TY - JOUR
T1 - Plasma neurofilament light admission levels and development of axonal pathology in mild traumatic brain injury
AU - Hossain, Iftakher
AU - Mohammadian, Mehrbod
AU - Maanpää, Henna Riikka
AU - Takala, Riikka S.K.
AU - Tenovuo, Olli
AU - van Gils, Mark
AU - Hutchinson, Peter
AU - Menon, David K.
AU - Newcombe, Virginia F.
AU - Tallus, Jussi
AU - Hirvonen, Jussi
AU - Roine, Timo
AU - Kurki, Timo
AU - Blennow, Kaj
AU - Zetterberg, Henrik
AU - Posti, Jussi P.
N1 - Publisher Copyright:
© 2023. BioMed Central Ltd., part of Springer Nature.
PY - 2023/8/15
Y1 - 2023/8/15
N2 - BACKGROUND: It is known that blood levels of neurofilament light (NF-L) and diffusion-weighted magnetic resonance imaging (DW-MRI) are both associated with outcome of patients with mild traumatic brain injury (mTBI). Here, we sought to examine the association between admission levels of plasma NF-L and white matter (WM) integrity in post-acute stage DW-MRI in patients with mTBI. METHODS: Ninety-three patients with mTBI (GCS ≥ 13), blood sample for NF-L within 24 h of admission, and DW-MRI ≥ 90 days post-injury (median = 229) were included. Mean fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) were calculated from the skeletonized WM tracts of the whole brain. Outcome was assessed using the Extended Glasgow Outcome Scale (GOSE) at the time of imaging. Patients were divided into CT-positive and -negative, and complete (GOSE = 8) and incomplete recovery (GOSE < 8) groups. RESULTS: The levels of NF-L and FA correlated negatively in the whole cohort (p = 0.002), in CT-positive patients (p = 0.016), and in those with incomplete recovery (p = 0.005). The same groups showed a positive correlation with mean MD, AD, and RD (p < 0.001-p = 0.011). In CT-negative patients or in patients with full recovery, significant correlations were not found. CONCLUSION: In patients with mTBI, the significant correlation between NF-L levels at admission and diffusion tensor imaging (DTI) measurements of diffuse axonal injury (DAI) over more than 3 months suggests that the early levels of plasma NF-L may associate with the presence of DAI at a later phase of TBI.
AB - BACKGROUND: It is known that blood levels of neurofilament light (NF-L) and diffusion-weighted magnetic resonance imaging (DW-MRI) are both associated with outcome of patients with mild traumatic brain injury (mTBI). Here, we sought to examine the association between admission levels of plasma NF-L and white matter (WM) integrity in post-acute stage DW-MRI in patients with mTBI. METHODS: Ninety-three patients with mTBI (GCS ≥ 13), blood sample for NF-L within 24 h of admission, and DW-MRI ≥ 90 days post-injury (median = 229) were included. Mean fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) were calculated from the skeletonized WM tracts of the whole brain. Outcome was assessed using the Extended Glasgow Outcome Scale (GOSE) at the time of imaging. Patients were divided into CT-positive and -negative, and complete (GOSE = 8) and incomplete recovery (GOSE < 8) groups. RESULTS: The levels of NF-L and FA correlated negatively in the whole cohort (p = 0.002), in CT-positive patients (p = 0.016), and in those with incomplete recovery (p = 0.005). The same groups showed a positive correlation with mean MD, AD, and RD (p < 0.001-p = 0.011). In CT-negative patients or in patients with full recovery, significant correlations were not found. CONCLUSION: In patients with mTBI, the significant correlation between NF-L levels at admission and diffusion tensor imaging (DTI) measurements of diffuse axonal injury (DAI) over more than 3 months suggests that the early levels of plasma NF-L may associate with the presence of DAI at a later phase of TBI.
KW - Diffusion tensor imaging
KW - Diffusion-weighted magnetic resonance imaging
KW - Neurofilament light protein
UR - http://www.scopus.com/inward/record.url?scp=85168063555&partnerID=8YFLogxK
U2 - 10.1186/s12883-023-03284-6
DO - 10.1186/s12883-023-03284-6
M3 - Article
C2 - 37582732
AN - SCOPUS:85168063555
SN - 1471-2377
VL - 23
SP - 1
EP - 12
JO - BMC Neurology
JF - BMC Neurology
IS - 1
M1 - 304
ER -