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Serum neurofilament light chain levels associations with gray matter pathology: a 5‐year longitudinal study
by
Dwyer, Michael G.
, Benedict, Ralph H. B.
, Michalak, Zuzanna
, Weinstock‐Guttman, Bianca
, Tomic, Davorka
, Jakimovski, Dejan
, Kuhle, Jens
, Kropshofer, Harald
, Ramanathan, Murali
, Zivadinov, Robert
, Barro, Christian
, Leppert, David
, Hagemeier, Jesper
, Bergsland, Niels
in
Adult
/ Atrophy
/ Biomarkers
/ Brain - diagnostic imaging
/ Brain - pathology
/ Brain research
/ Disease
/ Disease Progression
/ Female
/ Gray Matter - diagnostic imaging
/ Gray Matter - pathology
/ Humans
/ Intermediate Filaments
/ Longitudinal Studies
/ Magnetic Resonance Imaging
/ Male
/ Middle Aged
/ Multiple sclerosis
/ Multiple Sclerosis - blood
/ Multiple Sclerosis - diagnostic imaging
/ Multiple Sclerosis - pathology
/ Neurodegeneration
/ Neurofilament Proteins - blood
/ NMR
/ Nuclear magnetic resonance
/ Pathology
/ Supervision
2019
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Serum neurofilament light chain levels associations with gray matter pathology: a 5‐year longitudinal study
by
Dwyer, Michael G.
, Benedict, Ralph H. B.
, Michalak, Zuzanna
, Weinstock‐Guttman, Bianca
, Tomic, Davorka
, Jakimovski, Dejan
, Kuhle, Jens
, Kropshofer, Harald
, Ramanathan, Murali
, Zivadinov, Robert
, Barro, Christian
, Leppert, David
, Hagemeier, Jesper
, Bergsland, Niels
in
Adult
/ Atrophy
/ Biomarkers
/ Brain - diagnostic imaging
/ Brain - pathology
/ Brain research
/ Disease
/ Disease Progression
/ Female
/ Gray Matter - diagnostic imaging
/ Gray Matter - pathology
/ Humans
/ Intermediate Filaments
/ Longitudinal Studies
/ Magnetic Resonance Imaging
/ Male
/ Middle Aged
/ Multiple sclerosis
/ Multiple Sclerosis - blood
/ Multiple Sclerosis - diagnostic imaging
/ Multiple Sclerosis - pathology
/ Neurodegeneration
/ Neurofilament Proteins - blood
/ NMR
/ Nuclear magnetic resonance
/ Pathology
/ Supervision
2019
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Serum neurofilament light chain levels associations with gray matter pathology: a 5‐year longitudinal study
by
Dwyer, Michael G.
, Benedict, Ralph H. B.
, Michalak, Zuzanna
, Weinstock‐Guttman, Bianca
, Tomic, Davorka
, Jakimovski, Dejan
, Kuhle, Jens
, Kropshofer, Harald
, Ramanathan, Murali
, Zivadinov, Robert
, Barro, Christian
, Leppert, David
, Hagemeier, Jesper
, Bergsland, Niels
in
Adult
/ Atrophy
/ Biomarkers
/ Brain - diagnostic imaging
/ Brain - pathology
/ Brain research
/ Disease
/ Disease Progression
/ Female
/ Gray Matter - diagnostic imaging
/ Gray Matter - pathology
/ Humans
/ Intermediate Filaments
/ Longitudinal Studies
/ Magnetic Resonance Imaging
/ Male
/ Middle Aged
/ Multiple sclerosis
/ Multiple Sclerosis - blood
/ Multiple Sclerosis - diagnostic imaging
/ Multiple Sclerosis - pathology
/ Neurodegeneration
/ Neurofilament Proteins - blood
/ NMR
/ Nuclear magnetic resonance
/ Pathology
/ Supervision
2019
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Serum neurofilament light chain levels associations with gray matter pathology: a 5‐year longitudinal study
Journal Article
Serum neurofilament light chain levels associations with gray matter pathology: a 5‐year longitudinal study
2019
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Overview
Background
Gray matter (GM) pathology is closely associated with physical and cognitive impairment in persons with multiple sclerosis (PwMS). Similarly, serum neurofilament light chain (sNfL) levels are related to MS disease activity and progression.
Objectives
To assess the cross–sectional and longitudinal associations between sNfL and MRI–derived lesion and brain volume outcomes in PwMS and age–matched healthy controls (HCs).
Materials and Methods
Forty‐seven HCs and 120 PwMS were followed over 5 years. All subjects underwent baseline and follow–up 3T MRI and sNfL examinations. Lesion volumes (LV) and global, tissue–specific and regional brain volumes were assessed. sNfL levels were analyzed using single molecule array (Simoa) assay and quantified in pg/mL. The associations between sNfL levels and MRI outcomes were investigated using regression analyses adjusted for age, sex, baseline disease modifying treatment (DMT) use and change in DMT over the follow‐up. False discovery rate (FDR)–adjusted q‐values <0.05 were considered significant.
Results
In PwMS, baseline sNfL was associated with baseline T1‐, T2‐ and gadolinium‐LV (q = 0.002, q = 0.001 and q < 0.001, respectively), but not with their longitudinal changes. Higher baseline sNfL levels were associated with lower baseline deep GM (β = −0.257, q = 0.017), thalamus (β = −0.216, q = 0.0017), caudate (β = −0.263, q = 0.014) and hippocampus (β = −0.267, q = 0.015) volumes. Baseline sNfL was associated with longitudinal decline of deep GM (β = −0.386, q < 0.001), putamen (β = −0.395, q < 0.001), whole brain (β = −0.356, q = 0.002), thalamus (β = −0.272, q = 0.049), globus pallidus (β = −0.284, q = 0.017), and GM (β = −0.264, q = 0.042) volumes. No associations between sNfL and MRI–derived measures were seen in the HCs.
Conclusion
Higher sNfL levels were associated with baseline LVs and greater development of GM atrophy in PwMS.
Publisher
John Wiley & Sons, Inc,John Wiley and Sons Inc,Wiley
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