Optical coherence tomography in multiple sclerosis: A 3‐year prospective multicenter study

Objective To evaluate changes over 3 years in the thickness of inner retinal layers including the peripapillary retinal nerve fiber layer (pRNFL), and combined macular ganglion cell and inner plexiform layers (mGCIPL), in individuals with relapsing‐remitting multiple sclerosis (RRMS) versus healthy...

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Veröffentlicht in:Annals of clinical and translational neurology 2021-12, Vol.8 (12), p.2235-2251
Hauptverfasser: Paul, Friedemann, Calabresi, Peter A., Barkhof, Frederik, Green, Ari J., Kardon, Randy, Sastre‐Garriga, Jaume, Schippling, Sven, Vermersch, Patrick, Saidha, Shiv, Gerendas, Bianca S., Schmidt‐Erfurth, Ursula, Agoropoulou, Catherine, Zhang, Ying, Seifer, Gustavo, Petzold, Axel
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Sprache:eng
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Zusammenfassung:Objective To evaluate changes over 3 years in the thickness of inner retinal layers including the peripapillary retinal nerve fiber layer (pRNFL), and combined macular ganglion cell and inner plexiform layers (mGCIPL), in individuals with relapsing‐remitting multiple sclerosis (RRMS) versus healthy controls; to determine whether optical coherence tomography (OCT) is sufficiently sensitive and reproducible to detect small degrees of neuroaxonal loss over time that correlate with changes in brain volume and disability progression as measured by the Expanded Disability Status Scale (EDSS). Methods Individuals with RRMS from 28 centers (n = 333) were matched with 64 healthy participants. OCT scans were performed on Heidelberg Spectralis machines (at baseline; 1 month; 6 months; 6‐monthly thereafter). Results OCT measurements were highly reproducible between baseline and 1 month (intraclass correlation coefficient >0.98). Significant inner retinal layer thinning was observed in individuals with multiple sclerosis (MS) compared with controls regardless of previous MS‐associated optic neuritis––group differences (95% CI) over 3 years: pRNFL: −1.86 (−2.54, −1.17) µm; mGCIPL: −2.03 (−2.78, −1.28) µm (both p 
ISSN:2328-9503
2328-9503
DOI:10.1002/acn3.51473