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Cornea and Conjunctiva

Corneal Subbasal Nerve Plexus Evaluation by in Vivo Confocal Microscopy in Multiple Sclerosis: A Potential New Biomarker

ORCID Icon, , , , , , & show all
Pages 1452-1459
Received 15 Sep 2020
Accepted 26 Feb 2021
Accepted author version posted online: 18 Mar 2021
Published online: 06 Apr 2021
 

ABSTRACT

Purpose/Aim: Our study aims to evaluate corneal subbasal nerve plexus morphology by in vivo corneal confocal microscopy (CCM) in Multiple Sclerosis (MS) patients and to explore its potential ability to distinguish between MS patients and healthy subjects.

Materials and methods: Cross-sectional study, including 60 MS patients and 22 healthy subjects. Expanded Disability Status Scale (EDSS) was used to assess neurological disability. All participants underwent full ophthalmology evaluation, CCM and optical coherence tomography (OCT). Corneal nerve fibre density (CNFD), branch density (CNBD), fibre length (CNFL) and fibre tortuosity (CNFT) were analysed. Generalized additive regression models were used to analyse the data.

Results: Compared to controls, MS patients had lower CNFD, CNBD and CNFL (p < .001) and higher CNFT (p = .002). The area under the ROC curve to distinguish MS patients from healthy controls with CNFD and CNBD was 0.84 (95%CI: 0.75 to 0.93; 95%CI: 0.75 to 0.92, respectively). A nonlinear association between EDSS and CNFD was found, with an initial density increase followed by a significant decrease until more severe disability status. EDSS was associated with CNFL and CNBD, with values being significantly lower for patients with an EDSS > 2.5 (−2.06 mm/mm2; 95%CI: −3.84 to −0.28; p = .027 and −8.70 branches/mm2; 95%CI: −14.69 to −2.71; p = .006, respectively). An optic neuritis (ON) history did not influence CCM parameters.

Conclusions: Our results confirm CCM parameters’ potential to differentiate MS patients from healthy subjects, not being influenced by a previous ON history. A significant relationship between patient’s disability and corneal nerve morphology was also found.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Aknowledgements

Special thanks to Dr Carlos Capela, member of the Neurology Department of the Centro Hospitalar Universitário de Lisboa Central, for the substantial contribution he gave to our research.

Data availability statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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