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Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients()
BACKGROUND AND OBJECTIVES: While the literature supports the idea that multiple sclerosis (MS) and migraine are related, the exact mechanism(s) of this association is not well understood. Observations of increased contrast enhancing (CE) lesion activity in individual MS patients suffering from migra...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552815/ https://www.ncbi.nlm.nih.gov/pubmed/26448911 http://dx.doi.org/10.1016/j.nicl.2015.07.013 |
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author | Graziano, Elliot Hagemeier, Jesper Weinstock-Guttman, Bianca Ramasamy, Deepa P. Zivadinov, Robert |
author_facet | Graziano, Elliot Hagemeier, Jesper Weinstock-Guttman, Bianca Ramasamy, Deepa P. Zivadinov, Robert |
author_sort | Graziano, Elliot |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: While the literature supports the idea that multiple sclerosis (MS) and migraine are related, the exact mechanism(s) of this association is not well understood. Observations of increased contrast enhancing (CE) lesion activity in individual MS patients suffering from migraine prompted us to determine a relationship between migraine and MRI outcomes in a large cohort of MS patients. METHODS: We included 509 MS and 64 clinically isolated syndrome (CIS) patients and 251 age- and sex-matched healthy individuals (HIs) who obtained 3 T MRI and were assessed for history of migraine. Number and volume of T2, T1 and CE lesions and brain volume measures were determined. The MRI findings were analyzed adjusting for key covariates and correcting for multiple comparisons. RESULTS: More MS (22.2%) and CIS (17.2%) patients had migraine, compared to HIs (14.6%, p = 0.067). More MS patients with migraine presented with CE lesions compared to those without (35.4% vs. 23.7%, p = 0.013). MS migraine patients had significantly increased number (p = 0.019) and volume (p = 0.022) of CE lesions compared to those without. In the regression analysis, MS migraine patients had an increased number of CE lesions (B = 1.242, p = 0.001), specifically those with relapsing–remitting disease course (B = 1.377, p = 0.001). No significant association of other MRI measures and migraine was found in MS and CIS patients or in HIs. CONCLUSIONS: Our findings suggest an increased inflammatory pathobiology in MS patients with migraine headaches requiring possibly more frequent MRIs and also more efficient anti-inflammatory treatment. |
format | Online Article Text |
id | pubmed-4552815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-45528152015-10-07 Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() Graziano, Elliot Hagemeier, Jesper Weinstock-Guttman, Bianca Ramasamy, Deepa P. Zivadinov, Robert Neuroimage Clin Regular Article BACKGROUND AND OBJECTIVES: While the literature supports the idea that multiple sclerosis (MS) and migraine are related, the exact mechanism(s) of this association is not well understood. Observations of increased contrast enhancing (CE) lesion activity in individual MS patients suffering from migraine prompted us to determine a relationship between migraine and MRI outcomes in a large cohort of MS patients. METHODS: We included 509 MS and 64 clinically isolated syndrome (CIS) patients and 251 age- and sex-matched healthy individuals (HIs) who obtained 3 T MRI and were assessed for history of migraine. Number and volume of T2, T1 and CE lesions and brain volume measures were determined. The MRI findings were analyzed adjusting for key covariates and correcting for multiple comparisons. RESULTS: More MS (22.2%) and CIS (17.2%) patients had migraine, compared to HIs (14.6%, p = 0.067). More MS patients with migraine presented with CE lesions compared to those without (35.4% vs. 23.7%, p = 0.013). MS migraine patients had significantly increased number (p = 0.019) and volume (p = 0.022) of CE lesions compared to those without. In the regression analysis, MS migraine patients had an increased number of CE lesions (B = 1.242, p = 0.001), specifically those with relapsing–remitting disease course (B = 1.377, p = 0.001). No significant association of other MRI measures and migraine was found in MS and CIS patients or in HIs. CONCLUSIONS: Our findings suggest an increased inflammatory pathobiology in MS patients with migraine headaches requiring possibly more frequent MRIs and also more efficient anti-inflammatory treatment. Elsevier 2015-08-01 /pmc/articles/PMC4552815/ /pubmed/26448911 http://dx.doi.org/10.1016/j.nicl.2015.07.013 Text en © 2015 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Graziano, Elliot Hagemeier, Jesper Weinstock-Guttman, Bianca Ramasamy, Deepa P. Zivadinov, Robert Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() |
title | Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() |
title_full | Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() |
title_fullStr | Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() |
title_full_unstemmed | Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() |
title_short | Increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() |
title_sort | increased contrast enhancing lesion activity in relapsing–remitting multiple sclerosis migraine patients() |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552815/ https://www.ncbi.nlm.nih.gov/pubmed/26448911 http://dx.doi.org/10.1016/j.nicl.2015.07.013 |
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