Volume 5 • Issue 2 • 1000220
J Mult Scler (Foster City), an open access journal
ISSN: 2376-0389
Drakulic et al., J Mult Scler (Foster City) 2018, 5:2
DOI: 10.4172/2376-0389.1000220
Research Article Open Access
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ISSN: 2376-0389
Journal of Multiple Sclerosis
*Corresponding author: Aleksic DZ, Department of neurology, Faculty of
Medical Sciences, University of Kragujevac, Serbia, Tel: 381642287184; E-mail:
drdeal1987@gmail.com
Received May 13, 2018; Accepted June 12, 2018; Published June 19, 2018
Citation: Drakulic SM, Vujic A, Arsic AA, Lazarevic S, Jevdjic J, et al. (2018) Event
Related Brain Potentials (ERP) Could Not Assess the Risk of Cognitive Impairment
in Relapse-Remitting Multiple Sclerosis (RRMS). J Mult Scler (Foster City) 5: 220.
doi: 10.4172/2376-0389.1000220
Copyright: © 2018 Drakulic SM, et al. This is an open-access article distributed
under the terms of the Creative Commons Attribution License, which permits
unrestricted use, distribution, and reproduction in any medium, provided the
original author and source are credited
Keywords: Event related brain potentials; Cognitive impairment;
Multiple sclerosis; PASAT; SDMT; INFβ
Introduction
Cognitive problems in patients with multiple sclerosis (MS) occur
widely in up to 62% of cases, especially concerning executive functions,
processing speed, attention, short-term memory and verbal fuency [1].
Te use of disease modifying therapies (DMTs), such as interferon
beta-1a (INFβ-1a) and interferon beta-1b (INFβ-1b) is considered
to afect the cognitive performance of patients with relapsing-
remitting multiple sclerosis (RRMS) [2-4], although there are opposite
opinions [5].
Cognitive assessment is performed using a battery of
neuropsychological tests, such as the Paced Auditory Serial Addition
Test 3 (PASAT-3) [6], and Symbol Digit Modalities Test (SDMT) [7-11].
In some studies with a small number of patients, p300 event-related
brain potentials (ERP) are considered to be an indicator of objective
neuropsychological cognitive functioning for measuring cognitive
function in patients with MS [12].
Te frst objective of our study was to determine whether there
are diferences between groups of patients receiving therapy, patients
without therapy and a control group, in terms of neuropsychological
test results and ERP. Te second objective was to determine factors that
may serve to assess the risk of cognitive impairment in patients with
RRMS.
Materials and Methods
Participants
In the period from 01.05.2016 to 01.07.2016 in the Department of
Neurology of the Clinical Center Kragujevac and the Faculty of medical
Sciences, University of Kragujevac, Kragujevac, Serbia, we examined a
total of 81 patients with RRMS (71.7%) and 32 healthy controls (28.3%).
We tested all patients from our center with RRMS who were on DMTs.
Te aims of our study were explained to them and informed consent
was signed by all participants and approved by the Ethics Committee of
the Clinical Center, Kragujevac.
Diagnosis of defnitive RRMS was made using the 2010 revisions to
the McDonald criteria [13]. All patients fulflled the inclusion criteria,
i.e. they had RRMS without disability in a functional system that would
prevent testing. Te exclusion criteria for the group of patients were
presence of other neurological diseases and psychiatric disorders, use
of neuroleptics, anticholinergics, antidepressants and antiepileptic
drugs, relapse and use of corticosteroid therapy in the last month before
the tests. Te inclusion criteria for the control group were absence
of: neurological disease, psychiatric diagnoses, use of any drugs. Te
RRMS group and the control group were matched by age, gender and
education.
Patients were divided into three subgroups: those who were not
receiving DMTs, patients on INF β-1a and patients on INFβ-1b. Some
patients were not receiving DMTs for economic (fnancial) reasons in
Serbia. Tey had not been given other types of DMTs earlier.
Event Related Brain Potentials (ERP) Could Not Assess the Risk of
Cognitive Impairment in Relapse-Remitting Multiple Sclerosis (RRMS)
Svetlana Miletic Drakulic
1
, Ana Vujic
2
, Ana Azanjac Arsic
1
, Snezana Lazarevic
1
, Jasna Jevdjic
3
, Dejan Z. Aleksic
1
*
1
Department of neurology, Faculty of Medical Sciences, University of Kragujevac, Serbia
2
Department of Pediatrics, Faculty of Medical Sciences, University of Kragujevac, Serbia
3
Department of Surgery, Faculty of Medical Sciences, University of Kragujevac, Serbia
Abstract
Objectives: The frst objective of our study was to determine differences between groups of patients receiving
disease modifying therapy (DMTs) (INFβ-1a and INFβ-1b), patients without DMTs and a control group, in terms of
neuropsychological tests and event-related brain potentials (ERP). The second objective was to determine factors that
may serve to assess the risk of cognitive impairment in patients with relapsing remitting multiple sclerosis (RRMS).
Methods: A total of 81 RRMS patients (mean age 41.09 ± 8.71 years old, 51 women, mean disease duration
133.05 ± 76.56 months) and 32 healthy controls participated in the study. Cognitive functions were evaluated using a
standard PASAT-3, the symbol digit modality test (SDMT) and ERP.
Results: There were statistically signifcant differences between the mean values for parietal (Pz) (p ≤ 0.05) and
central (Cz) latency (p<0.05) between the four groups of study participants. RRMS increased the risk of cognitive
impairment approximately 3.5 fold. Each year of age raised the risk of cognitive impairment by 6.0%. Each unit increase
in level of education reduced the risk of cognitive impairment approximately 2.5 fold. Increase in reaction time (RT) Cz
by 1 ms elevated the risk of cognitive impairment by 0.5%.
Conclusions: There were statistically signifcant differences between the mean values of Pz and Cz latency
between the four groups of study participants. Factors that may be used to assess the risk of developing cognitive
impairment in patients with RRMS include age, education level, and RT Cz. However, ERP (latency and amplitude) did
not independently assess the risk of cognitive impairment in RRMS patients.