Article Text

Research paper
Retinal nerve fibre layer thinning is associated with drug resistance in epilepsy
  1. Simona Balestrini1,2,
  2. Lisa M S Clayton1,
  3. Ana P Bartmann1,
  4. Krishna Chinthapalli1,
  5. Jan Novy1,
  6. Antonietta Coppola1,
  7. Britta Wandschneider1,
  8. William M Stern1,
  9. James Acheson3,
  10. Gail S Bell1,
  11. Josemir W Sander1,4,
  12. Sanjay M Sisodiya1
  1. 1Department of Clinical and Experimental Epilepsy, NIHR University College London Hospitals Biomedical Research Centre, UCL Institute of Neurology, London, UK
  2. 2Neuroscience Department, Polytechnic University of Marche, Ancona, Italy
  3. 3Department of Neuro-Ophthalmology, National Hospital for Neurology and Neurosurgery, London, UK
  4. 4Stichting Epilepsie Instellingen Nederland, Heemstede (SEIN), Heemstede, The Netherlands
  1. Correspondence to Professor Sanjay M Sisodiya; s.sisodiya{at}ucl.ac.uk

Abstract

Objective Retinal nerve fibre layer (RNFL) thickness is related to the axonal anterior visual pathway and is considered a marker of overall white matter ‘integrity’. We hypothesised that RNFL changes would occur in people with epilepsy, independently of vigabatrin exposure, and be related to clinical characteristics of epilepsy.

Methods Three hundred people with epilepsy attending specialist clinics and 90 healthy controls were included in this cross-sectional cohort study. RNFL imaging was performed using spectral-domain optical coherence tomography (OCT). Drug resistance was defined as failure of adequate trials of two antiepileptic drugs to achieve sustained seizure freedom.

Results The average RNFL thickness and the thickness of each of the 90° quadrants were significantly thinner in people with epilepsy than healthy controls (p<0.001, t test). In a multivariate logistic regression model, drug resistance was the only significant predictor of abnormal RNFL thinning (OR=2.09, 95% CI 1.09 to 4.01, p=0.03). Duration of epilepsy (coefficient −0.16, p=0.004) and presence of intellectual disability (coefficient −4.0, p=0.044) also showed a significant relationship with RNFL thinning in a multivariate linear regression model.

Conclusions Our results suggest that people with epilepsy with no previous exposure to vigabatrin have a significantly thinner RNFL than healthy participants. Drug resistance emerged as a significant independent predictor of RNFL borderline attenuation or abnormal thinning in a logistic regression model. As this is easily assessed by OCT, RNFL thickness might be used to better understand the mechanisms underlying drug resistance, and possibly severity. Longitudinal studies are needed to confirm our findings.

This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/

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