Associations between neurofilament light chain levels, disease activity and brain atrophy in progressive multiple sclerosis
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
34092793
DOI
10.5507/bp.2021.034
Knihovny.cz E-zdroje
- Klíčová slova
- brain volume loss, multiple sclerosis, neurofilament light chain, no evident disease activity, progressive MS,
- MeSH
- atrofie MeSH
- biologické markery MeSH
- intermediární filamenta MeSH
- lidé MeSH
- magnetická rezonanční tomografie metody MeSH
- mozek diagnostické zobrazování patologie MeSH
- nemoci centrálního nervového systému * MeSH
- progrese nemoci MeSH
- relabující-remitující roztroušená skleróza * diagnostické zobrazování farmakoterapie patologie MeSH
- roztroušená skleróza * diagnostické zobrazování MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- biologické markery MeSH
BACKGROUND: Neurofilament light chain is a promising biomarker of disease activity and treatment response in relapsing-remitting multiple sclerosis (MS). Its role in progressive MS is less clear. AIM: The aim of the study was to assess the relationship between plasma neurofilament light chain (pNfL) and disease activity as defined by the concept NEDA-3 (No Evident Disease Activity), and brain volumetry, in a cohort of patients with the progressive disease form (PMS). METHODS: Levels of pNfL (SIMOA technology) were examined in 52 PMS patients and analysed in relationship to NEDA-3 status and annual brain volume loss (BVL) during the last 12 months. The statistical model was developed using logistic regression analysis, including demographic, clinical and magnetic resonance imaging (MRI) data as independent variables. Dependent variables were NEDA-3 status and BVL. RESULTS: The mean age of the study participants (n=52, 50% females) was 45.85 (SD, 9.82) and the median disability score was 5.0 (IQR: 5.0-5.5). ROC analysis showed that pNfL predicts NEDA-3 (the sensitivity and specificity of the model were 77.8% and 87.6%, respectively, P<0.001) and abnormal BVL (the sensitivity and specificity were 96.6% and 68.2%, respectively, P<0.001). CONCLUSIONS: The results show that pNfL levels are a useful biomarker of disease activity determined by NEDA-3 status, including brain MRI-volumetry, in patients with the progressive form of MS.
AXON Neuroscience R and D Services SE Bratislava Slovak Republic
Department of Neurology L Pasteur University Hospital Kosice Slovak Republic
Department of Neurology Pavol Jozef Safarik University in Kosice Slovak Republic
Institute of Neuroimmunology Slovak Academy of Sciences Bratislava Slovak Republic
Olomouc University Social Health Institute Palacky University Olomouc Czech Republic
Zobrazit více v PubMed
Kuhle J, Barro C, Disanto G, Mathias A, Soneson Ch, Bonnier G, Yaldizi O, Regeniter A, Derfuss T, Canales M, Schluep M, Du Pasquier R, Krueger G, Granziera C. Serum neurofilament light chain in early relapsing remitting MS is increased and correlates with CSF levels and with MRI measures of disease severity. Mult Scler 2016;22(12):1550-59. doi: 10.1177/1352458515623365 PubMed DOI
Håkansson I, Tisell A, Cassel P, Blennow K, Zettenberg H, Lundberg P, Dahle C, Vrethem M, Ernerudh J. Neurofilament levels, disease activity and brain volume during follow-up in multiple sclerosis. J Neuroinflammation 2018;15:209. doi: 10.1186/s12974-018-1249-7 PubMed DOI
Kuhle J, Kropshofer H, Haering DA, Kundu U, Meinert R, Barro C, Dahlke F, Tomic D, Leppert D, Kappos L. Blood neurofilament light chain as a biomarker of MS disease activity and treatment response. Neurology 2019;92(10):e1007-e1015. doi: 10.1212/WNL.0000000000007032 PubMed DOI
Siller N, Kuhle J, Muthuraman M, Barro Ch, Uphaus T, Groppa S, Kappos L, Zipp F, Bittner S. Serum neurofilament light chain is a biomarker of acute and chronic neuronal damage in early multiple scleosis. Mult Scler 2019;25(5):678-86. doi: 10.1177/1352458518765666 PubMed DOI
