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White matter correlates of slowed information processing speed in unimpaired multiple sclerosis patients with young age onset
Govindarajan, Sindhuja Tirumalai; Liu, Yilin; Parra Corral, Maria Andrea; Bangiyev, Lev; Krupp, Lauren; Charvet, Leigh; Duong, Tim Q
Slowed information processing speed is among the earliest markers of cognitive impairment in multiple sclerosis (MS) and has been associated with white matter (WM) structural integrity. Localization of WM tracts associated with slowing, but not significant impairment, on specific cognitive tasks in pediatric and young age onset MS can facilitate early and effective therapeutic intervention. Diffusion tensor imaging data were collected on 25 MS patients and 24 controls who also underwent the Symbol Digit Modalities Test (SDMT) and the computer-based Cogstate simple and choice reaction time tests. Fractional anisotropy (FA), mean (MD), radial (RD) and axial (AD) diffusivities were correlated voxel-wise with processing speed measures. All DTI metrics of several white matter tracts were significantly different between groups (p < 0.05). Notably, higher MD, RD, and AD, but not FA, in the corpus callosum correlated with lower scores on both SDMT and simple reaction time. Additionally, all diffusivity metrics in the left corticospinal tract correlated negatively with SDMT scores, whereas only MD in the right superior fronto-occipital fasciculus correlated with simple reaction time. In conclusion, subtle slowing of processing speed is correlated with WM damage in the visual-motor processing pathways in patients with young age of MS onset.
PMID: 32748319
ISSN: 1931-7565
CID: 4553842
Upper Extremity Motor Fatigability as an Early Indicator in Pediatric Onset Multiple Sclerosis
Pilloni, Giuseppina; Malik, Martin; Malik, Raghav; Krupp, Lauren; Charvet, Leigh
AIM/UNASSIGNED:To adopt a computer-based protocol to assess grip fatigability in patients with pediatric-onset multiple sclerosis to provide detection of subtle motor involvement identifying those patients most at risk for future decline. METHOD/UNASSIGNED:Pediatric-onset multiple sclerosis patients were recruited during routine outpatient visits to complete a grip assessment and compared to a group of healthy age- and sex-matched controls. All participants completed a computer-based measurement of standard maximal grip strength and repetitive and sustained grip performance measured by dynamic and static fatigue indices. RESULTS/UNASSIGNED:< .001). CONCLUSION/UNASSIGNED:Brief repeatable grip assessment including measures of dynamic and sustained static output can be a sensitive indicator of upper extremity motor involvement in pediatric-onset multiple sclerosis, potentially identifying those in need of intervention to prevent future disability.
PMID: 33736529
ISSN: 1708-8283
CID: 4823522
Early neuropsychological markers of cognitive involvement in multiple sclerosis
Eilam-Stock, Tehila; Shaw, Michael T; Krupp, Lauren B; Charvet, Leigh E
BACKGROUND:Cognitive impairment due to multiple sclerosis (MS) is common and often limits occupational functioning, contributes to disability, and reduces quality of life. Early detection of cognitive involvement in MS is critical for treatment planning and intervention, and frequent, regular cognitive monitoring may provide insight into subtle changes in disease progression. OBJECTIVE:To compare the sensitivity and specificity of clinical, computer-based and experimental measures to early cognitive involvement in MS. METHODS:Cognitive functioning was compared in MS participants early in the disease course to matched healthy controls using conventional, computer-based and functional assessments: the Brief International Cognitive Assessment in MS (BICAMS); the computer-based Cogstate Brief Battery (CBB); the Attention Network Test-Interaction (ANT-I), including intra-individual variability; and the Test of Everyday Cognitive Ability (TECA), a functional measure of instrumental activities of daily living. RESULTS:MS participants (n = 25, mean disease duration= 5.82 ± 3.65 years) and demographically matched healthy controls (n = 29) completed the cognitive assessments. The Cogstate measure of choice reaction time (AUC = 0.73, p = .004), intra-individual variability on the ANT-I (AUC = 0.79, p = .001), and TECA (AUC = 0.78, p = .001) scores were the most sensitive and specific markers of cognitive involvement in MS. CONCLUSIONS:Brief, repeatable, computer-based measures of reaction time and variability detect early MS associated cognitive involvement.
