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Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T
BACKGROUND: Imaging investigation of cerebrospinal fluid (CSF) in multiple sclerosis (MS) is understudied. Development of noninvasive methods to detect pathological CSF changes would have a profound effect on MS diagnosis and would offer insight into MS pathophysiology and mechanisms of neurological...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644741/ https://www.ncbi.nlm.nih.gov/pubmed/38021451 http://dx.doi.org/10.1177/20552173231211396 |
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author | Lawless, Richard D McKnight, Colin D O’Grady, Kristin P Combes, Anna JE Rogers, Baxter P Witt, Atlee A Visagie, Mereze Houston, Delaney C Prock, Logan E Bagnato, Francesca R Smith, Seth A |
author_facet | Lawless, Richard D McKnight, Colin D O’Grady, Kristin P Combes, Anna JE Rogers, Baxter P Witt, Atlee A Visagie, Mereze Houston, Delaney C Prock, Logan E Bagnato, Francesca R Smith, Seth A |
author_sort | Lawless, Richard D |
collection | PubMed |
description | BACKGROUND: Imaging investigation of cerebrospinal fluid (CSF) in multiple sclerosis (MS) is understudied. Development of noninvasive methods to detect pathological CSF changes would have a profound effect on MS diagnosis and would offer insight into MS pathophysiology and mechanisms of neurological impairment. OBJECTIVE: We propose magnetization transfer (MT) MRI as a tool to detect macromolecular changes in spinal CSF. METHODS: MT and quantitative MT (qMT) data were acquired in the cervical region in 27 people with relapsing-remitting multiple sclerosis (pwRRMS) and 38 age and sex-matched healthy controls (HCs). MT ratio (MTR), the B(1), B(0), and R(1) corrected qMT-derived pool size ratio (PSR) were quantified in the spinal cord and CSF of each group. RESULTS: Both CSF MTR and CSF qMT-derived PSR were significantly increased in pwRRMS compared to HC (p = 0.027 and p = 0.020, respectively). CSF PSR of pwRRMS was correlated to Expanded Disability Status Scale Scores (p = 0.045, R = 0.352). CONCLUSION: Our findings demonstrate increased CSF macromolecular content in pwRRMS and link CSF macromolecular content with clinical impairment. This highlights the potential role of CSF in processing products of demyelination. |
format | Online Article Text |
id | pubmed-10644741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-106447412023-11-13 Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T Lawless, Richard D McKnight, Colin D O’Grady, Kristin P Combes, Anna JE Rogers, Baxter P Witt, Atlee A Visagie, Mereze Houston, Delaney C Prock, Logan E Bagnato, Francesca R Smith, Seth A Mult Scler J Exp Transl Clin Original Research Article BACKGROUND: Imaging investigation of cerebrospinal fluid (CSF) in multiple sclerosis (MS) is understudied. Development of noninvasive methods to detect pathological CSF changes would have a profound effect on MS diagnosis and would offer insight into MS pathophysiology and mechanisms of neurological impairment. OBJECTIVE: We propose magnetization transfer (MT) MRI as a tool to detect macromolecular changes in spinal CSF. METHODS: MT and quantitative MT (qMT) data were acquired in the cervical region in 27 people with relapsing-remitting multiple sclerosis (pwRRMS) and 38 age and sex-matched healthy controls (HCs). MT ratio (MTR), the B(1), B(0), and R(1) corrected qMT-derived pool size ratio (PSR) were quantified in the spinal cord and CSF of each group. RESULTS: Both CSF MTR and CSF qMT-derived PSR were significantly increased in pwRRMS compared to HC (p = 0.027 and p = 0.020, respectively). CSF PSR of pwRRMS was correlated to Expanded Disability Status Scale Scores (p = 0.045, R = 0.352). CONCLUSION: Our findings demonstrate increased CSF macromolecular content in pwRRMS and link CSF macromolecular content with clinical impairment. This highlights the potential role of CSF in processing products of demyelination. SAGE Publications 2023-11-13 /pmc/articles/PMC10644741/ /pubmed/38021451 http://dx.doi.org/10.1177/20552173231211396 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Article Lawless, Richard D McKnight, Colin D O’Grady, Kristin P Combes, Anna JE Rogers, Baxter P Witt, Atlee A Visagie, Mereze Houston, Delaney C Prock, Logan E Bagnato, Francesca R Smith, Seth A Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T |
title | Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T |
title_full | Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T |
title_fullStr | Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T |
title_full_unstemmed | Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T |
title_short | Detecting macromolecular differences of the CSF in low disability multiple sclerosis using quantitative MT MRI at 3T |
title_sort | detecting macromolecular differences of the csf in low disability multiple sclerosis using quantitative mt mri at 3t |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644741/ https://www.ncbi.nlm.nih.gov/pubmed/38021451 http://dx.doi.org/10.1177/20552173231211396 |
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