TY - JOUR
T1 - Risk of relapse phenotype recurrence in multiple sclerosis
AU - Kalincik, Tomas
AU - Buzzard, Katherine
AU - Jokubaitis, Vilija G
AU - Trojano, Maria
AU - Duquette, Pierre Pascal
AU - Izquierdo, Guillermo
AU - Girard, Marc
AU - Lugaresi, Alessandra
AU - Grammond, Pierre
AU - Grand'Maison, Francois
AU - Oreja-Guevara, Celia
AU - Boz, Cavit
AU - Hupperts, Raymond
AU - Petersen, Thor
AU - Giuliani, Giorgio
AU - Iuliano, Gerardo
AU - Lechner-Scott, Jeannette
AU - Barnett, Michael
AU - Bergamaschi, Roberto
AU - Van Pesch, Vincent
AU - Amato, Maria Pia
AU - Van Munster, Erik
AU - Fernandez-Bolanos, Ricardo
AU - Verheul, Freek
AU - Fiol, Marcela
AU - Cristiano, Edgardo
AU - Slee, Mark
AU - Rio, Maria Edite
AU - Spitaleri, Daniele La
AU - Alroughani, Raed A
AU - Gray, Orla M
AU - Saladino, Maria Laura
AU - Flechter, Sholmo
AU - Herbert, Joseph
AU - Cabrera-Gomez, Jose Antonio
AU - Vella, Norbert
AU - Paine, Mark
AU - Shaw, Cameron
AU - Moore, Fraser G A
AU - Vucic, Steve
AU - Savino, Aldo A
AU - Singhal, Bhim
AU - Petkovska-Boskova, Tatjana
AU - Parratt, John
AU - Sirbu, Carmen-Adella
AU - Rozsa, Csilla
AU - Liew, Danny
AU - Butzkueven, Helmut
AU - the MSBase Study Group
PY - 2014/10/19
Y1 - 2014/10/19
N2 - Objectives: The aim was to analyse risk of relapse phenotype recurrence in multiple sclerosis and to characterise the effect of demographic and clinical features on this phenotype. Methods: Information about relapses was collected using MSBase, an international observational registry. Associations between relapse phenotypes and history of similar relapses or patient characteristics were tested with multivariable logistic regression models. Tendency of relapse phenotypes to recur sequentially was assessed with principal component analysis. Results: Among 14,969 eligible patients (89,949 patient-years), 49,279 phenotypically characterised relapses were recorded. Visual and brainstem relapses occurred more frequently in early disease and in younger patients. Sensory relapses were more frequent in early or non-progressive disease. Pyramidal, sphincter and cerebellar relapses were more common in older patients and in progressive disease. Women presented more often with sensory or visual symptoms. Men were more prone to pyramidal, brainstem and cerebellar relapses. Importantly, relapse phenotype was predicted by the phenotypes of previous relapses. (OR = 1.8-5, p = 10-14). Sensory, visual and brainstem relapses showed better recovery than other relapse phenotypes. Relapse severity increased and the ability to recover decreased with age or more advanced disease. Conclusion: Relapse phenotype was associated with demographic and clinical characteristics, with phenotypic recurrence significantly more common than expected by chance.
AB - Objectives: The aim was to analyse risk of relapse phenotype recurrence in multiple sclerosis and to characterise the effect of demographic and clinical features on this phenotype. Methods: Information about relapses was collected using MSBase, an international observational registry. Associations between relapse phenotypes and history of similar relapses or patient characteristics were tested with multivariable logistic regression models. Tendency of relapse phenotypes to recur sequentially was assessed with principal component analysis. Results: Among 14,969 eligible patients (89,949 patient-years), 49,279 phenotypically characterised relapses were recorded. Visual and brainstem relapses occurred more frequently in early disease and in younger patients. Sensory relapses were more frequent in early or non-progressive disease. Pyramidal, sphincter and cerebellar relapses were more common in older patients and in progressive disease. Women presented more often with sensory or visual symptoms. Men were more prone to pyramidal, brainstem and cerebellar relapses. Importantly, relapse phenotype was predicted by the phenotypes of previous relapses. (OR = 1.8-5, p = 10-14). Sensory, visual and brainstem relapses showed better recovery than other relapse phenotypes. Relapse severity increased and the ability to recover decreased with age or more advanced disease. Conclusion: Relapse phenotype was associated with demographic and clinical characteristics, with phenotypic recurrence significantly more common than expected by chance.
KW - MSBase
KW - Multiple sclerosis
KW - phenotype
KW - presentation of neurological diseases
KW - prognosis
UR - https://www.scopus.com/pages/publications/84921019317
U2 - 10.1177/1352458514528762
DO - 10.1177/1352458514528762
M3 - Article
C2 - 24777276
AN - SCOPUS:84921019317
SN - 1352-4585
VL - 20
SP - 1511
EP - 1522
JO - Multiple Sclerosis Journal
JF - Multiple Sclerosis Journal
IS - 11
ER -