Novakova L, Zetterberg H, Sundström P, Axelsson M, Khademi M, Gunnarson M, Malmestrom C, Svenningsson A, Olsson T, Piehl F, Blennow K, Lycke J. Monitoring disease activity in multiple sclerosis using serum neurofilament light protein. Neurology 2017;89(22):2230-37. doi: 10.1212/WNL.0000000000004683 PubMed DOI
Disanto G, Barro C, Benkert P, Naegelin Y, Schadelin S, Giardiello A, Zecca C, Blennow K, Zettenberg H, Leppert D, Kappos L, Gobbi C, Kuhle J, Swiss multiple sclerosis cohort study group. Serum neurofilament light chain: a biomarker of neuronal damage in multiple sclerosis. Ann Neurol 2017;81(6):857-70. doi: 10.1002/ana.24954 PubMed DOI
Gionvannoni G, Tomic D, Bright JR, Havrdova E. "No evident disease activity": The use of combined assessments in the management of patients with multiple sclerosis. Mult Scler 2017;23(9):1179-187. doi: 10.1177/1352458517703193 PubMed DOI
Lublin FD, Reingold SC, Cohen JA, Cutter GR, Soelberg Sørensen P, Thompson AJ, Wolinsky JS, Balcer LJ, Banwell B, Barkhof F, Bebo B, Calabresi PA, Clanet M, Comi, G, Fox RJ, Freedman MS, Goodman AD, Inglese M, Kappos L, Kieseier BC, Lincoln JA, Lubetzki C, Miller AE, Montalban X, O'Connor PW, Petkau J, Pozzilli C, Rudick RA, Sormani MP, Stüve O, Waubant E, Polman CH. Defining the clinical course of multiple sclerosis. Neurology 2014;83:278-86. doi: 10.1212/WNL.0000000000000560 PubMed DOI
Radue EW, Barkhof F, Kappos L, Sprenger T, Haring DA, de Vera A, von Rosentiel P, Bright JR, Francis G, Cohen JA. Correlation between brain volume loss and clinical and MRI outcomes in multiple sclerosis. Neurology 2015;84(8):784-93. doi: 10.1212/WNL.0000000000001281 PubMed DOI
Sormani MP, Arnold DL, De Stefano N. Treatment effect on brain atrophy correlates with treatment effect on disability in multiple sclerosis. Ann Neurol 2014;75(1):43-49. doi: 10.1002/ana.24018 PubMed DOI
Sormani MP, Kappos L, Häring DA, Kropshofer H, Barro C, Leppert D, Tomic D, Kuhle J. Including blood neurofilament light chain in the NEDA concept in relapsing-remitting multiple sclerosis trials. Neurology (15 Supplement) S24.007 (2018) Corpus ID: 79895041 https://www.semanticscholar.org/paper
Weinstock-Guttman B, Medin J, Khan N, Korn JR, Lathi E, Silversteen J, Calkwood J, Silva D, Zivadinov R. MS-MRIUS Study Group. Assessing 'No Evidence of Disease Activity' status in patients with relapsing-remitting multiple sclerosis receiving fingolimod in routine clinical practice: a retrospective analysis of the multiple sclerosis clinical and magnetic resonance imaging outcomes in the USA (MS-MRIUS) Study. CNS Drugs 2018;(329313):1-10. doi: 10.1007/s40263-017-0482-4 PubMed DOI
Khalil M, Teunissen CE, Otto M, Piehl F, Sormani MP, Gattringer T, Barro C, Kappos L, Comabella M, Fazekas F, Petzold A, Blennow K, Zetterberg H, Kuhle J. Neurofilaments as biomarkers in neurological disorders. Nat Rev Neurol 2018;14(10):577-89. doi: 10.1038/s41582-018-0058-z PubMed DOI
De Stefano N, Stromillo ML, Giorgio A, Bartolozzi ML, Battaglini M, Baldini M, Portaccio E, Amato MP, Sormani MP. Establishing pathological cut-offs of brain atrophy rates in multiple sclerosis. J Neurol Neurosurg Psychiatry 2016;87(1):93-99. doi: 10.1136/jnnp-2014-309903 PubMed DOI
Uher T, Havrdova E, Sobisek L, Krasensky J, Vaneckova M, Seidl Z, Tyblova M, Ramasamy D, Zivadinov R, Horakova D. Is no evidence of disease activity an achieavable goal in MS patients on intramuscular interferon-beta-1a treatment over long-term follow-up? Mult Scler 2017;23(2):242-52. doi: 10.1177/1352458516650525 PubMed DOI
Kappos L, De Stefano N, Freedman MS, Cree BA, Radue EW, Sprenger T, Sormani MP, Smith T, Haring DA, Meier DP, Tomic D. Inclusion of brain volume loss in a revised measure of 'no evidence of disease activity' (NEDA-4) in relapsing-remitting multiple sclerosis. Mult Scler 2016;22(10):1297-305. doi: 10.1177/1352458515616701 PubMed DOI
Kurtzke RF. Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology 1983;33(11):1444-452. doi: 10.1212/wnl.33.11.1444 PubMed DOI
Kuhle J, Barro C, Andreasson U, Derfuss T, Lindberg R, sandelius A, Liman V, Norgren N, Blennow K, Zettenberg H. Comparison of three annalytical platforms for quantification of of the neurofilament light chain in blood samples: ELISA, electrochemiluminiscence immunoassay and Simoa. Clin Chem Lab Med 2016;54(10):1655-661. doi: 10.1515/cclm-2015-1195 PubMed DOI
Steenwijk MD, Amiri H, Schoonheim MM, de Sitter A, Barkhof F, Pouwels PJW, Vrenken H. Agreement of MSmetrix with established methods for measuring cross-sectional and longitudinal brain atrophy. Neuroimage Clin 2017;5:843-53. doi: 10.1016/j.nicl.2017.06.034 PubMed DOI
Koch MW, Cutter GR, Giovannoni G, Uitdehaag BMJ, Wolinsky JS, Steinerman JR, Knappertz V. Comparative study of disability progression measures in PPMS. Analysis of the PROMiSe data set. Neuro Neuroimmuno Neuroinflamm 2017;4(4):e358. doi: 10.1212/NXI.0000000000000358 PubMed DOI
European Medicines Agency Committee for medicinal products for human use. Guideline on clinical investigation of medical products for the treatment of multiple sclerosis EMA/CHPM/771815/2011, Rev.2, https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-clinical-investigation-medicinal-products-treatment-multiple-sclerosis (accessed 26 March 2015)
Kuhle J, Kropshofer H, Haring DA, Meinert R, Barro C, Dahlke F, Leppert D, Tomic D, Kappos L. Neurofilament light levels in the blood of patients with secondary progressive MS are higher than in primary progressive MS and may predict brain atrophy in both MS subtypes. Mult Scler J 2018;24:111.ECTRIMS Online Library.10/12/18; 232039; 286 https://onlinelibrary.ectrims-congress.eu/ectrims/2018/ectrims-2018/232039
Sellebjerg F, Börnsen L, Ammitzbøll C, Nielsen JE, Vinther-Jensen T, Hjermind LE, von Essen M, Ratzer RL, Sorensen PS, Christensen JR. Defining active progressive multiple sclerosis. Mult Scler 2017;23(13):1727-35. doi: 10.1177/1352458517726592 PubMed DOI
Bar-Or A, Cross AH, Bennett JL, von Budingen HC, Carruthers R, Edwards K, Eggers E, Fallis R, Fiore D, Gelfand JM, Giacomini P, Greenberg B, Hafler DA, Longbrake EE, Assman B, Ionete C, Kaunzner U, Lock C, Ma X, Musch B, Piehl F, Weber MS, Ziemssen T, Herman AE, Harp CT. Pretreatment cerebrospinal fluid (CSF) and serum neurofilament light (NfL) levels in patients with PPMS in the OBOE study are correlated and are higher in patients with PPMS with T1 Gd+ brain lesions. Mult Scler J 2019;25:494-95. ECTRIMS Online Library.09/12/19; 279308; P948. https://onlinelibrary.ectrims-congress.eu/ectrims/2019/stockholm/279308
Kapoor R, Sellebjerg F, Hartung HP, Arnold DL, Freedman MS, Jeffery D, Miller A, Edwards KR, Singh CM, Chang I, Ren Z, Sangurdekar D, Zhu B, Sheikh S, Mehta D, Ho PR, Campbell N, Edwards M, Fisher E, Kieseier BC, Rudick RA, Plavina T. Natalizumab reduced serum levels of neurofilament light chain in secondary progressive multiple sclerosis patients from the phase 3 ASCEND study. Mult Scler J 24(2 Suppl):988. doi: 10.1177/1352458518799980 DOI
Ferraro D, Guicciardi C, De Biasi S, Pinti M, Bedin R, Camera V, Vitetta F, Nasi M, Meletti S, Sola P. Plasma neurofilaments correlate with disability in progressive multiple sclerosis patients. Acta Neurol Scand 2020;141(1):16-21. doi: 10.1111/ane.13152 PubMed DOI
Barro C, Benkert P, Disanto G, Tsagkas C, Amann M, Naegelin Y, Leppert D, Gobbi C, Granziera C, Yaldizli Ö, Michalak Z, Wuerfel J, Kappos L, Parmar K, Kuhle J. Serum neurofilament as a predictor of disease worsening and brain and spinal cord atrophy in multiple sclerosis. Brain 2018;141:2382-91. doi: 10.1093/brain/awy154 PubMed DOI