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Evaluation of Retinal Structure and Optic Nerve Function Changes in Multiple Sclerosis: Longitudinal Study with
Riwanti Estiasari1, Adisresti Diwyacitta1, Muhammad Sidik2
1Department of Neurology, Cipto Mangunkusumo General Hospital, Universitas Indonesia, Jakarta, Indonesia.
Neurology Research International
|July 5, 2021
Summary
Multiple sclerosis patients show worse retinal structure and optic nerve function compared to healthy individuals. Progressive thinning of retinal layers was observed over one year in MS patients.
Area of Science:
- Neuroscience
- Ophthalmology
- Immunology
Background:
- Multiple sclerosis (MS) is an autoimmune CNS disease causing inflammation and demyelination.
- The optic nerve is frequently affected, though optic neuritis (ON) occurs in only 20% of patients.
Purpose of the Study:
- Compare retinal structure and optic nerve function in MS patients versus healthy controls (HCs).
- Evaluate optic nerve alterations in MS over a 1-year follow-up.
- Analyze correlations between optic nerve changes and disease parameters (duration, relapses, disability, subtypes).
Main Methods:
- Prospective cohort study of 58 eyes from MS patients.
- Optic nerve function assessed via best-corrected visual acuity (BCVA), contrast sensitivity, and P100 latency.
- Retinal structure evaluated using ganglion cell-inner plexiform layer (GCIPL) and retinal nerve fiber layer (RNFL) thickness via OCT and fundus photography.
Main Results:
- MS patients exhibited lower BCVA, contrast sensitivity, GCIPL, and RNFL thickness than HCs (p<0.001).
- Significant GCIPL and RNFL (nasal) thinning occurred in MS patients at 6 and 12 months (p=0.007, p=0.004).
- Disease duration and relapses correlated with delayed P100 latency (r=-0.61, p<0.001; r=-0.46, p=0.02).
- SPMS subtype showed thinner GCIPL and RNFL than RRMS.
Conclusions:
- MS patients demonstrate poorer retinal structure and optic nerve function compared to controls.
- GCIPL and RNFL thinning progresses over 6-12 months.
- These structural changes did not correlate with disease duration, relapse count, or disability level in this study.

