| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Pignolet, Beatrice |
| dc.contributor.author | Rio Izquierdo, Jordi |
| dc.contributor.author | Vermersch, Patrick |
| dc.contributor.author | deSèze, Jerome |
| dc.contributor.author | Montalban, Xavier |
| dc.contributor.author | Comabella Lopez, Manuel |
| dc.contributor.author | Fissolo, Nicolás Miguel |
| dc.contributor.author | Ruet, Aurélie |
| dc.date.accessioned | 2022-04-04T13:01:51Z |
| dc.date.available | 2022-04-04T13:01:51Z |
| dc.date.issued | 2021-07 |
| dc.identifier.citation | Fissolo N, Pignolet B, Rio J, Vermersch P, Ruet A, deSèze J, et al. Serum Neurofilament Levels and PML Risk in Patients With Multiple Sclerosis Treated With Natalizumab. Neurol Neuroimmunol Neuroinflammation. 2021 Jul;8(4):e1003. |
| dc.identifier.issn | 2332-7812 |
| dc.identifier.uri | https://hdl.handle.net/11351/7293 |
| dc.description | Natalizumab; Serum Neurofilament |
| dc.description.abstract | Objectives The study aimed to assess the potential for serum neurofilament light chain (NFL) levels to predict the risk of progressive multifocal leukoencephalopathy (PML) in natalizumab (NTZ)-treated patients with multiple sclerosis (MS) and to discriminate PML from MS relapses.
Methods NFL levels were measured with single molecule array (Simoa) in 4 cohorts: (1) a prospective cohort of patients with MS who developed PML under NTZ therapy (pre-PML) and non-PML NTZ-treated patients (NTZ-ctr); (2) a cohort of patients whose blood was collected during PML; (3) an independent cohort of non-PML NTZ-treated patients with serum NFL determinations at 2 years (replication cohort); and (4) a cohort of patients whose blood was collected during exacerbations.
Results Serum NFL levels were significantly increased after 2 years of NTZ treatment in pre-PML patients compared with NTZ-ctr. The prognostic performance of serum NFL levels to predict PML development at 2 years was similar in the NTZ-ctr group and replication cohort. Serum NFL levels also distinguished PML from MS relapses and were 8-fold higher during PML compared with relapses.
Conclusions These results support the use of serum NFL levels in clinical practice to identify patients with relapsing-remitting MS at higher PML risk and to differentiate PML from clinical relapses in NTZ-treated patients.
Classification of Evidence This study provides Class I evidence that serum NFL levels can identify NTZ-treated patients with MS who will develop PML with a sensitivity of 67% and specificity of 80%. |
| dc.language.iso | eng |
| dc.publisher | Lippincott Williams & Wilkins |
| dc.relation.ispartofseries | Neurology-Neuroimmunology & Neuroinflammation;8(4) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Esclerosi múltiple - Tractament |
| dc.subject | Filaments citoplasmàtics |
| dc.subject | Avaluació de resultats (Assistència sanitària) |
| dc.subject.mesh | Multiple Sclerosis |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Neurofilament Proteins |
| dc.subject.mesh | /blood |
| dc.title | Serum Neurofilament Levels and PML Risk in Patients With Multiple Sclerosis Treated With Natalizumab |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1212/NXI.0000000000001003 |
| dc.subject.decs | esclerosis múltiple |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | proteínas de neurofilamentos |
| dc.subject.decs | /sangre |
| dc.relation.publishversion | https://doi.org/10.1212/NXI.0000000000001003 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Fissolo N, Comabella M] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Pignolet B] CRC-SEP Neurosciences Centre Hospitalier Universitaire Toulouse, CPTP INSERM UMR 1043 CNRS UMR 5282 et Université de Toulouse III, UPS, France. [Rio J, Montalban X] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Vermersch P] Univ. Lille, Inserm U1172, CHU Lille, FHU Imminent, France. [Ruet A] CHU de Bordeaux, INSERM-CHU CIC-P 0005, Service de Neurologie, Bordeaux F-33076, France. Université de Bordeaux, Bordeaux F-33076, France. [deSèze J] Department of Neurology, Hôpital Civil, Strasbourg |
| dc.identifier.pmid | 33903203 |
| dc.identifier.wos | 000711800300019 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |