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Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression
(1) Background: Multiple sclerosis (MS) is an auto-immune, chronic, neuroinflammatory, demyelinating disease that affects mainly young patients. This progressive inflammatory process causes the chronic loss of brain tissue and results in a deterioration in quality of life. To monitor neuroinflammato...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453931/ https://www.ncbi.nlm.nih.gov/pubmed/37627928 http://dx.doi.org/10.3390/diagnostics13162668 |
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author | Jankowska, Anna Chwojnicki, Kamil Grzywińska, Małgorzata Trzonkowski, Piotr Szurowska, Edyta |
author_facet | Jankowska, Anna Chwojnicki, Kamil Grzywińska, Małgorzata Trzonkowski, Piotr Szurowska, Edyta |
author_sort | Jankowska, Anna |
collection | PubMed |
description | (1) Background: Multiple sclerosis (MS) is an auto-immune, chronic, neuroinflammatory, demyelinating disease that affects mainly young patients. This progressive inflammatory process causes the chronic loss of brain tissue and results in a deterioration in quality of life. To monitor neuroinflammatory process activity and predict the further development of disease, it is necessary to find a suitable biomarker that could easily be used. In this research, we verify the usability of choroid plexus (CP) volume, a new MS biomarker, in the monitoring of the progression of multiple sclerosis disease. (2) Methods: A single-center, prospective study with three groups of patients was conducted based on the following groups: MS patients who received experimental cellular therapy (Treg), treatment-naïve MS patients and healthy controls. (3) Results: This study concludes that there is a correlation between the CPV/TIV (choroid plexus/total intracranial volume) ratio and the progress of multiple sclerosis disease—patients with MS (MS + Treg) had larger volumes of choroid plexuses. CPV/TIV ratios in MS groups were constantly and significantly growing. In the Treg group, patients with relapses had larger plexuses in comparison to the group with no relapses of MS. A similar correlation was observed for the GD+ group (patients with postcontrast enhancing plaques) compared against the non-GD group (patients without postcontrast enhancing plaques). (4) Conclusion: Choroid plexus volume, due to its immunological function, correlates with the inflammatory process in the central nervous system. We consider it to become a valuable radiological biomarker of MS activity. |
format | Online Article Text |
id | pubmed-10453931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104539312023-08-26 Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression Jankowska, Anna Chwojnicki, Kamil Grzywińska, Małgorzata Trzonkowski, Piotr Szurowska, Edyta Diagnostics (Basel) Article (1) Background: Multiple sclerosis (MS) is an auto-immune, chronic, neuroinflammatory, demyelinating disease that affects mainly young patients. This progressive inflammatory process causes the chronic loss of brain tissue and results in a deterioration in quality of life. To monitor neuroinflammatory process activity and predict the further development of disease, it is necessary to find a suitable biomarker that could easily be used. In this research, we verify the usability of choroid plexus (CP) volume, a new MS biomarker, in the monitoring of the progression of multiple sclerosis disease. (2) Methods: A single-center, prospective study with three groups of patients was conducted based on the following groups: MS patients who received experimental cellular therapy (Treg), treatment-naïve MS patients and healthy controls. (3) Results: This study concludes that there is a correlation between the CPV/TIV (choroid plexus/total intracranial volume) ratio and the progress of multiple sclerosis disease—patients with MS (MS + Treg) had larger volumes of choroid plexuses. CPV/TIV ratios in MS groups were constantly and significantly growing. In the Treg group, patients with relapses had larger plexuses in comparison to the group with no relapses of MS. A similar correlation was observed for the GD+ group (patients with postcontrast enhancing plaques) compared against the non-GD group (patients without postcontrast enhancing plaques). (4) Conclusion: Choroid plexus volume, due to its immunological function, correlates with the inflammatory process in the central nervous system. We consider it to become a valuable radiological biomarker of MS activity. MDPI 2023-08-14 /pmc/articles/PMC10453931/ /pubmed/37627928 http://dx.doi.org/10.3390/diagnostics13162668 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jankowska, Anna Chwojnicki, Kamil Grzywińska, Małgorzata Trzonkowski, Piotr Szurowska, Edyta Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression |
title | Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression |
title_full | Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression |
title_fullStr | Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression |
title_full_unstemmed | Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression |
title_short | Choroid Plexus Volume Change—A Candidate for a New Radiological Marker of MS Progression |
title_sort | choroid plexus volume change—a candidate for a new radiological marker of ms progression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453931/ https://www.ncbi.nlm.nih.gov/pubmed/37627928 http://dx.doi.org/10.3390/diagnostics13162668 |
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