TY - JOUR
T1 - Longitudinal analysis of retinal and choriocapillaris in patients with multiple sclerosis
T2 - a 3-year study
AU - Bostan, Mihai
AU - Li, Chi
AU - Cheong, Jia Wei
AU - Wong, Damon Wing Kee
AU - Tan, Bingyao
AU - Ismail, Munirah Binte
AU - Garhöfer, Gerhard
AU - Coroleuca, Ruxandra
AU - Schmetterer, Leopold
AU - Popa-Cherecheanu, Alina
AU - Chua, Jacqueline
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/3
Y1 - 2025/3
N2 - Objectives: This study investigated the longitudinal progression of retinal structure and microvasculature over 3 years in patients with relapsing–remitting multiple sclerosis (RRMS) using optical coherence tomography (OCT) and OCT angiography (OCTA). It also explored the correlation between these changes and the Expanded Disability Status Scale (EDSS) scores. Methods: In this prospective, longitudinal study, we enrolled 66 patients with RRMS without history of optic neuritis and 124 healthy controls. All participants underwent full ophthalmological examination, OCT/OCTA scans, and disability scoring (EDSS) at baseline and after 12 and 24 months. OCT data were analyzed for retinal layer thickness, while OCTA assessed microvascular perfusion in the retinal capillary plexuses and choriocapillaris. Statistical models evaluated yearly rates of change and their association with EDSS scores. Results: The patients with RRMS exhibited 3.6 times faster thinning of the inner plexiform layer (IPL; − 0.47 µm per year, P = 0.001) compared to controls over 3 years. Additionally, superficial retinal capillary layer perfusion density decreased more rapidly at − 0.44% per year (P = 0.006) in patients with MS. A strong correlation was found between worsening EDSS scores and accelerated ONL thinning (estimated coefficient: − 1.62 µm/per unit change of EDSS score, P = 0.004). Discussion: This study demonstrates progressive retinal neurodegeneration and microvascular dysfunction in patients with RRMS without a history of optic neuritis. The association between ONL thinning and increased disability supports the potential of OCT/OCTA as valuable tools for monitoring disease progression and severity in RRMS.
AB - Objectives: This study investigated the longitudinal progression of retinal structure and microvasculature over 3 years in patients with relapsing–remitting multiple sclerosis (RRMS) using optical coherence tomography (OCT) and OCT angiography (OCTA). It also explored the correlation between these changes and the Expanded Disability Status Scale (EDSS) scores. Methods: In this prospective, longitudinal study, we enrolled 66 patients with RRMS without history of optic neuritis and 124 healthy controls. All participants underwent full ophthalmological examination, OCT/OCTA scans, and disability scoring (EDSS) at baseline and after 12 and 24 months. OCT data were analyzed for retinal layer thickness, while OCTA assessed microvascular perfusion in the retinal capillary plexuses and choriocapillaris. Statistical models evaluated yearly rates of change and their association with EDSS scores. Results: The patients with RRMS exhibited 3.6 times faster thinning of the inner plexiform layer (IPL; − 0.47 µm per year, P = 0.001) compared to controls over 3 years. Additionally, superficial retinal capillary layer perfusion density decreased more rapidly at − 0.44% per year (P = 0.006) in patients with MS. A strong correlation was found between worsening EDSS scores and accelerated ONL thinning (estimated coefficient: − 1.62 µm/per unit change of EDSS score, P = 0.004). Discussion: This study demonstrates progressive retinal neurodegeneration and microvascular dysfunction in patients with RRMS without a history of optic neuritis. The association between ONL thinning and increased disability supports the potential of OCT/OCTA as valuable tools for monitoring disease progression and severity in RRMS.
KW - Expanded disability status scale
KW - Microvascular dysfunction
KW - Neurodegeneration
KW - Optical coherence tomography
KW - Optical coherence tomography angiography
KW - Relapsing–remitting multiple sclerosis
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U2 - 10.1007/s00415-025-12930-7
DO - 10.1007/s00415-025-12930-7
M3 - Article
AN - SCOPUS:85219638967
SN - 0340-5354
VL - 272
JO - Journal of Neurology
JF - Journal of Neurology
IS - 3
M1 - 237
ER -