Impaired motion perception is associated with functional and structural visual pathway damage in multiple sclerosis and neuromyelitis optica spectrum disorders

被引:3
|
作者
Ayadi, Noah [1 ,2 ,3 ,4 ,5 ]
Oertel, Frederike C. [1 ,2 ,3 ,4 ,5 ,6 ]
Asseyer, Susanna [1 ,2 ,3 ,4 ,5 ]
Rust, Rebekka [1 ,2 ,3 ,4 ,5 ]
Duchow, Ankelien [1 ,2 ,3 ,4 ,5 ]
Kuchling, Joseph [1 ,2 ,3 ,4 ,5 ,7 ]
Bellmann-Strobl, Judith [1 ,2 ,3 ,4 ,5 ]
Ruprecht, Klemens [3 ,4 ,7 ]
Klistorner, Alexander [8 ,9 ]
Brandt, Alexander U. [1 ,2 ,3 ,4 ,5 ,10 ]
Paul, Friedemann [1 ,2 ,3 ,4 ,5 ,7 ]
Zimmermann, Hanna G. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Max Delbruck Ctr Mol Med, Expt & Clin Res Ctr, Berlin, Germany
[2] Charite Univ Med Berlin, Berlin, Germany
[3] Free Univ Berlin, Berlin, Germany
[4] Humboldt Univ, Berlin, Germany
[5] Charite Univ Med Berlin, NeuroCure Clin Res Ctr, Berlin, Germany
[6] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[7] Charite Univ Med Berlin, Dept Neurol, Berlin, Germany
[8] Macquarie Univ, Fac Med Hlth & Human Sci, Sydney, NSW, Australia
[9] Univ Sydney, Save Sight Inst, Sydney, NSW, Australia
[10] Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
关键词
Multiple sclerosis; neuromyelitis optica spectrum disorders; motion perception; retina; vision disorders; optical coherence tomography; visual evoked potentials; COGNITIVE IMPAIRMENT; TEMPORAL ASPECTS; NEURITIS; GLAUCOMA; SPEED;
D O I
10.1177/13524585211032801
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Decreased motion perception has been suggested as a marker for visual pathway demyelination in optic neuritis (ON) and/or multiple sclerosis (MS). Objectives: To examine the influence of neuro-axonal damage on motion perception in MS and neuromyelitis optica spectrum disorders (NMOSD). Methods: We analysed motion perception with numbers-from-motion (NFM), visual acuity, (multifocal (mf)) VEP, optical coherence tomography in patients with MS (n = 38, confirmatory cohort n = 43), NMOSD (n = 13) and healthy controls (n = 33). Results: NFM was lower compared with controls in MS (B = -12.37, p < 0.001) and NMOSD (B = -34.5, p < 0.001). NFM was lower in ON than in non-ON eyes (B = -30.95, p = 0.041) in NMOSD, but not MS. In MS and NMOSD, lower NFM was associated with worse visual acuity (B = -139.4, p < 0.001/B = -77.2, p < 0.001) and low contrast letter acuity (B = 0.99, p = 0.002/B = 1.6, p < 0.001), thinner peripapillary retinal nerve fibre layer (B = 1.0, p < 0.001/ B = 0.92, p = 0.016) and ganglion cell/inner plexiform layer (B = 64.8, p < 0.001/B = 79.5, p = 0.006), but not with VEP P100 latencies. In the confirmatory MS cohort, lower NFM was associated with thinner retinal nerve fibre layer (B = 1.351, p < 0.001) and increased mfVEP P100 latencies (B = -1.159, p < 0.001). Conclusions: Structural neuro-axonal visual pathway damage is an important driver of motion perception impairment in MS and NMOSD.
引用
收藏
页码:757 / 767
页数:11
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