Cargando…
Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity
The glymphatic system is a perivascular fluid clearance system, most active during sleep, considered important for clearing the brain of waste products and toxins. Glymphatic failure is hypothesized to underlie brain protein deposition in neurodegenerative disorders like Alzheimer’s disease. Preclin...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176239/ https://www.ncbi.nlm.nih.gov/pubmed/37188222 http://dx.doi.org/10.1093/braincomms/fcad134 |
_version_ | 1785040389428740096 |
---|---|
author | Butler, Tracy Zhou, Liangdong Ozsahin, Ilker Wang, Xiuyuan Hugh Garetti, Jacob Zetterberg, Henrik Blennow, Kaj Jamison, Keith de Leon, Mony J Li, Yi Kuceyeski, Amy Shah, Sudhin A |
author_facet | Butler, Tracy Zhou, Liangdong Ozsahin, Ilker Wang, Xiuyuan Hugh Garetti, Jacob Zetterberg, Henrik Blennow, Kaj Jamison, Keith de Leon, Mony J Li, Yi Kuceyeski, Amy Shah, Sudhin A |
author_sort | Butler, Tracy |
collection | PubMed |
description | The glymphatic system is a perivascular fluid clearance system, most active during sleep, considered important for clearing the brain of waste products and toxins. Glymphatic failure is hypothesized to underlie brain protein deposition in neurodegenerative disorders like Alzheimer’s disease. Preclinical evidence suggests that a functioning glymphatic system is also essential for recovery from traumatic brain injury, which involves release of debris and toxic proteins that need to be cleared from the brain. In a cross-sectional observational study, we estimated glymphatic clearance using diffusion tensor imaging along perivascular spaces, an MRI-derived measure of water diffusivity surrounding veins in the periventricular region, in 13 non-injured controls and 37 subjects who had experienced traumatic brain injury ∼5 months previously. We additionally measured the volume of the perivascular space using T(2)-weighted MRI. We measured plasma concentrations of neurofilament light chain, a biomarker of injury severity, in a subset of subjects. Diffusion tensor imaging along perivascular spaces index was modestly though significantly lower in subjects with traumatic brain injury compared with controls when covarying for age. Diffusion tensor imaging along perivascular spaces index was significantly, negatively correlated with blood levels of neurofilament light chain. Perivascular space volume did not differ in subjects with traumatic brain injury as compared with controls and did not correlate with blood levels of neurofilament light chain, suggesting it may be a less sensitive measure for injury-related perivascular clearance changes. Glymphatic impairment after traumatic brain injury could be due to mechanisms such as mislocalization of glymphatic water channels, inflammation, proteinopathy and/or sleep disruption. Diffusion tensor imaging along perivascular spaces is a promising method for estimating glymphatic clearance, though additional work is needed to confirm results and assess associations with outcome. Understanding changes in glymphatic functioning following traumatic brain injury could inform novel therapies to improve short-term recovery and reduce later risk of neurodegeneration. |
format | Online Article Text |
id | pubmed-10176239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101762392023-05-13 Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity Butler, Tracy Zhou, Liangdong Ozsahin, Ilker Wang, Xiuyuan Hugh Garetti, Jacob Zetterberg, Henrik Blennow, Kaj Jamison, Keith de Leon, Mony J Li, Yi Kuceyeski, Amy Shah, Sudhin A Brain Commun Original Article The glymphatic system is a perivascular fluid clearance system, most active during sleep, considered important for clearing the brain of waste products and toxins. Glymphatic failure is hypothesized to underlie brain protein deposition in neurodegenerative disorders like Alzheimer’s disease. Preclinical evidence suggests that a functioning glymphatic system is also essential for recovery from traumatic brain injury, which involves release of debris and toxic proteins that need to be cleared from the brain. In a cross-sectional observational study, we estimated glymphatic clearance using diffusion tensor imaging along perivascular spaces, an MRI-derived measure of water diffusivity surrounding veins in the periventricular region, in 13 non-injured controls and 37 subjects who had experienced traumatic brain injury ∼5 months previously. We additionally measured the volume of the perivascular space using T(2)-weighted MRI. We measured plasma concentrations of neurofilament light chain, a biomarker of injury severity, in a subset of subjects. Diffusion tensor imaging along perivascular spaces index was modestly though significantly lower in subjects with traumatic brain injury compared with controls when covarying for age. Diffusion tensor imaging along perivascular spaces index was significantly, negatively correlated with blood levels of neurofilament light chain. Perivascular space volume did not differ in subjects with traumatic brain injury as compared with controls and did not correlate with blood levels of neurofilament light chain, suggesting it may be a less sensitive measure for injury-related perivascular clearance changes. Glymphatic impairment after traumatic brain injury could be due to mechanisms such as mislocalization of glymphatic water channels, inflammation, proteinopathy and/or sleep disruption. Diffusion tensor imaging along perivascular spaces is a promising method for estimating glymphatic clearance, though additional work is needed to confirm results and assess associations with outcome. Understanding changes in glymphatic functioning following traumatic brain injury could inform novel therapies to improve short-term recovery and reduce later risk of neurodegeneration. Oxford University Press 2023-04-25 /pmc/articles/PMC10176239/ /pubmed/37188222 http://dx.doi.org/10.1093/braincomms/fcad134 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Butler, Tracy Zhou, Liangdong Ozsahin, Ilker Wang, Xiuyuan Hugh Garetti, Jacob Zetterberg, Henrik Blennow, Kaj Jamison, Keith de Leon, Mony J Li, Yi Kuceyeski, Amy Shah, Sudhin A Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity |
title | Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity |
title_full | Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity |
title_fullStr | Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity |
title_full_unstemmed | Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity |
title_short | Glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity |
title_sort | glymphatic clearance estimated using diffusion tensor imaging along perivascular spaces is reduced after traumatic brain injury and correlates with plasma neurofilament light, a biomarker of injury severity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176239/ https://www.ncbi.nlm.nih.gov/pubmed/37188222 http://dx.doi.org/10.1093/braincomms/fcad134 |
work_keys_str_mv | AT butlertracy glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT zhouliangdong glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT ozsahinilker glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT wangxiuyuanhugh glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT garettijacob glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT zetterberghenrik glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT blennowkaj glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT jamisonkeith glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT deleonmonyj glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT liyi glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT kuceyeskiamy glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity AT shahsudhina glymphaticclearanceestimatedusingdiffusiontensorimagingalongperivascularspacesisreducedaftertraumaticbraininjuryandcorrelateswithplasmaneurofilamentlightabiomarkerofinjuryseverity |