PMID: 33639421
ISSN: 1878-5883
CID: 4800932
Gray Matter Morphometry Correlates with Attentional Efficiency in Young-Adult Multiple Sclerosis
Govindarajan, Sindhuja T; Pan, Ruiqi; Krupp, Lauren; Charvet, Leigh; Duong, Tim Q
Slowed processing on the alerting, orienting and executive control components of attention measured using the Attention Network Test-Interactions (ANT-I) have been widely reported in multiple sclerosis (MS). Despite the assumption that these components correspond to specific neuroanatomical networks in the brain, little is known about gray matter changes that occur in MS and their association with ANT-I performance. We investigated vertex-wise cortical thickness changes and deep gray matter volumetric changes in young MS participants (N = 21, age range: 18-35) with pediatric or young-adult onset and mild disease severity. ANT-I scores and cortical thickness were not significantly different between MS participants and healthy volunteers (N = 19, age range: 18-35), but thalamic volumes were significantly lower in MS. Slowed reaction times on the alerting component in MS correlated significantly with reduced volume of the right pallidum in MS. Slowed reaction times on executive control component correlated significantly with reduced thickness in the frontal, parietal and visual cortical areas and with reduced volume of the left putamen in MS. These findings demonstrate associations between gray matter changes and attentional performance even in the absence of widespread atrophy or slowed attentional processes.
PMCID:7826940
PMID: 33435314
ISSN: 2076-3425
CID: 4771442
Remote administration of the symbol digit modalities test to individuals with multiple sclerosis is reliable: A short report
Eilam-Stock, Tehila; Shaw, Michael T; Sherman, Kathleen; Krupp, Lauren B; Charvet, Leigh E
Background/UNASSIGNED:The Symbol Digit Modalities Test (SDMT) is the gold standard for cognitive screening in multiple sclerosis (MS). Objective/UNASSIGNED:Due to the recent COVID-19 pandemic and the increased need for virtual clinical visits, we examined the reliability of remote administration of the SDMT vs. standard in-person administration to individuals with MS. Methods/UNASSIGNED:Pearson's correlation analysis was performed between SDMT scores on the in-person and remote administrations. Results/UNASSIGNED: = .000). Conclusion/UNASSIGNED:Remote administration of the SDMT is a reliable cognitive screening approach in MS.
PMCID:7890734
PMID: 33643663
ISSN: 2055-2173
CID: 4801092
Characteristics and Predictors of Disease Course in Children Initially Presenting with ADEM [Meeting Abstract]
Rutatangwa, A; Aaen, G; Krysko, K M; Belman, A; Benson, L; Chitnis, T; Gorman, M; Goyal, M S; Graves, J; Harris, Y; Krupp, L; Lotze, T; Mar, S; Moodley, M; Ness, J; Rensel, M R; Rodriguez, M; Rose, J; Schreiner, T; Tillema, J; Weinstock-Guttman, B; Waltz, M; Casper, T; Waubant, E
Background: Acute disseminated encephalomyelitis (ADEM) is an inflammatory demyelinating central nervous system (CNS) disorder, characterized by new onset polyfocal neurologic symptoms with encephalopathy and multifocal demyelination, typically occurring in early childhood. The initial diagnosis of ADEM can be challenging as up to 20% of children with multiple sclerosis (MS) or neuromyelitis optica spectrum disorder (NMOSD) are initially diagnosed with ADEM.
Objective(s): To describe characteristics of patients with ADEM vs. recurrent demyelinating syndromes (MS or NMOSD) at the time of initial presentation and identify features at disease onset associated with monophasic demyelinating disease.
