Multiple Sclerosis and Related Disorders, Год журнала: 2021, Номер 52, С. 103006 - 103006
Опубликована: Май 7, 2021
Язык: Английский
Multiple Sclerosis and Related Disorders, Год журнала: 2021, Номер 52, С. 103006 - 103006
Опубликована: Май 7, 2021
Язык: Английский
Autoimmunity Reviews, Год журнала: 2020, Номер 19(5), С. 102512 - 102512
Опубликована: Март 12, 2020
Язык: Английский
Процитировано
139Journal of Neurology, Год журнала: 2019, Номер 267(12), С. 3489 - 3498
Опубликована: Май 25, 2019
Язык: Английский
Процитировано
123Annals of Neurology, Год журнала: 2020, Номер 88(3), С. 438 - 452
Опубликована: Июнь 7, 2020
The identification of progression in multiple sclerosis is typically retrospective. Given the profound burden progressive sclerosis, and recent development effective treatments for these patients, there a need to establish measures capable identifying early disease course. Starting from pathological findings, this review assesses state art potential able predict sclerosis. Future promising biomarkers that might shed light on mechanisms are also discussed. Finally, expansion concept by including an assessment cognition, patient-reported outcomes, comorbidities, considered. ANN NEUROL 2020;88:438-452.
Язык: Английский
Процитировано
87Multiple Sclerosis Journal, Год журнала: 2025, Номер unknown
Опубликована: Фев. 25, 2025
Background: Treatment with cladribine tablets (CladT) in relapsing–remitting multiple sclerosis (RRMS) reduced global grey matter (GM) atrophy, but the effects on regional GM are unknown. Objectives: This study aimed to investigate effect of CladT compared placebo magnetic resonance imaging (MRI)-derived patterns atrophy. Methods: We used MRI and clinical data from CLARITY study, including 393 people RRMS (CladT (3.5 mg/kg), n = 200 or placebo, 193) at baseline, 24, 48 96 weeks after treatment initiation. SynthSeg-derived volume changes atrophy derived source-based morphometry were analysed for group differences over time associations disability using mixed-effect models. Results: Deep (β −0.03, p < 0.01), thalamus −0.04, 0.01) brainstem–thalamus pattern 0.05) showed higher reduction treated group. These regions no during a predefined pseudo-atrophy period, where loss was worse Between W24 W96, Expanded Disability Status Scale (EDSS) scores associated lower deep −0.16, 0.001), thalamic −0.12, 0.05). Conclusion: clinically relevant slower neurodegeneration RRMS. Strongest seen GM, thalamus, brainstem, underlining importance measures assessing effects.
Язык: Английский
Процитировано
1Neurology, Год журнала: 2025, Номер 104(10)
Опубликована: Апрель 21, 2025
Sensitive and meaningful disability worsening measures remain an unmet medical need in multiple sclerosis (MS). Composite confirmed worsening/progression (cCDW/cCDP) combines the Expanded Disability Status Scale (EDSS) with performance tests of ambulation dexterity (Timed 25-Foot Walk Test [T25FWT] Nine-Hole Peg [9HPT]). We assessed relation changes these to understand utility cCDW/cCDP as endpoint for MS trials. Clinical trials measuring all components cCDW were selected analysis (i) individual patient-level data from Roche-sponsored studies characterize association between performance-test subsequent EDSS (ii) population-level published reporting treatment effects on either cCDP or T25FWT 9HPT events examine relationship events. Analysis (i): 6 Phase III comprising 4,979 patients relapsing-remitting (RRMS; n = 1,225), relapsing (RMS; 1,656), progressive (PMS; 922), primary (PPMS; 1,171), a cutoff November 2022, included patient analyses. For trials, associated increased risk (hazard ratios [HRs], p values: 2.11-5.20, 0.07-<0.001); similar associations found HRs later ranging 1.47 2.66 (p values 0.24-<0.001). without first 96 study weeks, weeks (HRs, 1.74-3.26, 0.01-<0.001; 1.45-3.08, 0.45-<0.001). Patients more likely experience ≥8-point change baseline at final visit 29-item Multiple Sclerosis Impact physical subscale (risk ratios, 1.45-2.17, 0.004-<0.001; 1.26-1.87, 0.15-0.03). (ii): In 9 included, predictive (Spearman correlation [95% CI] 0.82 [0.34-0.96], 0.005). this post hoc analysis, was harbinger correlated those EDSS. These results establish validity clinical relevance worsening, thus supporting use outcome progression ClinicalTrials.gov Identifiers: NCT01247324 (OPERA I); submitted 23, 2010; enrolled: August 31, 2011; available clinicaltrials.gov/study/NCT01247324. NCT01412333 II); 8, September 20, clinicaltrials.gov/study/NCT01412333. NCT03085810 (ENSEMBLE); March 16, 2017; 27, clinicaltrials.gov/study/NCT03085810. NCT01194570 (ORATORIO); 28, 3, clinicaltrials.gov/study/NCT01194570. NCT03523858 (CONSONANCE); April 2018; May clinicaltrials.gov/study/NCT03523858. NCT00087529 (OLYMPUS); July 9, 2004; clinicaltrials.gov/study/NCT00087529.
Язык: Английский
Процитировано
1Multiple Sclerosis Journal, Год журнала: 2020, Номер 27(9), С. 1421 - 1431
Опубликована: Ноя. 5, 2020
Background: Clinical measures in multiple sclerosis (MS) face limitations that may be overcome by utilising smartphone keyboard interactions acquired continuously and remotely during regular typing. Objective: The aim of this study was to determine the reliability validity keystroke dynamics assess clinical aspects MS. Methods: In total, 102 MS patients 24 controls were included observational study. Keyboard obtained with Neurokeys app. Eight timing-related features assessed for intraclass correlation coefficients (ICCs); construct analysing group differences (in fatigue, gadolinium-enhancing lesions on magnetic resonance imaging (MRI), vs controls); concurrent correlating disability measures. Results: Reliability moderate two (ICC = 0.601 0.742) good excellent remaining six 0.760–0.965). Patients had significantly higher latencies than controls. Latency between key presses correlated highest Expanded Disability Status Scale ( r 0.407) latency releases Nine-Hole Peg Test Symbol Digit Modalities (ρ 0.503 −0.553, respectively), ps < 0.001. Conclusion: Keystroke reliable, distinguished controls, associated Consequently, are a promising valid surrogate marker
Язык: Английский
Процитировано
43Cochrane library, Год журнала: 2022, Номер 2022(5)
Опубликована: Май 18, 2022
Язык: Английский
Процитировано
24Neuroradiology, Год журнала: 2019, Номер 61(2), С. 155 - 162
Опубликована: Янв. 8, 2019
Язык: Английский
Процитировано
43Journal of Neurology, Год журнала: 2019, Номер 267(4), С. 1035 - 1042
Опубликована: Дек. 17, 2019
Язык: Английский
Процитировано
40Multiple Sclerosis Journal, Год журнала: 2019, Номер 26(11), С. 1381 - 1391
Опубликована: Авг. 2, 2019
The objective of the study was to determine whether early infratentorial and/or spinal cord lesions are long-term cumulative predictors disability progression in multiple sclerosis (MS).We selected 153 MS patients from longitudinal Amsterdam cohort. Lesion analysis performed at baseline and year 2. Disability after 6 11 years measured using Expanded Status Scale (EDSS) EDSS-plus (including 25-foot walk 9-hole peg test). Patients with or were compared for risk 6- 11-year without lesions, respectively. Subsequently, on both locations only lesions.Baseline show a higher 6-year EDSS (odds ratio (OR): 3.6, p = 0.007) (OR: 2.5, 0.028) 2.8, 0.047). did not have than lesions.The presence seems be dominant factor progression. Simultaneous undisputedly predict
Язык: Английский
Процитировано
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