Cargando…
Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis
BACKGROUND AND OBJECTIVES: Cortical lesions (CL) are common in multiple sclerosis (MS) and associate with disability and progressive disease. We asked whether CL continue to form in people with stable white matter lesions (WML) and whether the association of CL with worsening disability relates to p...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602044/ https://www.ncbi.nlm.nih.gov/pubmed/37886541 http://dx.doi.org/10.1101/2023.09.22.23295974 |
_version_ | 1785126311809777664 |
---|---|
author | Beck, Erin S Mullins, W Andrew dos Santos Silva, Jonadab Filippini, Stefano Parvathaneni, Prasanna Maranzano, Josefina Morrison, Mark Suto, Daniel J Donnay, Corinne Dieckhaus, Henry Luciano, Nicholas J Sharma, Kanika Gaitán, María Ines Liu, Jiaen de Zwart, Jacco A van Gelderen, Peter Cortese, Irene Narayanan, Sridar Duyn, Jeff H Nair, Govind Sati, Pascal Reich, Daniel S |
author_facet | Beck, Erin S Mullins, W Andrew dos Santos Silva, Jonadab Filippini, Stefano Parvathaneni, Prasanna Maranzano, Josefina Morrison, Mark Suto, Daniel J Donnay, Corinne Dieckhaus, Henry Luciano, Nicholas J Sharma, Kanika Gaitán, María Ines Liu, Jiaen de Zwart, Jacco A van Gelderen, Peter Cortese, Irene Narayanan, Sridar Duyn, Jeff H Nair, Govind Sati, Pascal Reich, Daniel S |
author_sort | Beck, Erin S |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Cortical lesions (CL) are common in multiple sclerosis (MS) and associate with disability and progressive disease. We asked whether CL continue to form in people with stable white matter lesions (WML) and whether the association of CL with worsening disability relates to pre-existing or new CL. METHODS: A cohort of adults with MS were evaluated annually with 7 tesla (T) brain magnetic resonance imaging (MRI) and 3T brain and spine MRI for 2 years, and clinical assessments for 3 years. CL were identified on 7T images at each timepoint. WML and brain tissue segmentation were performed using 3T images at baseline and year 2. RESULTS: 59 adults with MS had ≥1 7T follow-up visit (mean follow-up time 2±0.5 years). 9 had “active” relapsing-remitting MS (RRMS), defined as new WML in the year prior to enrollment. Of the remaining 50, 33 had “stable” RRMS, 14 secondary progressive MS (SPMS), and 3 primary progressive MS. 16 total new CL formed in the active RRMS group (median 1, range 0–10), 7 in the stable RRMS group (median 0, range 0–5), and 4 in the progressive MS group (median 0, range 0–1) (p=0.006, stable RR vs PMS p=0.88). New CL were not associated with greater change in any individual disability measure or in a composite measure of disability worsening (worsening Expanded Disability Status Scale or 9-hole peg test or 25-foot timed walk). Baseline CL volume was higher in people with worsening disability (median 1010μl, range 13–9888 vs median 267μl, range 0–3539, p=0.001, adjusted for age and sex) and in individuals with RRMS who subsequently transitioned to SPMS (median 2183μl, range 270–9888 vs median 321μl, range 0–6392 in those who remained RRMS, p=0.01, adjusted for age and sex). Baseline WML volume was not associated with worsening disability or transition from RRMS to SPMS. DISCUSSION: CL formation is rare in people with stable WML, even in those with worsening disability. CL but not WML burden predicts future worsening of disability, suggesting that the relationship between CL and disability progression is related to long-term effects of lesions that form in the earlier stages of disease, rather than to ongoing lesion formation. |
format | Online Article Text |
id | pubmed-10602044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106020442023-10-27 Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis Beck, Erin S Mullins, W Andrew dos Santos Silva, Jonadab Filippini, Stefano Parvathaneni, Prasanna Maranzano, Josefina Morrison, Mark Suto, Daniel J Donnay, Corinne Dieckhaus, Henry Luciano, Nicholas J Sharma, Kanika Gaitán, María Ines Liu, Jiaen de Zwart, Jacco A van Gelderen, Peter Cortese, Irene Narayanan, Sridar Duyn, Jeff H Nair, Govind Sati, Pascal Reich, Daniel S medRxiv Article BACKGROUND AND OBJECTIVES: Cortical lesions (CL) are common in multiple sclerosis (MS) and associate with disability and progressive disease. We asked whether CL continue to form in people with stable white matter lesions (WML) and whether the association of CL with worsening disability relates to pre-existing or new CL. METHODS: A cohort of adults with MS were evaluated annually with 7 tesla (T) brain magnetic resonance imaging (MRI) and 3T brain and spine MRI for 2 years, and clinical assessments for 3 years. CL were identified on 7T images at each timepoint. WML and brain tissue segmentation were performed using 3T images at baseline and year 2. RESULTS: 59 adults with MS had ≥1 7T follow-up visit (mean follow-up time 2±0.5 years). 