Searched for: person:kistei01
Anti-myelin oligodendrocyte glycoprotein (MOG) antibodies in patients with optic neuritis and seizures
Gutman, Josef Maxwell; Kupersmith, Mark; Galetta, Steven; Kister, Ilya
We describe four patients who experienced optic neuritis (ON) and seizures and were found to have antibodies to myelin oligodendrocyte glycoprotein (MOG) in serum. The index case was a previously healthy 39-year-old man who developed steroid dependent ON and had a generalized seizure when steroids were tapered. He tested positive for antibodies to MOG. We have reviewed the charts of all 11 anti-MOG antibody positive patients in our practice and found that 4 patients, all of whom had experienced one or more episodes of ON, also had a generalized seizure during the course of their illness. In 2 patients - including the index case - seizure occurred during steroid taper and in 2 others at the time of an episode of acute disseminated encephalomyelitis (ADEM). Association of anti-MOG antibodies and relapsing demyelinating disorders of the central nervous system is increasingly recognized. Testing for anti-MOG antibodies should be considered in patients with optic neuritis and seizures, especially in those with who also have a history of ADEM.
PMID: 29571858
ISSN: 1878-5883
CID: 3010732
Natalizumab Extended Interval Dosing Is Associated with a Reduction in Progressive Multifocal Leukoencephalopathy (PML) Risk in the Touch (R) Registry [Meeting Abstract]
Ryerson, Lana Zhovtis; Foley, John; Chang, Ih; Kister, Ilya; Cutter, Gary R.; Metzger, Ryan; Goldberg, Judith D.; Li, Xiaochun; Riddle, Evan; Yu, Bei; Ren, Zheng; Hotermans, Christophe; Ho, Pei-Ran; Campbell, Nolan
ISI:000429034600272
ISSN: 1352-4585
CID: 3039222
Exploratory PML risk assessment on Extended Interval Natalizumab Dosing. [Meeting Abstract]
Ryerson, Lana Zhovtis; Foley, John; Kister, Ilya; Frohman, Teresa; Pandey, Krupa; Lu, Xiaochun; Goldberg, Judith; Zuniga-Estrada, Guadalupe; Hoyt, Tammy; Jacob, April; Bacon, Tamar; Major, Eugene; Frohman, Elliot
ISI:000577381504074
ISSN: 0028-3878
CID: 5192172
Alternate dosing of fingolimod for Multiple Sclerosis [Meeting Abstract]
Kister, Ilya; Kantor, Daniel; Khoury, Samia; Rice, Marcus; Lathi, Ellen; Caminero Rodriguez, Ana Belen; Pawate, Siddharama; Bradshaw, Michael; Edwards, Keith; Cross, Anne; Parks, Becky; Lynch, Jennifer; Archer, Robert; Meador, William; Berkovich, Regina; Yamout, Bassem; Zeineddine, Maya; VanderKodde, Danita; Von Geldern, Gloria; Ge, Lily; Russell, Shira; Bacon, Tamar; Longbrake, Erin
ISI:000577381505274
ISSN: 0028-3878
CID: 5192192
Effect of Extended Interval Dose Natalizumab therapy on CD19+and CD34+cell mobilization from bone marrow and JC Viremia. [Meeting Abstract]
Ryerson, Lana Zhovtis; Monaco, Maria Chiara; Kister, Ilya; Zuniga-Estrada, Guadalupe; Jacob, April; Bacon, Tamar; Jensen, Peter; Major, Eugene
ISI:000577381504096
ISSN: 0028-3878
CID: 5192182
Predictors of relapses and disability progression after stopping disease-modifying therapies for multiple sclerosis [Meeting Abstract]
Kister, I; Spelman, T; Patti, F; Duquette, P; Trojano, M; Izquierdo, G; Lugaresi, A; Grammond, P; Sola, P; Ferraro, D; Grand'Maison, F; Alroughani, R; Terzi, M; Boz, C; Hupperts, R; Lechner-Scott, J; Kapos, L; Pucci, E; Hodgkinson, S; Solaro, C; Butzkueven, H
Background: MS patients often stop disease-modifying therapy (DMT). MSBase, a 50,000-patient, global observational MS registry, provides a unique opportunity to identify predictors of relapses and disease progression after DMTs are stopped. Objectives: To identify predictors of relapse and confirmed disability progression after stopping DMTs. Methods: We included MS patients who, at the time of stopping DMT, were >=18 years and were on a DMT continuously for >=1 year. We also required that, after stopping DMT, each patient be followed for >2 years; did not restart DMT for > 6 months (to exclude therapy 'switchers'); and did not become pregnant for >1 year. Predictors of time to first relapse and 3-month confirmed progression (1.5 EDSS steps for baseline EDSS 0; 0.5-for baseline EDSS 6-6.5; 1-for all others) were analyzed using Cox proportional hazards regression. Hazard proportionality was assessed with scaled Schoenfeld residuals; p< 0.05 was considered significant. Results: We identified 4,842 patients in the MSBase who met our inclusion criteria (74% female; mean (SD) age 40.7 years (10.4); mean (SD) disease duration 11.6 years (7.7)). Median (IQR) EDSS at baseline was 3 (1.5, 5.5). The discontinued DMTs were: IFNb-1a sc in 28%; IFNb-1b-26%; IFNb-1a im-20%; glatiramer acetate 18%; natalizumab-6%; fingolimod 3%. Most common reasons for discontinuation, recorded for 48% patients, were adverse events (9%), inconvenience (7%) and intolerance (7%). Post-DMT follow up was 31,691 patient-years. Post-DMT annualized relapse rate (ARR) was 0.22 and was lowest post-IFNb-1b (ARR=0.19) and highest post-Natalizumab (ARR=0.32). Disability data was available for 2,678 patients. The incidence of post-DMT confirmed disability progression was 8.23 per 100 person-years (95% CI: 7.72, 8.76); it was lowest post-IFNb-1a (6.40 (5.45, 7.51)) and highest post-Natalizumab (12.55 (10.04, 15.69). DMT was restarted by 2,984 (61.6%) patients after a median (IQR) of 18.22 months (IQR 10.97, 36.60). For each DMT, we will present predictors of time to relapse and confirmed disability progression, and DMT restart based on Cox regression model. Conclusions: Understanding risk factors for post-DMT relapses and disability accumulation after cessation of DMTs may allow clinicians to identify patients at low risk of disease worsening, who may choose to safely discontinue a particular DMT, and those at high risk, who would be well advised to continue on therapy
EMBASE:619357797
ISSN: 1477-0970
CID: 2871672
Clinical Reasoning: A patient with a history of encephalomyelitis and recurrent optic neuritis
Gutman, Josef Maxwell; Levy, Michael; Galetta, Steven; Kister, Ilya
PMCID:5679419
PMID: 29109139
ISSN: 1526-632x
CID: 2772062
Which symptoms contribute the most to patients' perception of health in multiple sclerosis?
