The prevalence and characteristics of epilepsy in patients with relapsing-remitting multiple sclerosis treated with disease-modifying therapy
Authors:
J. Kolčava; J. Kočica; P. Štourač; J. Bednařík
Authors‘ workplace:
Medicine, Masaryk University and University Hospital, Brno, Czech Repubic
; Department of Neurology, Faculty of
Published in:
Cesk Slov Neurol N 2020; 83/116(4): 424-427
Category:
Short Communication
doi:
https://doi.org/10.14735/amcsnn2020424
Overview
Aim: The aim was to identify and describe patients with relapsing-remitting MS (RRMS) treated with a disease-modifying therapy who had a history of unprovoked seizure or epilepsy and to investigate the impact of epilepsy on the course and prognosis of MS.
Materials and methods: Patients with RRMS treated with a disease-modifying therapy at a large MS centre of the university hospital by January 1, 2019 were included in this study. The annual relapse rate and Expanded Disability Status Scale (EDSS) before and after the first seizure were evaluated.
Results: 17 patients (2.27%) with a history of unprovoked seizure or epilepsy were identified within the cohort of RRMS patients (N = 750). Active epilepsy, defined as the use of antiepileptic drugs or incidence of seizures within the last 5 years, was disclosed in 13 (73%) of them. Three patients had developed epilepsy before the first signs of MS. The mean annual relapse rates in patients with epilepsy before and after the first seizure were 0.12 and 0.5 (P = 0.1), resp. No significant difference was found in terms of EDSS worsening at 2 years before and after the first seizure (0.55 vs. 0.7; P = 0.38). The attack semiology and/or electroencephalogram recordings indicated a focal onset of seizures in 8 out of 17 patients (47%).
Conclusion: The frequency of unprovoked seizure or epilepsy among RRMS patients in our cohort was 2.27%.
Keywords:
Multiple sclerosis – Epilepsy – prevalence – seizures
Introduction
Multiple sclerosis is a chronic inflammatory and degenerative disease of the CNS. It is the leading cause of neurologic disability (not arising out of trauma) in young adults and is characterized by focal white matter lesions; however, both deep and cortical grey matter are also involved [1,2]. Patients with MS and epilepsy had a higher risk of mortality compared with those without [3]. A recent study derived from the Swedish MS registry (N = 14,545) revealed a cumulative incidence of epilepsy of 3.5% in patients with MS and 1.4% in controls. Patients with relapsing-remitting MS (RRMS) had a cumulative incidence of epilepsy of 2.2%, whereas in patients with the progressive disease this reached 5.5% [4].
The frequency of active epilepsy among MS patients in Nordland (county in Norway) was 3.2%, approximately 4.5 times higher than in the general Norwegian population. The RRMS patients with active epilepsy had more likely converted to secondary progressive MS than the patients without active epilepsy [5].
The cause of such an increased occurrence of epilepsy among patients with MS is unknown, but it is reasonable to assume an epileptogenic role played by cortical lesions [6,7]. The aim of our retrospective cohort study was to identify and describe patients with RRMS treated with a disease--modifying therapy who had a history of unprovoked seizure or epilepsy and to assess the impact of epilepsy on the course of MS in terms of the annual relapse rate (ARR) and Expanded Disability Status Scale (EDSS) at 2 years before and after the first seizure.
Materials and Methods
A cohort of 750 patients (504 women and 246 men) currently suffering from RRMS according to the McDonald diagnostic criteria, 2017 [8], seen at the MS centre of the large university hospital in the region of 612,000 inhabitants in the period leading up to January 1, 2019 were screened. Their case histories based on the electronic patient ledger were scrutinized to identify seizures. Epilepsy was classified as focal or generalized, based on recorded seizure semiology and EEG findings. The age, sex and treatment for MS and epilepsy were noted. The values of ARR and EDSS were analysed over the periods lasting for 2 years – both before and after the first seizure, to establish whether the seizures were directly involved in the severity of MS. The ANOVA (Analysis of Variance) test was used for the correlation of ARRs and EDSS in our cohort. Patients presenting with seizures before MS diagnosis were excluded from the ARR or EDSS analysis.
Results
Among 750 patients with RRMS treated with a disease-modifying therapy, 17 patients (age 41.2 ± 10.4 years) with a history of seizure (prevalence 2.27%) were identified, 12 of them were women (age 43.6 ± 10.5 years) and 5 men (35.6 ± 10.5 years). Three patients had epilepsy before the first symptoms of MS (18%) (Fig. 1). The mean ARRs in patients with epilepsy at 2 years before and after the first seizure were 0.12 and 0.5 (P = 0.1), resp. The mean values of EDSS at 2 years before and after the first seizure were 2.9 and 4.15, resp. The EDSS at the first seizure was 3.45 in the cohort (N = 10). No significant difference was found in terms of EDSS worsening at 2 years before and after the first seizure (0.55 vs. 0.7; P = 0.38).
