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Routine CSF parameters as predictors of disease course in multiple sclerosis: An MSBase cohort study

  • Cathérine Dekeyser
  • , Matthias Hautekeete
  • , Melissa Cambron
  • , Vincent Van Pesch
  • , Francesco Patti
  • , Jens Kuhle
  • , Samia Khoury
  • , Jeanette Lechner Scott
  • , Oliver Gerlach
  • , Alessandra Lugaresi
  • , Davide Maimone
  • , Andrea Surcinelli
  • , Pierre Grammond
  • , Tomas Kalincik
  • , Mario Habek
  • , Barbara Willekens
  • , Richard Macdonell
  • , Patrice Lalive
  • , Tunde Csepany
  • , Helmut Butzkueven
  • Cavit Boz, Valentina Tomassini, Matteo Foschi, José Luis Sánchez-Menoyo, Ayse Altintas, Saloua Mrabet, Gerardo Iuliano, Maria Jose Sa, Raed Alroughani, Rana Karabudak, Eduardo Aguera-Morales, Orla Gray, Koen de Gans, Anneke van der Walt, Pamela A. McCombe, Norma Deri, Justin Garber, Abdullah Al-Asmi, Olga Skibina, Pierre Duquette, Elisabetta Cartechini, Daniele Spitaleri, Riadh Gouider, Aysun Soysal, Liesbeth Van Hijfte, Mark Slee, Maria Pia Amato, Katherine Buzzard, Guy Laureys
  • Ghent University
  • Sint-Jan Bruges Hospital
  • Université catholique de Louvain
  • University of Catania
  • Polyclinic Hospital University of Catania
  • University of Basel
  • Research Center for Clinical Neuroimmunology and Neuroscience (RC2NB)
  • American University of Beirut
  • University of Newcastle
  • Hunter New England Health
  • Zuyderland
  • Maastricht University
  • IRCCS Istituto delle Scienze Neurologiche di Bologna
  • University of Bologna
  • Azienda Ospedaliera Cannizzaro
  • Ospedale S. Maria delle Croci
  • CISSS Chaudière-Appalache
  • University of Melbourne, Peter MacCallum Cancer Centre
  • Royal Melbourne Hospital
  • University of Zagreb
  • University of Antwerp
  • Austin Health
  • University of Geneva
  • University of Debrecen
  • Monash University
  • Alfred Health
  • Karadeniz Technical University
  • Gabriele d'Annunzio University
  • University of L'Aquila
  • Galdakao-Usansolo University Hospital
  • Biocruces Health Research Institute
  • Koc University
  • Razi University Hospital
  • Université de Tunis El Manar
  • Ospedali Riuniti di Salerno
  • Centro Hospitalar Universitário de São João
  • University Fernando Pessoa
  • Al-Amiri Hospital
  • Yeditepe University
  • Koşuyolu University
  • Hospital Universitario Reina Sofía
  • Reina Sofía University Hospital-IMIBIC-UCO
  • South Eastern Health and Social Care Trust
  • Groene Hart Hospital
  • Royal Brisbane and Women's Hospital
  • University of Queensland
  • Hospital General de Agudos Juan Fernandez
  • Westmead Hospital
  • Sultan Qaboos University
  • The Alfred
  • Box Hill Hospital
  • University of Montreal
  • Azienda Sanitaria Unica Regionale Marche–AV3
  • Azienda Ospedaliera di Rilievo Nazionale e di Alta Specialità San Giuseppe Moscati
  • Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases
  • Flinders Medical Centre
  • University of Florence
  • IRCCS Fondazione Don Carlo Gnocchi - Milano

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5 Alıntılar (Scopus)

Özet

Background It remains unclear whether routine cerebrospinal fluid (CSF) parameters can serve as predictors of multiple sclerosis (MS) disease course. Methods This large-scale cohort study included persons with MS with CSF data documented in the MSBase registry. CSF parameters to predict time to reach confirmed Expanded Disability Status Scale (EDSS) scores 4, 6 and 7 and annualised relapse rate in the first 2 years after diagnosis (ARR2) were assessed using (cox) regression analysis. Results In total, 11 245 participants were included of which 93.7% (n=10 533) were persons with relapsing-remitting MS (RRMS). In RRMS, the presence of CSF oligoclonal bands (OCBs) was associated with shorter time to disability milestones EDSS 4 (adjusted HR=1.272 (95% CI, 1.089 to 1.485), p=0.002), EDSS 6 (HR=1.314 (95% CI, 1.062 to 1.626), p=0.012) and EDSS 7 (HR=1.686 (95% CI, 1.111 to 2.558), p=0.014). On the other hand, the presence of CSF pleocytosis (≥5 cells/ μL) increased time to moderate disability (EDSS 4) in RRMS (HR=0.774 (95% CI, 0.632 to 0.948), p=0.013). None of the CSF variables were associated with time to disability milestones in persons with primary progressive MS (PPMS). The presence of CSF pleocytosis increased ARR2 in RRMS (adjusted R2=0.036, p=0.015). Conclusions In RRMS, the presence of CSF OCBs predicts shorter time to disability milestones, whereas CSF pleocytosis could be protective. This could however not be found in PPMS. CSF pleocytosis is associated with short-term inflammatory disease activity in RRMS. CSF analysis provides prognostic information which could aid in clinical and therapeutic decision-making.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)1021-1031
Sayfa sayısı11
DergiJournal of Neurology, Neurosurgery and Psychiatry
Hacim95
Basın numarası11
DOI'lar
Yayın durumuYayınlandı - 2024
Harici olarak yayınlandıEvet

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