alexa
Reach Us +1-947-333-4405
Detection of Cognitive Impairment in Multiple Sclerosis Based on P300 Event-Related Potential
ISSN: 2329-9096

International Journal of Physical Medicine & Rehabilitation
Open Access

Like us on:

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Detection of Cognitive Impairment in Multiple Sclerosis Based on P300 Event-Related Potential

Manuel Zwecker1,2*, Ida Sarova2,3, Mor Lavie2,3, Gabi Zeilig1,2 and Anat Achiron2,3
1Department of Neurological Rehabilitation, The Chaim Sheba Medical Center, Tel Hashomer, Israel
2Sackler Faculty of Medicine, Tel Aviv University, Israel
3Multiple Sclerosis Center, The Chaim Sheba Medical Center, Tel Hashomer, Israel
*Corresponding Author: Manuel Zwecker, Department of Neurological Rehabilitation, The Chaim Sheba Medical Center, Tel Hashomer 52621, Israel, Tel: +97235303725, Fax: +97235352888, Email: [email protected]

Received Date: Jul 19, 2018 / Accepted Date: Aug 01, 2018 / Published Date: Aug 03, 2018

Abstract

Objective: To investigate whether P300 event-related potential (ERP) is associated with cognitive impairments in early multiple sclerosis (MS).
Methods: 72 subjects with MS participated in this prospective case-control study. 56 (78%) had a disease duration of less than 3 years and 16 (12%) had significant, previously-established cognitive deficits. For all participants, P300 ERPs were examined using the odd-ball, paradigm and cognitive assessments were conducted using the Brief Repeatable Battery of Neuropsychological Tests (BRB-N) and the clock-drawing test (CDT).
Results: Of the 56 participants with early-stage MS, 61.5% had cognitive impairments, as defined by sub-normal scores on at least two cognitive subtests of the BRB-N or the CDT. Significant cognitive impairments were encountered in the following domains: verbal fluency (88.6%) assessed by the Word List Generation (WLG) test, short-term memory (70.5%) assessed by the Selective Reminding Test (SRT), visual-spatial learning (59.1%) assessed by the 10/36 Spatial Recall Test (10/36 SRT), CDT (45.5%), and sustained attention (29.5%) assessed by the Paced Auditory Serial Addition Test (PASAT). Significantly prolonged P300 latencies were recorded at Fz in the cognitive impairment group. None of the cognitive tests were found to be correlated with P300 latency at Fz in the early MS group. When participants with well-established cognitive impairments were included, P300 latency at Fz was correlated with WLG score, which assesses associative verbal fluency, a component of frontal lobe-associated executive functioning.
Conclusions: The present study showed that P300 latency at Fz might be useful in the detection of cognitive impairments in early stage MS. Moreover, in patients with MS who have severe cognitive impairments, P300 latency at Fz might detect impaired executive functions as assessed by the WLG test.

Keywords: Multiple sclerosis; Early MS; Cognitive impairment; P300 event-related potential (ERP); Executive functions; Frontal lobe; Word list generation (WLG)

Introduction

Cognitive dysfunction frequently occurs in individuals with multiple sclerosis (MS) and is considered a negative predictor of psycho-social functioning. Amato et al. [1] estimated that 45%-65% of MS patients have cognitive impairments. Other studies [2,3] have indicated that while cognitive impairments might have an early onset in the evolution of the disease, they might not be recognizable using common clinical tests. It is now evident that axonal injury caused by inflammation and neurodegenerative processes occurs in the earliest stages of MS. New techniques [4], such as the application of double inversion recovery (DIR) sequences in MRI examinations, have convincingly demonstrated that cortical lesions are frequent in patients with MS, even at the earliest clinical stages. Concurrently, it has been shown that patients who have cognitive deficits during the early stages of MS show more cortical lesions and more severe cortical atrophy than do cognitively preserved patients [5,6].

Cognitive domains such as attention, language, and memory may behave as interconnected neural networks that contain anatomically separate channels for transferring information [7]. Focal lesions or diffuse alteration of axons may interrupt these networks. The pathological characteristics of MS, a combination of multiple discrete lesions of the myelin and diffuse axonal pathology, are likely to explain the frequent occurrence of cognitive dysfunction associated with the disease. Various cognitive deficits, mainly affecting memory and attention, have been reported in up to 60% of patients with MS [8]. Although some previous studies suggest that cognitive impairments are more prevalent at later stages of the disease [9,10], some have detected such impairments at initial presentation [11] or during the early phase of the disease [12]. Achiron et al. [13] performed a study examining frequency and extent of cognitive deficits in patients with MS, revealing a 20.9% prevalence of cognitive impairments over a fiveyear period.

