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Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS

BACKGROUND: Multiple sclerosis is characterized by the formation of central nervous system demyelinating lesions with microvasculature inflammation. OBJECTIVE: Evaluate how lesion cerebral perfusion relates to white matter microstructural integrity in patients with RRMS using perfusion MRI and myeli...

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Autores principales: Sisco, Nicholas J, Borazanci, Aimee, Dortch, Richard, Stokes, Ashley M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330486/
https://www.ncbi.nlm.nih.gov/pubmed/34377529
http://dx.doi.org/10.1177/20552173211037002
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author Sisco, Nicholas J
Borazanci, Aimee
Dortch, Richard
Stokes, Ashley M
author_facet Sisco, Nicholas J
Borazanci, Aimee
Dortch, Richard
Stokes, Ashley M
author_sort Sisco, Nicholas J
collection PubMed
description BACKGROUND: Multiple sclerosis is characterized by the formation of central nervous system demyelinating lesions with microvasculature inflammation. OBJECTIVE: Evaluate how lesion cerebral perfusion relates to white matter microstructural integrity in patients with RRMS using perfusion MRI and myelin-related T(1)-weighted to T(2)-weighted (T(1)w/T(2)w) ratios. METHODS: Forty-eight patients with RRMS were imaged with dynamic susceptibility contrast imaging using SAGE (spin- and gradient-echo) to calculate global and capillary-sized perfusion parameters, including cerebral blood flow (CBF), volume (CBV), and mean transit time (MTT). T(1)w/T(2)w ratios were used to indirectly assess white matter microstructural integrity. RESULTS: For global perfusion metrics, CBF was reduced 28.4% in lesion regions of interest (ROIs) compared to normal appearing white matter (NAWM), CBV was reduced 25.9% in lesion ROIs compared to NAWM, and MTT increased 12.9%. For capillary perfusion metrics (via spin-echo (SE)), CBF-SE was reduced 35.7% in lesion ROIs compared to NAWM, CBV-SE was reduced 35.2% in lesion ROIs compared to NAWM, and MTT-SE increased 9.1%. Capillary-level CBF was correlated (ρ = 0.34, p = 0.024) with white matter microstructural integrity in lesion ROIs. CONCLUSION: This study demonstrates that lesion perfusion is reduced at both the global and capillary level and capillary-associated hypoperfusion is associated with reduced white matter microstructural integrity in RRMS.
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spelling pubmed-83304862021-08-09 Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS Sisco, Nicholas J Borazanci, Aimee Dortch, Richard Stokes, Ashley M Mult Scler J Exp Transl Clin Original Research Article BACKGROUND: Multiple sclerosis is characterized by the formation of central nervous system demyelinating lesions with microvasculature inflammation. OBJECTIVE: Evaluate how lesion cerebral perfusion relates to white matter microstructural integrity in patients with RRMS using perfusion MRI and myelin-related T(1)-weighted to T(2)-weighted (T(1)w/T(2)w) ratios. METHODS: Forty-eight patients with RRMS were imaged with dynamic susceptibility contrast imaging using SAGE (spin- and gradient-echo) to calculate global and capillary-sized perfusion parameters, including cerebral blood flow (CBF), volume (CBV), and mean transit time (MTT). T(1)w/T(2)w ratios were used to indirectly assess white matter microstructural integrity. RESULTS: For global perfusion metrics, CBF was reduced 28.4% in lesion regions of interest (ROIs) compared to normal appearing white matter (NAWM), CBV was reduced 25.9% in lesion ROIs compared to NAWM, and MTT increased 12.9%. For capillary perfusion metrics (via spin-echo (SE)), CBF-SE was reduced 35.7% in lesion ROIs compared to NAWM, CBV-SE was reduced 35.2% in lesion ROIs compared to NAWM, and MTT-SE increased 9.1%. Capillary-level CBF was correlated (ρ = 0.34, p = 0.024) with white matter microstructural integrity in lesion ROIs. CONCLUSION: This study demonstrates that lesion perfusion is reduced at both the global and capillary level and capillary-associated hypoperfusion is associated with reduced white matter microstructural integrity in RRMS. SAGE Publications 2021-07-29 /pmc/articles/PMC8330486/ /pubmed/34377529 http://dx.doi.org/10.1177/20552173211037002 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
Sisco, Nicholas J
Borazanci, Aimee
Dortch, Richard
Stokes, Ashley M
Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS
title Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS
title_full Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS
title_fullStr Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS
title_full_unstemmed Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS
title_short Investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting MS
title_sort investigating the relationship between multi-scale perfusion and white matter microstructural integrity in patients with relapsing-remitting ms
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330486/
https://www.ncbi.nlm.nih.gov/pubmed/34377529
http://dx.doi.org/10.1177/20552173211037002
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