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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
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
Descripción
Sumario: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.