Electrophysiological recording of the P300 event-related potential (ERP) is often used in clinical practice [14] to determine cognitive involvement. Due to ease of recording and reliability, the P300 has become the most studied cerebral wave in the evaluation of cerebral information processing during the course of various neurological diseases. Particularly in psychiatric disorders and dementias [15], the P300 wave has proven to be clinically useful as an index of cognitive function [16]. Among the primary reasons for its popularity is the fact that it can be reliably elicited with relatively simple paradigms, without a behavioral response. P300 latency has been shown to be more sensitive to subtle changes in cognitive processing than reaction time measures. Changes in amplitude may reflect underlying structural and/or functional brain changes. As such, in combination with functional brain imaging, P300 may serve as an early indicator for dementia [15,17]. These recorded endogenous ERPs have also been specifically linked to cognitive and dementia-associated symptoms in MS [18].

The present study aimed to investigate whether the P300 ERP can be used to identify cognitive deficits during the early stage of MS. The hypothesis was that patients with early-stage MS would show discernible cognitive deficits associated with abnormal P300 ERPs.

Methods

Participants

The study group included 56 participants (mean age 33 ± 10.3 years, range 16-61 years, 37 females) with clinically definite recent onset MS, who were consecutively recruited at random from the outpatient clinic of the Neuro-Immunology and Multiple Sclerosis Center at Sheba Medical Center, Tel-Hashomer, Israel. Pre-assigned inclusion criteria were definite MS according to McDonald Criteria [19] and disease duration of less than three years. Participants with history of impaired hearing function, diagnosed psychiatric disorder, or cognitive impairment prior to MS diagnosis were excluded.

At a later stage, 16 additional participants with clinically definite MS and significant, previously-established cognitive impairments were recruited randomly and in succession from the same outpatient clinic. This group was included after a non-significant positive trend between the electrodiagnostic findings and cognitive impairment was found in early stage MS. It was assumed that including a study sample with increased overall cognitive difficulties would make the detection of a significant association more likely.

The study was approved by the Sheba Medical Center Ethics Committee. Written informed consent was obtained from all participants.

Procedure

All participants underwent ERP P300 examination and a neuropsychological assessment. The two procedures were performed with no more than three days between them.

P300 ERP

Recording conditions: ERPs were recorded in a silent electrodiagnostic laboratory. Electroencephalographic activity was recorded at Fz, Cz, and Pz electrode sites, according to the International 10-20 System, referenced to linked ears, with a forehead ground. Impedance was kept at 5 KΩ or less. Standard Ag/AgCl electrodes were used and affixed with electrode paste and glue after skin abrasion. An EOG electrode (Ag/AgCl) was placed to the left of the upper canthus of the right eye. Trials in which EOG activity exceeded +70 μV were automatically rejected. Bio-Logic Systems Corp. equipment was utilized with band-pass filter setting between 1 and 30 Hz and analysis time setting at 1024 msec with a 100 msec prestimulus base-line record.

Stimuli and procedures: P300 was elicited using an auditory “oddball” paradigm. Subjects were presented with two tones via headphones. The tone bursts varied in pitch and frequency of occurrence: one was a frequent or background tone presented at 1000 Hz, the other was infrequent and unpredictable (the “target” or the “oddball” tone) presented at 2000 Hz. The tones occurred at the rate of 1/sec, at a ratio of 1:4 at 50 dB above the patient’s hearing threshold, with a 10 msec rise/fall time and 40 msec duration. Subjects were instructed to keep a mental count of all “target” tones with their eyes closed. After a brief demonstration, two tests were performed, each continuing until 100 artifact-free infrequent stimuli responses were collected, and then averaged.

The electrodiagnostic examination was repeated at least twice in order to confirm reproducible wave form consistency.

P300 waveform analysis: P300 amplitude was determined as the highest positive post-stimulus deflection between 250 and 600 msec, measured from pre-stimulus baseline to peak. Latency values were obtained from the intersection of extrapolated lines from ascending and descending slopes of each peak.

Neuropsychological assessment

Cognitive status was assessed using one cognitive battery that is particularly relevant for and validated in MS, and widely used in both clinical practice and research: the Brief Repeatable Battery of Neuropsychological Tests (BRB-N) for MS [20] and the clock-drawing test (CDT) [21].

BRB-N: The BRB-N, which comprises five subtests, was administered and scored according to published procedures [22].

The Word List Generation (WLG) subtest measures associative verbal fluency. Participants were given 60 sec to say as many words as possible beginning with a particular letter. Overall number of words was counted and recorded.

The Selective Reminding Test (SRT) measures verbal learning and delayed recall through a multiple-trial list learning paradigm. Participants received a list of 12 words in the first trial. In each of five subsequent learning trials, only those items that were not recalled in the previous trial were selectively presented. After each trial the participant was instructed to recall all 12 words. Recall was also assessed after a delay of 11 minutes. Long-term storage scores were counted and used for assessment.

