Multifocal visual evoked potentials and contrast sensitivity correlate with ganglion cell-inner plexiform layer thickness in multiple sclerosis
•MfVEP amplitude is more highly correlated with GCIPL than RNFL thickness in ON.•GCIPL is a strong structural biomarker for optic nerve degeneration in RRMS.•MfVEP is more sensitive than OCT in detecting subclinical defects in non-ON. To examine the relationship between optical coherence tomography...
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Veröffentlicht in: | Clinical neurophysiology 2019-01, Vol.130 (1), p.180-188 |
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Sprache: | eng |
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Zusammenfassung: | •MfVEP amplitude is more highly correlated with GCIPL than RNFL thickness in ON.•GCIPL is a strong structural biomarker for optic nerve degeneration in RRMS.•MfVEP is more sensitive than OCT in detecting subclinical defects in non-ON.
To examine the relationship between optical coherence tomography (OCT) macular ganglion cell-inner plexiform layer thickness (GCIPLT), peripapillary retinal nerve fiber layer thickness (RNFLT) and visual function in relapsing-remitting multiple sclerosis (RRMS).
Cirrus OCT, VERIS 60-sector multifocal visual evoked potential (mfVEP) and Pelli-Robson contrast sensitivity (CS) were obtained for 53 eyes with last optic neuritis (ON) > 6 months and 105 non-ON eyes in 90 patients. One eye (43 ON, 73 non-ON) was used for correlations when both had the same history. Global (G, 60 sectors) and central 5.6° (C, 24 sectors) mfVEP amplitude and latency were calculated as mean logSNR and median latency.
Eyes showing abnormal mfVEP (amplitude or latency) vs OCT (GCIPLT or RNFLT) was 77% vs 69% (p = 0.33) in ON, 45% vs 22% (p |
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ISSN: | 1388-2457 1872-8952 |
DOI: | 10.1016/j.clinph.2018.10.007 |