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Peer-reviewedCC BY 4.0Journal of Clinical Medicine

Longitudinal Retinal and Cervical Spinal Cord Changes in Multiple Sclerosis: Associations with Clinical, Cognitive, and Motor Measures

4 affiliations
  1. 1Department of Neurology, Faculty of Medicine, Bursa Uludağ University, 16059 Bursa, Türkiye
  2. 2Department of Ophthalmology, Faculty of Medicine, Bursa Uludağ University, 16059 Bursa, Türkiye
  3. 3Department of Radiology, Faculty of Medicine, Bursa Uludağ University, 16059 Bursa, Türkiye
  4. 4Department of Biostatistics, Faculty of Medicine, Bursa Uludağ University, 16059 Bursa, Türkiye

Abstract

Background/Objectives: Multiple sclerosis (MS) is a central nervous system disease that can cause severe disability. Identifying biomarkers associated with disease progression and disability is important for MS follow-up. Optical coherence tomography (OCT) parameters, measurements of cervical spinal atrophy, and cognitive and motor performance tests were evaluated along with their changes over one year to investigate their potential role in MS follow-up. Methods: This retrospective study included 79 patients with MS. OCT and cervical magnetic resonance imaging performed at 1-year intervals, along with cognitive and motor performance tests, were evaluated. Cervical mean cross-sectional area (mCSA) was used to assess spinal atrophy. Results: Over one year, cervical mCSA and ganglion cell–inner plexiform layer (GCIPL) measurements significantly decreased. Their annual changes were not significantly correlated in the Pearson analysis. The age-, sex-, and disease-duration-adjusted linear analysis likewise did not identify a statistically significant association. Conclusions: Cervical mCSA and GCIPL thickness significantly decreased over one year, but their changes were not significantly correlated. These findings suggest that cervical mCSA and GCIPL may provide complementary information on longitudinal structural changes in MS. However, because measurement reproducibility and absolute error were not quantified for the single-reader cervical measurements, the observed mCSA decrease should be interpreted cautiously, as the extent to which it reflects biological change rather than measurement variability remains uncertain. The clinical relevance of these findings requires further validation.

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BibTeX
@article{menguc2026longitudinal,
  title = {{Longitudinal Retinal and Cervical Spinal Cord Changes in Multiple Sclerosis: Associations with Clinical, Cognitive, and Motor Measures}},
  author = {Bedirhan Menguc and Emine Rabia Koc and Gamze Ucan Gunduz and Rifat Ozpar and Furkan Saridas and Guven Ozkaya},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = nov,
  doi = {10.3390/jcm15218491},
  url = {https://www.mdpi.com/2077-0383/15/21/8491},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Longitudinal Retinal and Cervical Spinal Cord Changes in Multiple Sclerosis: Associations with Clinical, Cognitive, and Motor Measures
AU  - Bedirhan Menguc
AU  - Emine Rabia Koc
AU  - Gamze Ucan Gunduz
AU  - Rifat Ozpar
AU  - Furkan Saridas
AU  - Guven Ozkaya
PY  - 2026
DA  - 2026/11/01
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15218491
UR  - https://www.mdpi.com/2077-0383/15/21/8491
AB  - Background/Objectives: Multiple sclerosis (MS) is a central nervous system disease that can cause severe disability. Identifying biomarkers associated with disease progression and disability is important for MS follow-up. Optical coherence tomography (OCT) parameters, measurements of cervical spinal atrophy, and cognitive and motor performance tests were evaluated along with their changes over one year to investigate their potential role in MS follow-up. Methods: This retrospective study included 79 patients with MS. OCT and cervical magnetic resonance imaging performed at 1-year intervals, along with cognitive and motor performance tests, were evaluated. Cervical mean cross-sectional area (mCSA) was used to assess spinal atrophy. Results: Over one year, cervical mCSA and ganglion cell–inner plexiform layer (GCIPL) measurements significantly decreased. Their annual changes were not significantly correlated in the Pearson analysis. The age-, sex-, and disease-duration-adjusted linear analysis likewise did not identify a statistically significant association. Conclusions: Cervical mCSA and GCIPL thickness significantly decreased over one year, but their changes were not significantly correlated. These findings suggest that cervical mCSA and GCIPL may provide complementary information on longitudinal structural changes in MS. However, because measurement reproducibility and absolute error were not quantified for the single-reader cervical measurements, the observed mCSA decrease should be interpreted cautiously, as the extent to which it reflects biological change rather than measurement variability remains uncertain. The clinical relevance of these findings requires further validation.
SN  - 2077-0383
ER  -