Retinal and Visual Pathways Involvement in Carriers of Friedreich’s Ataxia

• Published in: Diagnostics (Basel) Vol. 12; no. 12; p. 3135
• Main Authors: Ziccardi, Lucia, Barbano, Lucilla, Antonelli, Giulio, Cioffi, Ettore, Di Renzo, Antonio, Gioiosa, Valeria, Marcotulli, Christian, Grzybowski, Andrzej, Casali, Carlo, Parisi, Vincenzo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.12.2022; MDPI
• Subjects: Ataxia; Cardiomyopathy; carriers; Development and progression; Diabetes; Diabetic retinopathy; Disease; Dysarthria; ERG; Families & family life; Friedreich; Friedreich's ataxia; Health aspects; Hearing loss; mfERG; Morphology; Nervous system diseases; Optic nerve; Oxidative stress; Retina; VEP; Visual acuity; Visual perception; Italy; VEP; OCT; ataxia; Friedreich; carriers; ERG; mfERG; PERG
• ISSN: 2075-4418; 2075-4418
• DOI: 10.3390/diagnostics12123135

Friedreich’s ataxia (FRDA) is a rare autosomal recessive neurodegenerative disorder due to the homozygous pathological expansion of guanine-adenine-adenine (GAA) triplet repeats in the first intron of the FXN gene, which encodes for the mitochondrial protein frataxin. In the visual system, the typical manifestations are ocular motility abnormality, optic neuropathy, and retinopathy. Despite the evidence of ophthalmological impairment in FRDA patients, there is a lack of information about the morpho-functional condition of the retina and of the optic pathways in healthy heterozygous carriers of Friedreich’s ataxia (C-FRDA). Ten C-FRDA subjects (providing 20 eyes) and thirty-five Controls (providing 70 eyes) underwent a complete neurological and ophthalmological examination comprehensive of functional (full-field Electroretinogram (ffERG), multifocal Electroretinogram (mfERG), Visual Evoked Potential (VEP), and Pattern Reversal Electroretinogram (PERG)) and morphological assessments (Optical Coherence Tomography, OCT) of the retina, macula, retinal ganglion cells, and visual pathways. The groups’ data were compared using a two-sample t-test. Pearson’s test was used to investigate the morpho-functional correlations. Statistically significant differences (p < 0.01) between C-FRDA and Control eyes for the values of the following parameters were found: ffERG b-wave amplitude, mfERG Response Amplitude Densities, PERG P50 implicit time and P50-N95 amplitude, VEP P100 implicit time, Retinal Nerve Fiber Layer (RNFL) Overall, and Nasal thickness. The values of the OCT macular volume were not statistically different (p > 0.01) between the two Groups. Therefore, our data suggest that, in C-FRDA, a dysfunction of retinal elements without morphological macular impairment may occur. In addition, a morphological impairment of RNFL associated with an abnormal neural conduction along the visual pathways can be also detected.