Spinal cord and infratentorial lesions in radiologically isolated syndrome are associated with decreased retinal ganglion cell/inner plexiform layer thickness
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作者:
Filippatou, Angeliki
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Johns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USAJohns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USA
Filippatou, Angeliki
[1
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Shoemaker, Thomas
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Johns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USAJohns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USA
Shoemaker, Thomas
[1
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Esch, Megan
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Johns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USAJohns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USA
Esch, Megan
[1
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Qutab, Madiha
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Johns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USAJohns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USA
Qutab, Madiha
[1
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Gonzalez-Caldito, Natalia
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Johns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USAJohns Hopkins Univ, Sch Med, Dept Neurol, Div Neuroimmunol & Neurol Infect, 600 N Wolfe St, Baltimore, MD 21287 USA
Background: The role of retinal imaging with optical coherence tomography (OCT) in assessing individuals with radiologically isolated syndrome (RIS) remains largely unexplored. Objective: To assess retinal layer thicknesses in RIS and examine their associations with clinical features suggestive of increased risk for conversion to multiple sclerosis (MS). Methods: A total of 30 RIS subjects and 60 age- and sex-matched healthy controls (HC) underwent retinal imaging with spectral-domain OCT, followed by automated segmentation of retinal layers. Results: Overall, retinal layer thicknesses did not differ between RIS and HC. However, RIS subjects with spinal cord (SC) lesions had lower ganglion cell+inner plexiform layer (GCIP) thickness compared to HC (-4.41 mu m; p=0.007) and RIS without SC lesions (-3.53 mu m; p=0.041). Similarly, RIS subjects with infratentorial (IT) brain lesions had lower GCIP thickness compared to HC (-4.07 mu m; p<0.001) and RIS without IT lesions (-3.49 mu m; p=0.029). Multivariate analyses revealed that the presence of SC or IT lesions were independently associated with lower GCIP thickness in RIS (p=0.04 and p=0.03, respectively). Other patient characteristics, including sex, abnormal cerebrospinal fluid, and presence of gadolinium-enhancing or juxtacortical lesions, were not associated with retinal layer thicknesses. Conclusion: The presence of SC or IT lesions in RIS may be associated with retinal neuro-axonal loss, supporting the presence of more disseminated disease.
机构:
Inha Univ, Sch Med, Dept Ophthalmol, Inchon, South Korea
Inha Univ, Sch Med, Inha Vis Sci Lab, Inchon, South KoreaInha Univ, Sch Med, Dept Ophthalmol, Inchon, South Korea
Lee, Kang Hoon
Kim, Chan Yun
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Yonsei Univ, Coll Med, Dept Ophthalmol, Inst Vis Res, Seoul, South KoreaInha Univ, Sch Med, Dept Ophthalmol, Inchon, South Korea
机构:
Univ Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USA
Okuda, D. T.
Mowry, E. M.
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Univ Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USA
Mowry, E. M.
Cree, B. A. C.
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Univ Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USA
Cree, B. A. C.
Crabtree, E. C.
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Univ Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USA
Crabtree, E. C.
Goodin, D. S.
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Univ Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USA
Goodin, D. S.
Waubant, E.
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Univ Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USA
Waubant, E.
Pelletier, D.
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Univ Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Neurol, UCSF Multiple Sclerosis Ctr, San Francisco, CA 94143 USA
机构:
Univ Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South KoreaUniv Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South Korea
Moon, Haein
Yoon, Joo Young
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Univ Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South KoreaUniv Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South Korea
Yoon, Joo Young
Lim, Hyun Taek
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Univ Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South KoreaUniv Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South Korea
Lim, Hyun Taek
Sung, Kyung Rim
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Univ Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South KoreaUniv Ulsan, Dept Ophthalmol, Coll Med, Asan Med Ctr, Seoul 138736, South Korea