Method(s): This is a multicenter observational cohort study of children with a demyelinating disease diagnosis of ADEM, multiphasic ADEM, MS, and NMOSD who were followed at 12 regional pediatric MS referral centers in the US Network of Pediatric MS Centers. Descriptive statistics were used to report patient characteristics, clinical/imaging presenting features and clinical followup outcomes. Logistic regression was used to predict features associated with monophasic demyelination and to identify features associated with poor recovery from ADEM in patients with ADEM-like presentation at 2 years from disease onset.
Result(s): As of July 2019, 872 pediatric patients with a final diagnosis of ADEM (n=89), MS (n= 664) and NMOSD (n=119) were identified. The mean follow-up for all patients was 5.7 +/-3.1 years. ADEM patients were the youngest with mean age at first event 5.4 +/-3.7 years and male predominance (62%), p < 0.001. Severe clinical symptoms at onset were more frequent in ADEM (55% vs. 35% NMOSD and 15% MS, p < 0.001). After 2 years of follow-up, 86.2% of patients initially diagnosed with ADEM retained this diagnosis (ADEM to ADEM), while 10.1% were later reclassified as MS and 3.6% with NMOSD. In univariable regression, younger age at first event and having an antecedent infection at onset were associated with ADEM, while presentation with optic neuritis and gadolinium enhancement on brain MRI were associated with ADEM reclassification to MS or NMOSD after 2 years of follow up. In a multivariable analysis, older age at first event (OR 1.29 [95% CI 1.07-1.56], p = 0.007), presenting with optic neuritis (OR 27.56 [95% CI 3.19-238.14], p = 0.003) and presence of gadolinium enhancement on brain MRI at onset (OR 14.36 [95% CI 2.53-81.36], p = 0.003) were associated with reclassification of ADEM to MS or NMOSD within 2 years. Younger age at onset was associated with higher risk of EDSS 2.0 or higher after 2 years of follow-up (p = 0.0422).
Conclusion(s): Those who remain classified as ADEM vs. those who are reclassified as other demyelinating disorders are younger at onset, more likely to be male, have a more severe initial presentation, and are less likely to have optic neuritis or gadolinium enhancing lesions at onset
EMBASE:635559935
ISSN: 1477-0970
CID: 5088392
An Interview-Based Assessment of the Experience of Cognitive Impairment in Multiple Sclerosis: The Cognitive Assessment Interview (CAI)
Eilam-Stock, Tehila; Best, Pamela; Sherman, Kathleen; Shaw, Michael T; Ventura, Joseph; Krupp, Lauren B; Charvet, Leigh E
Background: Cognitive impairment is a common feature of multiple sclerosis (MS). A semi-structured interview, including informant input, can characterize the experience of individuals living with MS and cognitive involvement. Objective: We administered the Cognitive Assessment Interview (CAI), a patient- and informant-based semi-structured interview, to characterize the experience of cognitive impairments in those living with MS. Methods: Trained raters administered the CAI to a sample of MS participants and their informants enrolled for a trial of cognitive remediation. Cognitive impairments on the CAI were characterized and compared to those captured by neuropsychological and self-report measures. Results: A total of n = 109 MS participants (mean age = 50.3 ± 12.2) and their available informants (n = 71) were interviewed. Participants reported experiencing processing speed (90/106, 85%), working memory (87/109, 80%), and learning and memory (79/109, 72%) problems most commonly. CAI-based ratings were moderately correlated with a self-report measure (Multiple Sclerosis Neuropsychological Screening Questionnaire, rs = 0.52, p < 0.001) and only mildly correlated with objective neuropsychological measures specific to executive functions (r
PMCID:7905222
PMID: 33643211
ISSN: 1664-2295
CID: 4801072
Pediatric Onset-effects on Cognition and Long-term Learning [Meeting Abstract]
Krupp, L
