-ON-P组)。在后者组中,测量了黄斑区的扫描光相干断层扫描(Sd-OCT)体积以及整个视网膜、视网膜内层和外层的厚度。从中心凹偏心度逐渐增加的同心环(R):0 - 5°(R1)、5 - 10°(R2)、10 - 15°(R3)、15 - 20°(R4)、20 - 25°(R5),以及0 - 15°和0 - 25°之间的视网膜象限(上、鼻、下和颞侧)测量mfERG的N1和P1隐时(ITs)以及N1 - P1反应振幅密度(RADs)。在MS-ON-P组中,从R1(0 - 5°)和中央鼻侧象限(0 - 15°)检测到的mfERG平均RADs相对于对照组、MS-noON组和MS-ON-G组显著降低(<0.01)。在任何mfERG参数方面,各组之间未发现其他显著差异。与对照组相比,MS-ON-P患者除中央1mm内视网膜黄斑体积外的所有Sd-OCT测量值均显著降低。MS-ON-P组的功能损害与相应视网膜区域和象限中外层和内层视网膜层的结构变化相关,但无相关性。我们的结果表明,在MS中,仅在ON后且BCVA恢复较差时,神经退行性变过程可诱导涉及中央凹和更中央鼻侧黄斑区的光感受器和双极细胞的功能障碍机制。