Green, Rivka; Cutter, Gary; Friendly, Michael; Kister, Ilya
BACKGROUND: Multiple sclerosis is a polysymptomatic disease. Little is known about relative contributions of the different multiple sclerosis symptoms to self-perception of health. OBJECTIVES: To investigate the relationship between symptom severity in 11 domains affected by multiple sclerosis and self-rated health. METHODS: Multiple sclerosis patients in two multiple sclerosis centers assessed self-rated health with a validated instrument and symptom burden with symptoMScreen, a validated battery of Likert scales for 11 domains commonly affected by multiple sclerosis. Pearson correlations and multivariate linear regressions were used to investigate the relationship between symptoMScreen scores and self-rated health. RESULTS: Among 1865 multiple sclerosis outpatients (68% women, 78% with relapsing-remitting multiple sclerosis, mean age 46.38 +/- 12.47 years, disease duration 13.43 +/- 10.04 years), average self-rated health score was 2.30 ('moderate to good'). Symptom burden (composite symptoMScreen score) highly correlated with self-rated health (r = 0.68, P < 0.0001) as did each of the symptoMScreen domain subscores. In regression analysis, pain (t = 7.00), ambulation (t = 6.91), and fatigue (t = 5.85) contributed the highest amount of variance in self-rated health (P < 0.001). CONCLUSIONS: Pain contributed the most to multiple sclerosis outpatients' perception of health, followed by gait dysfunction and fatigue. These findings suggest that 'invisible disability' may be more important to patients' sense of wellbeing than physical disability, and challenge the notion that physical disability should be the primary outcome measure in multiple sclerosis.
PMCID:5588807
PMID: 28904811
ISSN: 2055-2173
CID: 2701412
Disease-modifying therapies can be safely discontinued in an individual with stable relapsing-remitting
Kister, Ilya
PMID: 28673111
ISSN: 1477-0970
CID: 2617192
Total hip and knee arthroplasty in multiple sclerosis patients: The NYU experience [Meeting Abstract]
Gutman, J; Schwarzkopf, R; Kister, I
Objective: To investigate indications for and outcomes of total hip and knee arthroplasty in patients with multiple sclerosis (MS). Background: MS patients may need joint replacement due to MS-related factors, such as falls or avascular necrosis, or for unrelated indications (eg primary/secondary osteoarthritis). Literature on outcomes of total joint replacement in MS patients is limited to case reports that highlight surgical complications or unusual presentations. There are no systematic reviews of indications for and short- and long-term outcomes of hip and knee arthroplasty in MS patients. Design/Methods: Retrospective chart review of NYU MS Center patients who underwent hip or knee arthroplasty after MS onset. Results: 13 MS patients followed at NYU MS Care Center underwent hip (N=8) or knee (N=5) replacement at NYU. Average age at surgery was 56+/-11 years (range 35-69 years) and MS duration was 16+/-9 years; 10/13 were female. 3 patients had prior joint trauma and 1 had avascular necrosis of the hip presumably from steroid use; the remainder suffered from osteoarthritis. Ambulatory status before surgery was: 4-walking unassisted, 7 - cane, 2 - bilateral assistance. Ambulatory status after surgery at last follow up was: 8 walking unassisted, 3 using a cane, and 2 using a walker. Perioperative complications included acute blood loss in 4, pneumonia in 2, DVT in 1, and urinary retention in 1. Reoperation was required in 1 patient for recurrent hip dislocation. Conclusions: Orthopaedic literature focuses on perioperative complications after total joint arthroplasty in MS patients, but our data on unselected patients show that the surgery appears to benefit most of them, though (mostly) non-neurologic complications were seen in approximately half of the cases. These data can help optimize selection and surgical management of MS patients who are considering knee or hip replacement. We intend to present additional data on our patients that will include patient-reported outcomes
EMBASE:616555869
ISSN: 1526-632x
CID: 2608492