NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis

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Standard

NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis. / Ammitzbøll, C.; Dyrby, T. B.; Börnsen, L.; Schreiber, K.; Ratzer, R.; Romme Christensen, J.; Iversen, P.; Magyari, M.; Lundell, H.; Jensen, P. E.H.; Sørensen, P. S.; Siebner, H. R.; Sellebjerg, F.

I: Multiple Sclerosis and Related Disorders, Bind 77, 104854, 2023.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Ammitzbøll, C, Dyrby, TB, Börnsen, L, Schreiber, K, Ratzer, R, Romme Christensen, J, Iversen, P, Magyari, M, Lundell, H, Jensen, PEH, Sørensen, PS, Siebner, HR & Sellebjerg, F 2023, 'NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis', Multiple Sclerosis and Related Disorders, bind 77, 104854. https://doi.org/10.1016/j.msard.2023.104854

APA

Ammitzbøll, C., Dyrby, T. B., Börnsen, L., Schreiber, K., Ratzer, R., Romme Christensen, J., Iversen, P., Magyari, M., Lundell, H., Jensen, P. E. H., Sørensen, P. S., Siebner, H. R., & Sellebjerg, F. (2023). NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis. Multiple Sclerosis and Related Disorders, 77, [104854]. https://doi.org/10.1016/j.msard.2023.104854

Vancouver

Ammitzbøll C, Dyrby TB, Börnsen L, Schreiber K, Ratzer R, Romme Christensen J o.a. NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis. Multiple Sclerosis and Related Disorders. 2023;77. 104854. https://doi.org/10.1016/j.msard.2023.104854

Author

Ammitzbøll, C. ; Dyrby, T. B. ; Börnsen, L. ; Schreiber, K. ; Ratzer, R. ; Romme Christensen, J. ; Iversen, P. ; Magyari, M. ; Lundell, H. ; Jensen, P. E.H. ; Sørensen, P. S. ; Siebner, H. R. ; Sellebjerg, F. / NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis. I: Multiple Sclerosis and Related Disorders. 2023 ; Bind 77.

Bibtex

@article{99349eac5e184178ba48b612753399fb,
title = "NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis",
abstract = "Background: The potential of neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) as biomarkers of disease activity and severity in progressive forms of multiple sclerosis (MS) is unclear. Objective: To investigate the relationship between serum concentrations of NfL, GFAP, and magnetic resonance imaging (MRI) in progressive MS. Methods: Serum concentrations of NfL and GFAP were measured in 32 healthy controls and 32 patients with progressive MS from whom clinical and MRI data including diffusion tensor imaging (DTI) were obtained during three years of follow-up. Results: Serum concentrations of NfL and GFAP at follow-up were higher in progressive MS patients than in healthy controls and serum NfL correlated with the EDSS score. Decreasing fractional anisotropy (FA) in normal-appearing white matter (NAWM) correlated with worsening EDSS scores and higher serum NfL. Higher serum NfL and increasing T2 lesion volume correlated with worsening paced autitory serial addition test scores. In multivariable regression analyses with serum GFAP and NfL as independent factors and DTI measures of NAWM as dependent factors, we showed that high serum NfL at follow-up was independently associated with decreasing FA and increasing MD in NAWM. Moreover, we found that high serum GFAP was independently associated with decreasing MD in NAWM and with decreasing MD and increasing FA in cortical gray matter. Conclusion: Serum concentrations of NfL and GFAP are increased in progressive MS and are associated with distinct microstructural changes in NAWM and CGM.",
keywords = "Diffusion tensor imaging, Glial fibrillary acidic protein, Magnetic resonance imaging, Multiple sclerosis, Neurofilament light chain",
author = "C. Ammitzb{\o}ll and Dyrby, {T. B.} and L. B{\"o}rnsen and K. Schreiber and R. Ratzer and {Romme Christensen}, J. and P. Iversen and M. Magyari and H. Lundell and Jensen, {P. E.H.} and S{\o}rensen, {P. S.} and Siebner, {H. R.} and F. Sellebjerg",
note = "Publisher Copyright: {\textcopyright} 2023",
year = "2023",
doi = "10.1016/j.msard.2023.104854",
language = "English",
volume = "77",
journal = "Multiple Sclerosis and Related Disorders",
issn = "2211-0348",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - NfL and GFAP in serum are associated with microstructural brain damage in progressive multiple sclerosis

AU - Ammitzbøll, C.

