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Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis
BACKGROUND: Previous research has shown that cerebral T1 hypointense lesions are positively correlated with the disability of multiple sclerosis (MS) patients. Hence, they could be used as an objective marker for evaluating the progression of the disease. Up to this date, there has not been a system...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981477/ https://www.ncbi.nlm.nih.gov/pubmed/35218155 http://dx.doi.org/10.1111/cns.13815 |
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author | Valizadeh, Amir Fattahi, Mohammad Reza Sadeghi, Maryam Saghab Torbati, Mehrnush Sahraian, Mohammad Ali Azimi, Amir Reza |
author_facet | Valizadeh, Amir Fattahi, Mohammad Reza Sadeghi, Maryam Saghab Torbati, Mehrnush Sahraian, Mohammad Ali Azimi, Amir Reza |
author_sort | Valizadeh, Amir |
collection | PubMed |
description | BACKGROUND: Previous research has shown that cerebral T1 hypointense lesions are positively correlated with the disability of multiple sclerosis (MS) patients. Hence, they could be used as an objective marker for evaluating the progression of the disease. Up to this date, there has not been a systematic evaluation of the effects of disease‐modifying therapies (DMTs) on this prognostic marker. OBJECTIVES: To evaluate the effects of FDA‐approved DMTs on the numbers and volume of T1 hypointense lesions in adult patients with MS. METHODS: We included studies with the mentioned desired outcomes. In March 2021, we searched MEDLINE (Ovid), Embase, and CENTRAL to find relevant studies. All included studies were assessed for the risk of bias using the RoB‐2 tool. Extracted data were analyzed using a random‐effects model. Certainty of evidence was assessed using GRADE. RESULTS: Thirteen studies with 7484 participants were included. Meta‐analysis revealed the mean difference between the intervention and comparator groups for the number of lesions was −1.3 (95% CI: −2.1, −0.5) and for the mean volume of lesions was −363.1 (95% CI: −611.6, −114.6). Certainty of evidence was judged to be moderate. Heterogeneity was considerable. DISCUSSION: DMTs reduce the number and volume of T1 hypointense lesions. Although, these findings must be interpreted cautiously due to the high values of heterogeneity. |
format | Online Article Text |
id | pubmed-8981477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89814772022-04-11 Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis Valizadeh, Amir Fattahi, Mohammad Reza Sadeghi, Maryam Saghab Torbati, Mehrnush Sahraian, Mohammad Ali Azimi, Amir Reza CNS Neurosci Ther Meta‐analysis BACKGROUND: Previous research has shown that cerebral T1 hypointense lesions are positively correlated with the disability of multiple sclerosis (MS) patients. Hence, they could be used as an objective marker for evaluating the progression of the disease. Up to this date, there has not been a systematic evaluation of the effects of disease‐modifying therapies (DMTs) on this prognostic marker. OBJECTIVES: To evaluate the effects of FDA‐approved DMTs on the numbers and volume of T1 hypointense lesions in adult patients with MS. METHODS: We included studies with the mentioned desired outcomes. In March 2021, we searched MEDLINE (Ovid), Embase, and CENTRAL to find relevant studies. All included studies were assessed for the risk of bias using the RoB‐2 tool. Extracted data were analyzed using a random‐effects model. Certainty of evidence was assessed using GRADE. RESULTS: Thirteen studies with 7484 participants were included. Meta‐analysis revealed the mean difference between the intervention and comparator groups for the number of lesions was −1.3 (95% CI: −2.1, −0.5) and for the mean volume of lesions was −363.1 (95% CI: −611.6, −114.6). Certainty of evidence was judged to be moderate. Heterogeneity was considerable. DISCUSSION: DMTs reduce the number and volume of T1 hypointense lesions. Although, these findings must be interpreted cautiously due to the high values of heterogeneity. John Wiley and Sons Inc. 2022-02-25 /pmc/articles/PMC8981477/ /pubmed/35218155 http://dx.doi.org/10.1111/cns.13815 Text en © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Meta‐analysis Valizadeh, Amir Fattahi, Mohammad Reza Sadeghi, Maryam Saghab Torbati, Mehrnush Sahraian, Mohammad Ali Azimi, Amir Reza Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis |
title | Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis |
title_full | Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis |
title_fullStr | Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis |
title_full_unstemmed | Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis |
title_short | Disease‐modifying therapies and T1 hypointense lesions in patients with multiple sclerosis: A systematic review and meta‐analysis |
title_sort | disease‐modifying therapies and t1 hypointense lesions in patients with multiple sclerosis: a systematic review and meta‐analysis |
topic | Meta‐analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981477/ https://www.ncbi.nlm.nih.gov/pubmed/35218155 http://dx.doi.org/10.1111/cns.13815 |
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