TY - JOUR
T1 - Optical coherence tomography versus other biomarkers
T2 - Associations with physical and cognitive disability in multiple sclerosis
AU - Cerdá-Fuertes, Nuria
AU - Stoessel, Marc
AU - Mickeliunas, Gintaras
AU - Pless, Silvan
AU - Cagol, Alessandro
AU - Barakovic, Muhamed
AU - Maceski, Aleksandra Maleska
AU - Álvarez González, Cesar
AU - D’ Souza, Marcus
AU - Schaedlin, Sabine
AU - Benkert, Pascal
AU - Calabrese, Pasquale
AU - Gugleta, Konstantin
AU - Derfuss, Tobias
AU - Sprenger, Till
AU - Granziera, Cristina
AU - Naegelin, Yvonne
AU - Kappos, Ludwig
AU - Kuhle, Jens
AU - Papadopoulou, Athina
N1 - Publisher Copyright:
© The Author(s), 2023.
PY - 2023/11
Y1 - 2023/11
N2 - Background: Optical coherence tomography (OCT) is a biomarker of neuroaxonal loss in multiple sclerosis (MS). Objective: The objective was to assess the relative role of OCT, next to magnetic resonance imaging (MRI) and serum markers of disability in MS. Methods: A total of 100 patients and 52 controls underwent OCT to determine peripapillary retinal nerve fiber layer (pRNFL) and ganglion cell-inner plexiform layers (GCIPL). Serum neurofilament light chain (sNfL), total lesion volume (TLV), and brain parenchymal fraction (BPF) were also assessed. The associations of OCT with disability were examined in linear regression models with correction for age, vision, and education. Results: In patients, pRNFL was associated with the Symbol Digit Modalities Test (SDMT; p = 0.030). In the multivariate analysis including sNfL and MRI measures, pRNFL (β = 0.19, p = 0.044) and TLV (β = −0.24, p = 0.023) were the only markers associated with the SDMT. pRNFL (p < 0.001) and GCIPL (p < 0.001) showed associations with the Expanded Disability Status Scale (EDSS). In the multivariate analysis, GCIPL showed the strongest association with the EDSS (β = −0.32, p < 0.001) followed by sNfL (β = 0.18, p = 0.024). Conclusion: The associations of OCT measures with cognitive and physical disability were independent of serum and brain MRI markers of neuroaxonal loss. OCT can be an important tool for stratification in MS, while longitudinal studies using combinations of biomarkers are warranted.
AB - Background: Optical coherence tomography (OCT) is a biomarker of neuroaxonal loss in multiple sclerosis (MS). Objective: The objective was to assess the relative role of OCT, next to magnetic resonance imaging (MRI) and serum markers of disability in MS. Methods: A total of 100 patients and 52 controls underwent OCT to determine peripapillary retinal nerve fiber layer (pRNFL) and ganglion cell-inner plexiform layers (GCIPL). Serum neurofilament light chain (sNfL), total lesion volume (TLV), and brain parenchymal fraction (BPF) were also assessed. The associations of OCT with disability were examined in linear regression models with correction for age, vision, and education. Results: In patients, pRNFL was associated with the Symbol Digit Modalities Test (SDMT; p = 0.030). In the multivariate analysis including sNfL and MRI measures, pRNFL (β = 0.19, p = 0.044) and TLV (β = −0.24, p = 0.023) were the only markers associated with the SDMT. pRNFL (p < 0.001) and GCIPL (p < 0.001) showed associations with the Expanded Disability Status Scale (EDSS). In the multivariate analysis, GCIPL showed the strongest association with the EDSS (β = −0.32, p < 0.001) followed by sNfL (β = 0.18, p = 0.024). Conclusion: The associations of OCT measures with cognitive and physical disability were independent of serum and brain MRI markers of neuroaxonal loss. OCT can be an important tool for stratification in MS, while longitudinal studies using combinations of biomarkers are warranted.
KW - EDSS
KW - GCIPL
KW - OCT
KW - RNFL
KW - SDMT
UR - http://www.scopus.com/inward/record.url?scp=85173475540&partnerID=8YFLogxK
U2 - 10.1177/13524585231198760
DO - 10.1177/13524585231198760
M3 - Article
C2 - 37772490
AN - SCOPUS:85173475540
SN - 1352-4585
VL - 29
SP - 1540
EP - 1550
JO - Multiple Sclerosis Journal
JF - Multiple Sclerosis Journal
IS - 13
ER -