AU - Dyrby, T. B.

AU - Börnsen, L.

AU - Schreiber, K.

AU - Ratzer, R.

AU - Romme Christensen, J.

AU - Iversen, P.

AU - Magyari, M.

AU - Lundell, H.

AU - Jensen, P. E.H.

AU - Sørensen, P. S.

AU - Siebner, H. R.

AU - Sellebjerg, F.

N1 - Publisher Copyright: © 2023

PY - 2023

Y1 - 2023

N2 - Background: The potential of neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) as biomarkers of disease activity and severity in progressive forms of multiple sclerosis (MS) is unclear. Objective: To investigate the relationship between serum concentrations of NfL, GFAP, and magnetic resonance imaging (MRI) in progressive MS. Methods: Serum concentrations of NfL and GFAP were measured in 32 healthy controls and 32 patients with progressive MS from whom clinical and MRI data including diffusion tensor imaging (DTI) were obtained during three years of follow-up. Results: Serum concentrations of NfL and GFAP at follow-up were higher in progressive MS patients than in healthy controls and serum NfL correlated with the EDSS score. Decreasing fractional anisotropy (FA) in normal-appearing white matter (NAWM) correlated with worsening EDSS scores and higher serum NfL. Higher serum NfL and increasing T2 lesion volume correlated with worsening paced autitory serial addition test scores. In multivariable regression analyses with serum GFAP and NfL as independent factors and DTI measures of NAWM as dependent factors, we showed that high serum NfL at follow-up was independently associated with decreasing FA and increasing MD in NAWM. Moreover, we found that high serum GFAP was independently associated with decreasing MD in NAWM and with decreasing MD and increasing FA in cortical gray matter. Conclusion: Serum concentrations of NfL and GFAP are increased in progressive MS and are associated with distinct microstructural changes in NAWM and CGM.

AB - Background: The potential of neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) as biomarkers of disease activity and severity in progressive forms of multiple sclerosis (MS) is unclear. Objective: To investigate the relationship between serum concentrations of NfL, GFAP, and magnetic resonance imaging (MRI) in progressive MS. Methods: Serum concentrations of NfL and GFAP were measured in 32 healthy controls and 32 patients with progressive MS from whom clinical and MRI data including diffusion tensor imaging (DTI) were obtained during three years of follow-up. Results: Serum concentrations of NfL and GFAP at follow-up were higher in progressive MS patients than in healthy controls and serum NfL correlated with the EDSS score. Decreasing fractional anisotropy (FA) in normal-appearing white matter (NAWM) correlated with worsening EDSS scores and higher serum NfL. Higher serum NfL and increasing T2 lesion volume correlated with worsening paced autitory serial addition test scores. In multivariable regression analyses with serum GFAP and NfL as independent factors and DTI measures of NAWM as dependent factors, we showed that high serum NfL at follow-up was independently associated with decreasing FA and increasing MD in NAWM. Moreover, we found that high serum GFAP was independently associated with decreasing MD in NAWM and with decreasing MD and increasing FA in cortical gray matter. Conclusion: Serum concentrations of NfL and GFAP are increased in progressive MS and are associated with distinct microstructural changes in NAWM and CGM.

KW - Diffusion tensor imaging

KW - Glial fibrillary acidic protein

KW - Magnetic resonance imaging

KW - Multiple sclerosis

KW - Neurofilament light chain

U2 - 10.1016/j.msard.2023.104854

DO - 10.1016/j.msard.2023.104854

M3 - Journal article

C2 - 37418931

AN - SCOPUS:85165294265

VL - 77

JO - Multiple Sclerosis and Related Disorders

JF - Multiple Sclerosis and Related Disorders

SN - 2211-0348

M1 - 104854

ER -

ID: 360398220