Obr. 1. Latence od prvního symptomu RS k prvnímu záchvatu
The mean age at which the first symptoms of MS appeared was 27.6 ± 10.3 years and the mean age at which the first seizure occurred was 35.1 ± 12.6 years. At least one EEG was recorded for all patients with MS and epilepsy. Epileptiform discharges appeared in six patients (35%). The demographic and clinical data of the cohort were analysed (Tab. 1).
Eight out of 14 patients (57%) exhibited new T2-lesions on brain MRI findings after the first seizure. However, detailed analysis of MRI finding was not possible because of the retrospectivity of this study. The determination of the number or extent of cortical lesions was not possible due to a change in the MRI protocol over the follow-up and inability to detect reliable cortical lesions in older findings.
Discussion
The frequency of unprovoked seizure or epilepsy among RRMS patients in this cohort was 2.27%, which is higher than in the general population [9]. The frequency of focal epilepsy was 47%. There remains a possibility that patients with generalized seizure and normal EEG had a focal onset of seizure with a focal-to-bilateral tonic-clonic seizure; the frequency of focal epilepsy may, therefore, be underestimated. These findings are in agreement with international reports. There was found a non-significant trend towards an increase in ARR in patients with epilepsy at 2 years before and after the first seizure. No significant difference in the mean EDSS was found 2 years before and after the first seizure.
The accuracy of the diagnosis of epilepsy may, however, give cause for concern, especially among MS patients in whom there may be a range of paroxysmal symptoms such as muscle cramps, dystonia and other involuntary movements.
Furthermore, the high frequency of focal epilepsy disclosed supports the proposition that localized MS pathology lies behind comorbid epilepsy. MS patients with epilepsy have a higher prevalence of cortical lesions than patients without seizures in their case histories [6,10].
Coincidental occurrence of epilepsy and MS could account for some of the cases. It is also possible that several of these patients suffer from idiopathic epilepsy, clinically triggered in a nonspecific way by the cerebral metabolic disturbance resulting from about MS. It has been argued that acute symptomatic seizures are caused by new MS lesions and that chronic epilepsy is unrelated to new attacks of the disease, but rather to the epileptogenic effect of chronic cortical plaques. Cortical lesions are also an independent predictor of the conversion from a clinically isolated syndrome to MS [11].
Neuroinflammation plays an important role in the pathogenesis of MS but is also commonly activated in epileptogenic brain regions in humans and is clearly involved in animal models of epilepsy [12]. Thus, neuroinflammation could serve as a possible link from MS to epilepsy and explain the development of seizures in a subset of MS patients.
While MS lesions in the white matter are readily visualized by MRI, conventional MRI techniques are of low sensitivity in the detection of gray-matter MS pathology, a drawback that hinders accurate assessment of the total lesion burden. Newer MRI sequences such as double inversion recovery and phase-sensitive inversion recovery are 1.5–5 times more sensitive than conventional MRI sequences in the detection of cortical lesions [13].
The findings could have important implications for clinicians since there exists a need to be aware of the risk of epilepsy in people with MS. The clinician may, in particular, wish to consider whether the patient displays any other risk factors for epilepsy, such as medication and/or alcohol abuse, which might potentially exacerbate the risk. Because of the possibility of new seizures and status epilepticus, attention has been drawn to the importance of early use of antiepileptic drugs in MS patients with epilepsy. Clinicians should also be aware of the hypothetical proconvulsive properties of interferon-beta arising out of metabolic interference with antiepileptic drugs or caused by direct neurotoxic effects [14].
Some progression on MRI was found after the first seizure in 57% patients. However, detailed analysis of MRI findings was not possible because of the retrospectivity of the study. Due to a change in the MRI protocol over the follow-up, determination of the number or extent of cortical lesions was not possible. The retrospective study has its limits, but it is a good starting point for planning a prospective multicentre study.
Limitations
This is a single centre cohort retrospective study. It was not possible to use the ILAE classification 2017 accurately due to the retrospectivity of the study. No recent information about the accurate prevalence of epilepsy in our region was found. A small cohort of patients exhibits epilepsy in our study. Detailed analysis of MRI findings was not possible. It was not possible to compare patients with and without epilepsy in the framework of/connection with demographic data.
Ethics approval
The research was approved by the local ethics committees (FN Brno; 04-170419/EK; 17.4.2019).
Acknowledgment
Supported by the Ministry of Health of the Czech Republic. Grant ref.: MH CZ – DRO, FNBr, 65269705. Tony Long (Svinosice) helped work up the English.
Conflict of interest
The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study.
The Editorial Board declares that the manuscript met the ICMJE “uniform requirements” for biomedical papers.
Redakční rada potvrzuje, že rukopis práce splnil ICMJE kritéria pro publikace zasílané do biomedicínských časopisů.
Accepted for review: 8. 1. 2020
Accepted for print: 16. 6. 2020
MUDr. Jan Kočica
Department of Neurology Faculty of Medicine Masaryk University and University Hospital
Jihlavská 340/20
625 00 Brno
e-mail: kocica.jan@fnbrno.cz
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