The Paced Auditory Serial Addition Task (PASAT) assesses sustained attention and concentration while a series of single digit numbers are aurally presented every 3 s. Participants were instructed to add each new number to the one presented immediately prior to it and report the result to the examiner. The percentage of correct responses was recorded.

The Symbol Digit Modality Test (SDMT) measures complex attention and concentration in a task that also requires speed and accuracy in visual search and scanning. Participants were asked to associate symbols with numbers and quickly generate the number when shown the symbol. The oral form of this test was used and the number of correct responses provided in 90 s was recorded.

The 10/36 Spatial Recall Test (10/36 SRT) assesses visual-spatial learning and delayed recall. Subjects viewed a 6 × 6 checkerboard with ten checkers on it for 10 s. They were then asked to reconstruct the pattern on a blank checkerboard. The total number of correct responses was recorded.

CDT: Each participant was given a sheet of paper with a pre-drawn circle on it and asked to draw the numbers on the clock and set the time to 10 past 11. Scoring was based on the method used by Shulman et al. [23]. Participants were defined as cognitively impaired if they performed below the normal range on at least two of the cognitive tasks, including the BRB-N subtests and the CDT.

Cognitive impairment definition: Participants were considered cognitively impaired if they had sub-normal scores on at least two cognitive subtests of the BRB-N or the CDT. The normal range was for each test was based on the relevant literature [24,25], and cut-off scores were as follows:

Word list generation: ≤ 14; Short-term memory ≤ 6; Late selective memory: ≤ 6; Paced auditory serial addition task: ≤ 80%; Symbol digit modalities test: ≤ 31; 10/36 Spatial recall test: ≤ 5 CDT: ≥ 2.

Demographic data: Demographic and disease-related data including age, gender, time since MS diagnosis, and level of disability were also collected. The Expanded Disability Status Scale (EDSS), which ranges from of 0 (normal) to 10 in increments of 0.5 [26] was used to quantify level of disability following a complete neurological examination.

Data Analysis

Demographic, clinical, neuropsychological, and electrophysiological data were analyzed using independent samples Student’s t-tests and the χ2 test (for gender distribution). Linear regression analyses were conducted to explore associations between electrophysiological and neuropsychological data. All tests were two-tailed, and p values of 0.05 or less were considered significant.

t-tests were used to compare the cognitive impairment and early MS groups with respect to P300 latencies and amplitudes at Fz, Pz and Cz.

Results

Demographic and disease-related data

Of the 56 patients with clinically definite MS and disease duration of three years, 84% were examined within the first year after diagnosis. Statistical analyses were performed on 52 patients due to missing data in the remaining 4 patients. Table 1 summarizes demographic and disease characteristics in early MS subjects with and without cognitive impairment.

Variable Early MS group (N=52)
No cognitive impairments Cognitive impairments
n=20 (38.5%) n=32 (61.5%)
Age (Mean ± SD) 39.8 ± 10.24 45.1 ± 10.37
Sex (%m/%f) 30/70 31.3/68.7
EDSS disability score (Mean ± SD) 2.0 ± 1.24 2.3 ± 1.24
WLG (% patholog.) 30% 84.4% p=0.000
SRT short-term memory (% patholog.) 20% 70.5% p=0.001
SRT long-term memory (% patholog.) 0% 6.3%
PASAT (% patholog.) 5% 25%
SDMT (% patholog.) 0% 6.3%
10/36 SRT (% patholog.) 20% 56.3% p=0.010
CDT (% patholog.) 0% 43.8% p=0.001

Table 1: Demographic data, disease characteristics, and cognitive task results in participants with short disease duration (Early MS) with and without cognitive impairments (WLG: Word List Generation; SRT: Serial Reminding Test; PASAT: Paced Auditory Serial Addition Task; SDMT: Symbol Digit Modality Test; 10/36 SRT: 10/36 Spatial Recall Test).

Variable Early MS (n=52) Cog. Imp. MS (n=16)
Age (Mean ± SD) 32.6 ± 10.3 41.1 ± 13.5, P=0.009
Sex (m%/f%) 66.1/33.9 56.3/43.8, n.s.
Disease duration 0.86 ± 0.90 9.81 ± 7.40, p=0.000
EDSS disability score 2.2 ± 1.22 5.41 ± 2.38, p=0.000
Word list generation 11.88 ± 4.41 8.31 ± 3.45, P=0.008
Short term memory 6.6 ± 1.83 5.23 ± 2.45, P=0.03
Late selective memory 10.0 ± 1.85 7.46 ± 2.63, p=0.000
PASAT 90 ± 19.8 73.46 ± 37.1, p=0.025
SDMT 46.2 ± 8.25 34.15 ± 9.96, p=0.000
10/36SRT 6.1 ± 2.23 4.15 ± 2.1, p=0.007
CDT 1.4 ± 0.73 1.92 ± 1.08, p=0.052

Table 2: Demographic data, disease characteristics, and cognitive task results in participants with short disease duration (Early MS) and established cognitive impairment (Cog. Imp. MS) regardless of disease duration (WLG: Word List Generation; SRT: Serial Reminding Test; PASAT: Paced Auditory Serial Addition Task; SDMT: Symbol Digit Modality Test; 10/36 SRT: 10/36 Spatial Recall Test).