Pediatric MS occurs in approximately 5% of patients and is defined as MS onset prior to age 18 years Those with pediatric MS tend to have a more inflammatory course but recover from relapses better than adults. Pediatric MS has been associated with cognitive problems in approximately 30% of patients where as 60-70% of adults have impaired cognitive functioning. Cognitive processing speed is the most frequently affected domain. In a recent study, 16% of CIS and 23% of RRMS had impaired cognitive functioning. Of concern is that other work has shown that while those with pediatric onset do well early in their course, over their life-time they may continue to show declines, particularly around 15 years after disease onset. The hope is that, early recognition, more effective symptomatic interventions such as cognitive retraining, and high efficacy disease modifying therapy can forestall the development of cognitive decline in those with pediatric MS onset
EMBASE:635559955
ISSN: 1477-0970
CID: 5148382
Mobile Attention Bias Modification Training Is a Digital Health Solution for Managing Distress in Multiple Sclerosis: A Pilot Study in Pediatric Onset
Charvet, Leigh; George, Allan; Cho, Hyein; Krupp, Lauren B; Dennis-Tiwary, Tracy A
PMCID:8355356
PMID: 34393986
ISSN: 1664-2295
CID: 5006312
Measuring the Symptoms and Impacts of Fatigue in Adults with Relapsing Multiple Sclerosis Using a Novel Disease Specific Scale: A Real-World Study in US Population [Meeting Abstract]
Azoulai, M; Levy-Heidmann, T; Morisseau, V; Jamieson, C; Charvet, L E; Krupp, L B; Lair, L L
Background: Fatigue is among the most frequent and disabling symptoms in RMS patients.
Objective(s): To measure multiple sclerosis (MS) fatigue and its impact on daily life in a real-world population using a survey including the relapsing MS (RMS)-specific Fatigue Symptoms and Impacts Questionnaire-Relapsing Multiple Sclerosis (FSIQ-RMS).
Method(s): This is an ongoing noninterventional prospective study of RMS patients recruited across the USA via an online survey. Participants completed questionnaires including disease history, disease status, sleep, social and emotional functioning, and the FSIQ-RMS, administered daily for 7 days. The FSIQ-RMS measures self-reported fatigue, and scores range from 0-100 (higher score = greater severity). The impact of fatigue on several aspects of patient's life was rated from 0 (no impact) to 10 (very high impact).
Result(s): A total of 300 RMS participants completed the 7-day assessment: mean age: 43.0 yrs; 88% women; mean diagnosis age: 32 yrs. Fatigue was reported as the symptom with the greatest impact on daily functioning. Participants with lower disability rated fatigue as the most impactful symptom on daily life. Fatigue was rated as severe, with a mean score: 57.3 for the FSIQ-RMS symptom domain; 3 impact sub-domain scores were 42.3, 43.4 and 50.1 (physical, cognitive/emotional, and coping). Fatigue severity did not vary among patients receiving high efficacy disease modifying therapy (DMT) vs other DMTs (44% [n=111] vs 56% [n=143], with score of 57.8?}17.6 vs 55.9?}19.8). Impact of ability to perform daily activities was rated as the highest (6.9/10) in terms of impact on patient's life. Because of MS, 44% of participants did not work. Among those who were working currently (48%), the impact of fatigue on professional life was rated as 4.5/10. Nearly half of the participants (49% of 300) discussed fatigue at each visit with their neurologists and 35% discussed at most visits, with 'impact of fatigue on quality of life' being the most discussed topic (65% of 289). Participants used different approaches to manage their fatigue including avoided heat exposure (77%), took breaks (65%), managed their energy (59%), took non-medicinal products (58%); however, only 6% (of 293) were totally satisfied with these strategies.
Conclusion(s): In this survey including the novel RMS specific FSIQ-RMS, fatigue occurred in most MS participants and adversely influenced patient's daily functioning and life. Fatigue remains a major concern for those with MS
EMBASE:635560083
ISSN: 1477-0970
CID: 5148362