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Progressive retinal structure abnormalities in multiple system atrophy
Author(s) -
MendozaSantiesteban Carlos E.,
Palma JoseAlberto,
Martinez Jose,
NorcliffeKaufmann Lucy,
Hedges Thomas R.,
Kaufmann Horacio
Publication year - 2015
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.26360
Subject(s) - nerve fiber layer , retinal , medicine , atrophy , ganglion , asymptomatic , ophthalmology , nerve fiber , biomarker , retinal ganglion cell , optical coherence tomography , visual acuity , pathology , anatomy , biology , biochemistry
Background Objective measures of disease progression that can be used as endpoints in clinical trials of MSA are necessary. We studied retinal thickness in patients with MSA and assessed changes over time to determine its usefulness as an imaging biomarker of disease progression. Methods This was a cross‐sectional study including 24 patients with MSA, 20 with PD, and 35 controls, followed by a longitudinal study of 13 MSA patients. Patients were evaluated with high‐definition optical coherence tomography and the Unified Multiple System Atrophy Rating Scale. Evaluations were performed at baseline and at consecutive follow‐up visits for up to 26 months. Results MSA subjects had normal visual acuity and color discrimination. Compared to controls, retinal nerve fiber layer ( P = 0.008 and P = 0.001) and ganglion cell complex ( P = 0.013 and P = 0.001) thicknesses were reduced in MSA and PD. No significant differences between MSA and PD were found. Over time, in patients with MSA, there was a significant reduction of the retinal nerve fiber layer and ganglion cell complex thicknesses, with estimated annual average losses of 3.7 and 1.8 μm, respectively. Conclusions Visually asymptomatic MSA patients exhibit progressive reductions in the thickness of the retinal nerve fiber layer and, to a lesser extent, in the macular ganglion cell complex, which can be quantified by high‐definition optical coherence tomography. Specific patterns of retinal nerve fiber damage could be a useful imaging biomarker of disease progression in future clinical trials. © 2015 International Parkinson and Movement Disorder Society