9 had “active” relapsing-remitting MS (RRMS), defined as new WML in the year prior to enrollment. Of the remaining 50, 33 had “stable” RRMS, 14 secondary progressive MS (SPMS), and 3 primary progressive MS. 16 total new CL formed in the active RRMS group (median 1, range 0–10), 7 in the stable RRMS group (median 0, range 0–5), and 4 in the progressive MS group (median 0, range 0–1) (p=0.006, stable RR vs PMS p=0.88). New CL were not associated with greater change in any individual disability measure or in a composite measure of disability worsening (worsening Expanded Disability Status Scale or 9-hole peg test or 25-foot timed walk). Baseline CL volume was higher in people with worsening disability (median 1010μl, range 13–9888 vs median 267μl, range 0–3539, p=0.001, adjusted for age and sex) and in individuals with RRMS who subsequently transitioned to SPMS (median 2183μl, range 270–9888 vs median 321μl, range 0–6392 in those who remained RRMS, p=0.01, adjusted for age and sex). Baseline WML volume was not associated with worsening disability or transition from RRMS to SPMS. DISCUSSION: CL formation is rare in people with stable WML, even in those with worsening disability. CL but not WML burden predicts future worsening of disability, suggesting that the relationship between CL and disability progression is related to long-term effects of lesions that form in the earlier stages of disease, rather than to ongoing lesion formation. Cold Spring Harbor Laboratory 2023-09-25 /pmc/articles/PMC10602044/ /pubmed/37886541 http://dx.doi.org/10.1101/2023.09.22.23295974 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Article Beck, Erin S Mullins, W Andrew dos Santos Silva, Jonadab Filippini, Stefano Parvathaneni, Prasanna Maranzano, Josefina Morrison, Mark Suto, Daniel J Donnay, Corinne Dieckhaus, Henry Luciano, Nicholas J Sharma, Kanika Gaitán, María Ines Liu, Jiaen de Zwart, Jacco A van Gelderen, Peter Cortese, Irene Narayanan, Sridar Duyn, Jeff H Nair, Govind Sati, Pascal Reich, Daniel S Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis |
title | Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis |
title_full | Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis |
title_fullStr | Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis |
title_full_unstemmed | Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis |
title_short | Cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis |
title_sort | cortical lesions uniquely predict motor disability accrual and form rarely in the absence of new white matter lesions in multiple sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602044/ https://www.ncbi.nlm.nih.gov/pubmed/37886541 http://dx.doi.org/10.1101/2023.09.22.23295974 |
work_keys_str_mv | AT beckerins corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT mullinswandrew corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT dossantossilvajonadab corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT filippinistefano corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT parvathaneniprasanna corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT maranzanojosefina corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT morrisonmark corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT sutodanielj corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT donnaycorinne corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT dieckhaushenry corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT lucianonicholasj corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT sharmakanika corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT gaitanmariaines corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT liujiaen corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT dezwartjaccoa corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT vangelderenpeter corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT corteseirene corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT narayanansridar corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT duynjeffh corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT nairgovind corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT satipascal corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis AT reichdaniels corticallesionsuniquelypredictmotordisabilityaccrualandformrarelyintheabsenceofnewwhitematterlesionsinmultiplesclerosis |