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Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS

OBJECTIVE: The central vein sign (CVS) and “paramagnetic rim lesions” (PRL) are emerging imaging biomarkers in multiple sclerosis (MS) reflecting perivenular demyelination and chronic, smoldering inflammation. The objective of this study was to assess relationships between cognitive impairment (CI)...

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Autores principales: Oh, Jiwon, Suthiphosuwan, Suradech, Sati, Pascal, Absinta, Martina, Dewey, Blake, Guenette, Melanie, Selchen, Daniel, Bharatha, Aditya, Donaldson, Emily, Reich, Daniel S, Feinstein, Anthony
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458475/
https://www.ncbi.nlm.nih.gov/pubmed/33754887
http://dx.doi.org/10.1177/13524585211002097
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author Oh, Jiwon
Suthiphosuwan, Suradech
Sati, Pascal
Absinta, Martina
Dewey, Blake
Guenette, Melanie
Selchen, Daniel
Bharatha, Aditya
Donaldson, Emily
Reich, Daniel S
Feinstein, Anthony
author_facet Oh, Jiwon
Suthiphosuwan, Suradech
Sati, Pascal
Absinta, Martina
Dewey, Blake
Guenette, Melanie
Selchen, Daniel
Bharatha, Aditya
Donaldson, Emily
Reich, Daniel S
Feinstein, Anthony
author_sort Oh, Jiwon
collection PubMed
description OBJECTIVE: The central vein sign (CVS) and “paramagnetic rim lesions” (PRL) are emerging imaging biomarkers in multiple sclerosis (MS) reflecting perivenular demyelination and chronic, smoldering inflammation. The objective of this study was to assess relationships between cognitive impairment (CI) and the CVS and PRL in radiologically isolated syndrome (RIS). METHODS: Twenty-seven adults with RIS underwent 3.0 T MRI of the brain and cervical spinal cord (SC) and cognitive assessment using the minimal assessment of cognitive function in MS battery. The CVS and PRL were assessed in white-matter lesions (WMLs) on T2*-weighted segmented echo-planar magnitude and phase images. Multivariable linear regression evaluated relationships between CI and MRI measures. RESULTS: Global CI was present in 9 (33%) participants with processing speed and visual memory most frequently affected. Most participants (93%) had ⩾ 40% CVS + WML (a threshold distinguishing MS from other WM disorders); 63% demonstrated PRL. Linear regression revealed that CVS + WML predicted performance on verbal memory(β =-0.024, p = 0.03) while PRL predicted performance on verbal memory (β = -0.040, p = 0.04) and processing speed (β = -0.039, p = 0.03). CONCLUSIONS: CI is common in RIS and is associated with markers of perivenular demyelination and chronic inflammation in WML, such as CVS + WML and PRL. A prospective follow-up of this cohort will ascertain the importance of CI, CVS, and PRL as risk factors for conversion from RIS to MS.
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spelling pubmed-84584752021-11-18 Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS Oh, Jiwon Suthiphosuwan, Suradech Sati, Pascal Absinta, Martina Dewey, Blake Guenette, Melanie Selchen, Daniel Bharatha, Aditya Donaldson, Emily Reich, Daniel S Feinstein, Anthony Mult Scler Original Research Papers OBJECTIVE: The central vein sign (CVS) and “paramagnetic rim lesions” (PRL) are emerging imaging biomarkers in multiple sclerosis (MS) reflecting perivenular demyelination and chronic, smoldering inflammation. The objective of this study was to assess relationships between cognitive impairment (CI) and the CVS and PRL in radiologically isolated syndrome (RIS). METHODS: Twenty-seven adults with RIS underwent 3.0 T MRI of the brain and cervical spinal cord (SC) and cognitive assessment using the minimal assessment of cognitive function in MS battery. The CVS and PRL were assessed in white-matter lesions (WMLs) on T2*-weighted segmented echo-planar magnitude and phase images. Multivariable linear regression evaluated relationships between CI and MRI measures. RESULTS: Global CI was present in 9 (33%) participants with processing speed and visual memory most frequently affected. Most participants (93%) had ⩾ 40% CVS + WML (a threshold distinguishing MS from other WM disorders); 63% demonstrated PRL. Linear regression revealed that CVS + WML predicted performance on verbal memory(β =-0.024, p = 0.03) while PRL predicted performance on verbal memory (β = -0.040, p = 0.04) and processing speed (β = -0.039, p = 0.03). CONCLUSIONS: CI is common in RIS and is associated with markers of perivenular demyelination and chronic inflammation in WML, such as CVS + WML and PRL. A prospective follow-up of this cohort will ascertain the importance of CI, CVS, and PRL as risk factors for conversion from RIS to MS. SAGE Publications 2021-03-23 2021-12 /pmc/articles/PMC8458475/ /pubmed/33754887 http://dx.doi.org/10.1177/13524585211002097 Text en © The Author(s), 2021 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 Papers
Oh, Jiwon
Suthiphosuwan, Suradech
Sati, Pascal
Absinta, Martina
Dewey, Blake
Guenette, Melanie
Selchen, Daniel
Bharatha, Aditya
Donaldson, Emily
Reich, Daniel S
Feinstein, Anthony
Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS
title Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS
title_full Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS
title_fullStr Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS
title_full_unstemmed Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS
title_short Cognitive impairment, the central vein sign, and paramagnetic rim lesions in RIS
title_sort cognitive impairment, the central vein sign, and paramagnetic rim lesions in ris
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8458475/
https://www.ncbi.nlm.nih.gov/pubmed/33754887
http://dx.doi.org/10.1177/13524585211002097
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