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ITEM RESPONSE THEORY (IRT) METHODOLOGY CAN BE USED TO PLACE COMMON CLINICAL MEASURES OF MULTIPLE SCLEROSIS PROGRESSION ON A SINGLE LINEAR SCALE OF GENERAL NEUROLOGICAL DISABILITY [Meeting Abstract]

Chamot, Eric; Kister, Ilya; Cutter, Gary R.
ISI:000308138200036
ISSN: 1352-4585
CID: 178296

Increasing age at disability milestones among MS patients in the MSBase Registry

Kister, Ilya; Chamot, Eric; Cutter, Gary; Bacon, Tamar E; Jokubaitis, Vilija G; Hughes, Stella E; Gray, Orla M; Trojano, Maria; Izquierdo, Guillermo; Grand'maison, Francois; Duquette, Pierre; Lugaresi, Alessandra; Grammond, Pierre; Boz, Cavit; Hupperts, Raymond; Petersen, Thor; Giuliani, Giorgio; Oreja-Guevara, Celia; Iuliano, Gerardo; Lechner-Scott, Jeannette; Bergamaschi, Roberto; Rio, Maria Edite; Verheul, Freek; Fiol, Marcela; Van Pesch, Vincent; Slee, Mark; Butzkueven, Helmut; Herbert, Joseph
OBJECTIVE: To analyze time-trends in age at disability milestones among MS patients who were enrolled into the MSBase International Registry during 1996-2010 period. METHODS: We used linear regression to describe the relationship between mean age at major EDSS benchmarks and calendar time. We then assessed time-trend in age at initial EDSS rating with a three level linear growth model specifying that patients were nested within each of 20 participating countries. The model estimated the average of time-trends in mean age at initial clinical assessment within each country while controlling for patients' EDSS and sex in each country. Analyses were repeated in subsamples of patients diagnosed according to Poser or McDonald criteria. RESULTS: The MSBase Registry contained data on 11,108 MS patients enrolled between 1996 and 2010 who fulfilled our inclusion criteria. During the 1996-2010 period, enrollment age for patients with EDSS 4/4.5 increased by 7.9years, from 43 to 51years (p<0.001), and for EDSS 6/6.5 - by 4.9years, from 48 to 53year (p<0.001). These trends were consistent across 20 investigator countries and were observed in Poser-diagnosed as well as McDonald-diagnosed patient subsets. CONCLUSIONS: The more recent MSBase enrollees in each of the mild-to-moderate disability strata were significantly older than earlier enrollees. Possible explanations for this phenomenon are discussed.
PMID: 22507751
ISSN: 0022-510x
CID: 169245

Pencil-thin ependymal enhancement in neuromyelitis optica spectrum disorders

Banker, Piyush; Sonni, Smitha; Kister, Ilya; Loh, John P; Lui, Yvonne W
AQP4 water channels are thought to be the target of autoimmune attack in neuromyelitis optica-spectrum disorders (NMOsd). AQP4 are highly expressed on ventricular ependyma. The objective of this study was to describe a novel pattern of linear, 'pencil-thin' enhancement of ventricular ependyma in NMOsd. We report two NMOsd patients with pencil-thin ependymal enhancement along the frontal and occipital horns of lateral ventricles. Differential diagnosis of ependymal enhancement should include NMOsd alongside with infectious and neoplastic etiologies. Pencil-thin ependymal enhancement may be a helpful radiological marker of NMOsd that can be used to differentiate this condition from multiple sclerosis.
PMID: 22183933
ISSN: 1352-4585
CID: 172989

Conventional brain MRI in neuromyelitis optica

Cabrera-Gomez, J A; Kister, I
Background and purpose: Numerous case series have demonstrated that lesions on brain MRI are common in neuromyelitis optica (NMO), but there has not been an attempt to survey and synthesize the literature on neuro-radiology of brain findings in NMO. Objectives: To review the studies on conventional brain MRI in NMO and to propose to incorporate characteristic brain MRI lesions into the diagnostic criteria of NMO. Methods: We searched for articles with descriptions of brain MRI findings in NMO in EBSCO, EMBASE, PubMed/Medline, Science Citation Index, and SCOPUS. Results: Brain abnormalities are seen in majority of NMO patients as disease duration increases. A minority of NMO patients meet Barkhof criteria for space dissemination in multiple sclerosis (MS), and these criteria should not be used to exclude NMO diagnosis. Distinctive brain lesions of NMO are cataloged and described. Conclusions: Brain lesions in NMO are a consistent feature of the disease. International consensus MRI criteria are needed for NMO analogous to the existing criteria for MS.
PMID: 22040258
ISSN: 1351-5101
CID: 166812

Ultra-High-Field MR Imaging of Brain Lesions of Neuromyelitis Optica Spectrum Disorders (NMOsd): Absence of Central Venule within Lesions May Help Differentiate NMOsd from Multiple Sclerosis [Meeting Abstract]

