Abstract

Visual evoked potentials (VEP) are changes in potentials that arise in the central nervous system. In the interpretation of the VEP test results, it is assumed that the elongation of the latency time is caused by the demyelination of the nerve fibers, and the axon damage is responsible for the decrease in the amplitude. The observed VEP deviations are not specific for specific diseases, but indicate disturbances in visual conductivity. VEP may play a diagnostic role in the early detection of visual involvement. The aim of the study was the functioning of visual pathway assessment on the basis of visual evoked potentials (VEP) examination, in patients with primary Sjögren’s Syndrome (pSS), without focal symptoms of central nervous system disorder. The effect of disease activity, as assessed by clinical parameters and antibody levels (anti-Ro52, SSA, and SSB), on the central nervous system was also evaluated. Thirty-two consecutive patient with pSS (31 females, 1 male) were included in the study. VEP was performed at baseline, and after 6 (T6) years. Their results were compared longitudinally between the baseline and T6, depending on the duration of the disease and treatment. The immunological activity of pSS was also analyzed. The group of patients showed a significant prolongation of the P100 implicit time (105.5 ± 5.1 vs. 100.6 ± 3.9; p = 0.000) and a significant higher the P100-N145 amplitude (12.3 ± 4.1 vs. 9.4 ± 3.0; p = 0.000). Abnormalities in electrophysiological parameters of VEP at baseline correlated with presentation of anti-Ro52 antibodies and aching joints. At baseline, the P100 implicit time was shorter for the patients with pSS than for those at T6 (105.50 ± 5.1 vs. 109.37 ± 5.67; p = 0.002). pSS patients without CNS involvement presented with dysfunction of visual pathway, as revealed by VEP abnormalities. Relationships were found between VEP parameters and with present of anti-Ro52 antibodies and aching joints. VEP may be a useful method for assessment and monitoring of subclinical visual deficit in the course of pSS.

Highlights

  • The analysis enables the detection of even subclinical disorders, in the case of visual evoked potentials (VEP), in the optic pathway

  • The first symptoms of primary Sjögren’s Syndrome (pSS) observed in patients were: xerophthalmia/xerostomia (63%), fatigue

  • Conclusions pSS patients without CNS involvement presented with dysfunction of visual pathway, as revealed by VEP abnormalities

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Summary

Introduction

Primary Sjögren’s Syndrome (pSS) is a chronic, systemic autoimmune disease that occurs in 2–3% of the adult population [1,2,3,4]. The pSS pathomechanism is based on humoral and cellular response disorders, the symptoms spectrum may be broad and include organic disorders such as muscles, eyes, and the nervous system. As suggested in the available reference literature, patients with pSS the damage to the sight organ and/or the visual pathway may anticipate axial pSS symptoms. It may appear in cases with established diagnoses and a longer course of the disease [5,6]

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