ERP data

Table 3 summarizes the ERP results observed in participants with short disease durations.

Variable No cognitive impairments n=20 (38.5%) Cognitive impairments n=32 (61.5%) Severe cognitive impairment n=16
FzP300 Latency (msec) 309.3 ± 25.76 329.6 ± 34.25 p=0.035 372.8 ± 60.92
CzP300 Latency (msec) 317.3 ± 34.95 330.2 ± 32.72 384.2 ± 59.32
PzP300 Latency (msec) 321.8 ± 32.78 338.8 ± 36.99 390.0 ± 57.26
FzP300 Amplitude (µV) 7.47 ± 3.200 7.11 ± 4.081 4.42 ± 2.590
CzP300 Amplitude (µV) 10.33 ± 2.613 8.65 ± 3.778 6.52 ± 2.824
PzP300 Amplitude (µV) 11.61 ± 3.129 18.74 ± 54.526 8.15 ± 2.984

Table 3: Summary of event-related potential (ERP) results (Mean ± SD) observed in participants with short disease duration (Early MS) with and without cognitive impairments and the participants with severe cognitive impairment and long disease duration.

Regression analyses

To examine whether it was possible to predict P300 Fz latency during early-stage MS based on scores of the five cognitive subtests that were found to be significantly abnormal, a multiple linear regression analysis was conducted. The analysis yielded a nonsignificant regression equation, F(4,43)=1.059 ns.

Based on the results above, a group of participants with severe cognitive impairments were recruited with the aim of predicting P300 Fz latency based on a particular cognitive subtest of the two cognitive batteries. Following their inclusion, a second multiple linear regression was conducted to predict P300 Fz latency based on the five cognitive subtests in which participants with short disease duration and cognitive impairments showed significantly lower scores.

As shown in Table 2, the severe cognitive impairment group had a significantly higher number of abnormal scores on all the neuropsychological subtest categories, except for the short-term memory test.

The multiple regression analysis yielded a significant result, F(1,64)=9.24, p<0.003. Results showed that only WLG test scores, which reflect associative verbal fluency, predicted P300 latency at Fz. In accordance with this result, the mean P300 latency at Fz of participants who had scores within the normal range on the WLG test was 52.1 ms shorter than that of those who did not (Table 4).

ANOVA
  df SS MS F Significance F
Regression 1 16979.292 16979.3 9.242 0.003
Residual 64 117577.804 16979.3    
Total 65 134557.1      
  Coefficients Sig. Importance    
Intercept 381.166 0      
WLG -52.09 0.001 1    

Table 4: The results of the linear regression for FzP300 Latency.

Conclusion

P300 latency at the Fz site appears to provide a nonspecific, simple, and objective index of central nervous system dysfunction in early MS. The present research supports previous study results showing that cognitive impairments may be detectable at initial presentation [27], during the early phase, and in the presence of limited physical disability [38], and that they are more prevalent at later stages of the disease [13].

The identification of cognitive impairments in MS patients at early stages of the disease has important therapeutic and prognostic implications. Early diagnosis may improve patient management and, hopefully, the patient's quality of life. Further studies should be undertaken to validate the utility of P300 component latency at Fz as an indicator of the effectiveness of neuropsychological interventions, with an emphasis on cognitive rehabilitation. Future research may also clarify if P300 ERP examination restricted to recording latency at frontal lobe sites is sufficient for saving time and financial resources.

References

Citation: Zwecker M, Sarova I, Lavie M, Zeilig G, Achiron A (2018) Detection of Cognitive Impairment in Multiple Sclerosis Based on P300 Event-Related Potential. Int J Phys Med Rehabil 6: 479. doi:10.4172/2329-9096.1000479 DOI: 10.4172/2329-9096.1000479

Copyright: ©2018 Zwecker M, 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.  

Select your language of interest to view the total content in your interested language

Post Your Comment Citation
Share This Article
Relevant Topics
Article Usage
  • Total views: 360
  • [From(publication date): 0-0 - Mar 24, 2019]
  • Breakdown by view type
  • HTML page views: 336
  • PDF downloads: 24
Top