Kister, Ilya; Herbert, Joseph; Ge, Yulin
ISI:000303204801511
ISSN: 0028-3878
CID: 166856

Natural History of MS Symptoms: Perceived Disease Impact across Disease Span in Nine Neurologic Domains among Enrollees in North American Research Committee on Multiple Sclerosis (NARCOMS) Registry [Meeting Abstract]

Kister, Ilya; Chamot, Eric; Salter, Amber; Cutter, Gary; Bacon, Tamar; Kalina, Jennifer; Herbert, Joseph
ISI:000303204804185
ISSN: 0028-3878
CID: 166857

Periependymal Abnormalities in Neuromyelitis Optica Spectrum Disorders and Multiple Sclerosis: A Case-Control Study [Meeting Abstract]

Raz, Eytan; Kister, Ilya; Omari, Mirza; Herbert, Joseph; Lui, Yvonne; Loh, John
ISI:000303204804208
ISSN: 0028-3878
CID: 166859

Differential Diagnosis of Adult-Onset Chronic Myelopathy: MRI-Based Approach [Meeting Abstract]

Zhovtis, Svetlana; Howard, Jonathan; Herbert, Joseph; Kister, Ilya
ISI:000303204801226
ISSN: 0028-3878
CID: 166865

The Kurtzke EDSS rank stability increases 4 years after the onset of multiple sclerosis: results from the MSBase Registry

Hughes, S; Spelman, T; Trojano, M; Lugaresi, A; Izquierdo, G; Grand'maison, F; Duquette, P; Girard, M; Grammond, P; Oreja-Guevara, C; Hupperts, R; Boz, C; Bergamaschi, R; Giuliani, G; Rio, ME; Lechner-Scott, J; van, Pesch V; Iuliano, G; Fiol, M; Verheul, F; Barnett, M; Slee, M; Herbert, J; Kister, I; Vella, N; Moore, F; Petkovska-Boskova, T; Shaygannejad, V; Jokubaitis, V; McDonnell, G; Hawkins, S; Kee, F; Gray, O; Butzkueven, H
Background The Expanded Disability Status Scale (EDSS) is widely used to rate multiple sclerosis (MS) disability, but lack of disease duration information limits utility in assessing severity. EDSS ranking at specific disease durations was used to devise the MS Severity Score, which is gaining popularity for predicting outcomes. As this requires validation in longitudinal cohorts, we aimed to assess the utility of EDSS ranking as a predictor of 5-year outcome in the MSBase Registry. Methods Rank stability of EDSS over time was examined in the MSBase Registry, a large multicentre MS cohort. Scores were ranked for 5-year intervals, and correlation of rank across intervals was assessed using Spearman's rank correlation. EDSS progression outcomes at 10 years were disaggregated by 5-year EDSS scores. Results Correlation coefficients for EDSS rank over 5-year intervals increased with MS duration: years 1-6=0.55, years 4-9=0.74, years 7-12=0.80 and years 10-15=0.83. EDSS progression risk at 10 years after onset was highly dependent on EDSS at 5 years; one-point progression risk was greater for EDSS score of >2 than
PMID: 22205675
ISSN: 0022-3050
CID: 158644

Increased risk of multiple sclerosis among women with migraine in the Nurses' Health Study II

Kister, Ilya; Munger, Kassandra L; Herbert, Joseph; Ascherio, Alberto
Background: The prospective Nurses' Health Study II (NHS-II), which enrolled over 116,000 female nurses, provides a unique opportunity to test the hypothesis of whether migraine is associated with multiple sclerosis (MS) and to explore the temporal aspects of the interrelationship. Objectives: To calculate relative risk of MS among NHS-II participants with and without migraine and to estimate odds ratio (OR) of being diagnosed with migraine in women with and without pre-existing MS. Methods: Cox proportional hazards regression was used to estimate rate ratios and 95% confidence intervals (CIs) of being diagnosed with MS in women with and without pre-existing migraine adjusted for potential confounders. Multivariate adjusted ORs of being diagnosed with migraine in women with and without pre-existing MS were estimated using logistic regression. Results: The prevalence of migraine in women with MS at baseline (26%, p = 0.11) and those diagnosed with MS after enrolment (29%, p < 0.0001) was higher than in the non-MS cases (21%). The relative risk of developing MS in migraineurs was 1.39 times higher than in non-migraineurs (95% CI 1.10-1.77, p = 0.008). The absolute risk of developing MS in women migraineurs over a 15-year follow-up was 0.47% and among non-migraineurs 0.32%. The odds of being diagnosed with migraine was higher in women with pre-existing MS compared with those without MS, but did not reach statistical significance (OR = 1.57, 95% CI 0.97-2.52; p = 0.06). Conclusions: Using a large, cohort of women-nurses, history of migraine was associated with an increased risk of MS. However, the difference in absolute risk of MS in migraineurs and non-migraineurs was small
PMCID:3627491
PMID: 21816759
ISSN: 1477-0970
CID: 149943