作者
Alyssa A Toorop,Mark HJ Wessels,Lynn Boonkamp,Liza M. Y. Gelissen,Elske Hoitsma,Esther Zeinstra,Luuk C van Rooij,Caspar E.P. van Munster,Anke Vennegoor,Jop Mostert,Beatrijs Wokke,Nynke F. Kalkers,E.L.J. Hoogervorst,Jeroen JJ van Eijk,Christiaan M Roosendaal,Jolijn J Kragt,M. Eurelings,Jessie van Genugten,Jessica Nielsen,LGF Sinnige,Mark E Kloosterziel,Edo P. J. Arnoldus,Gert W. van Dijk,Willem H. Bouvy,Eva Strijbis,Bob W. van Oosten,Brigit A. de Jong,Bernard M.J. Uitdehaag,Theo Rispens,Joep Killestein,Zoé L.E. van Kempen,Charlotte E. Teunissen
摘要
Background: Biomarkers of neuronal and axonal damage (serum neurofilament light (sNfL) and serum glial fibrillary acidic protein (sGFAP)) may provide insight into the aetiology of natalizumab wearing-off symptoms (WoSs). Objectives: We investigated the longitudinal association between and predictive value of sNfL and sGFAP and the occurrence of WoS in MS patients treated with natalizumab. Methods: We performed longitudinal measurements of sNfL and sGFAP in NEXT-MS trial participants who completed a questionnaire about WoS. Results: A total of 364 participants were included. In total, 55.5% presented with WoS and 44.5% without WoS during natalizumab treatment. Longitudinal analyses showed no association between sNfL and sGFAP levels and WoS at any timepoint. Biomarker levels at baseline did not predict first-time WoS occurrence. Conclusion: Acute and chronic neuronal and axonal damage are most likely not the underlying cause of WoS.