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Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus

To determine whether any brain MR abnormalities, including enlarged perivascular spaces (EPVS), were associated with disease activity in systemic lupus erythematosus (SLE) as an inflammatory activity. One hundred and thirty SLE patients with normal MR findings were assessed. With regard to MRI abnor...

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Autores principales: Miyata, Mari, Kakeda, Shingo, Iwata, Shigeru, Nakayamada, Shingo, Ide, Satoru, Watanabe, Keita, Moriya, Junji, Tanaka, Yoshiya, Korogi, Yukunori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626765/
https://www.ncbi.nlm.nih.gov/pubmed/28974720
http://dx.doi.org/10.1038/s41598-017-12966-4
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author Miyata, Mari
Kakeda, Shingo
Iwata, Shigeru
Nakayamada, Shingo
Ide, Satoru
Watanabe, Keita
Moriya, Junji
Tanaka, Yoshiya
Korogi, Yukunori
author_facet Miyata, Mari
Kakeda, Shingo
Iwata, Shigeru
Nakayamada, Shingo
Ide, Satoru
Watanabe, Keita
Moriya, Junji
Tanaka, Yoshiya
Korogi, Yukunori
author_sort Miyata, Mari
collection PubMed
description To determine whether any brain MR abnormalities, including enlarged perivascular spaces (EPVS), were associated with disease activity in systemic lupus erythematosus (SLE) as an inflammatory activity. One hundred and thirty SLE patients with normal MR findings were assessed. With regard to MRI abnormalities, patients with brain atrophy and mild white matter hyperintensity (WMH) on T2WI were not excluded. The disease activity was assessed using the SLEDAI and the BILAG scores. The imaging characteristics included centrum semiovale EPVS (CS- EPVS) and basal ganglia EPVS on T2WI, WMH, and brain atrophy. We used univariate and multivariate logistic regression analyses to determine the clinical (vascular risk factors and blood examinations) and imaging characteristics that were associated with the disease activity of SLE. High CS-EPVS to be the only factor that was independently associated with the severity of the SLEDAI and BILAG scores (odds ratio [OR] 5.77; 95% confidence interval [CI] 2.21–15.00; p < 0.001 for the SLEDAI, and OR 2.64; 95% CI 1.03–6.74; p = 0.042 for the BILAG score). The CS-EPVS in the SLE patients are associated with the systemic disease activity, suggesting that CS- EPVS may be indicative of the reactive changes of the white matter due to the inflammatory activity.
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spelling pubmed-56267652017-10-12 Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus Miyata, Mari Kakeda, Shingo Iwata, Shigeru Nakayamada, Shingo Ide, Satoru Watanabe, Keita Moriya, Junji Tanaka, Yoshiya Korogi, Yukunori Sci Rep Article To determine whether any brain MR abnormalities, including enlarged perivascular spaces (EPVS), were associated with disease activity in systemic lupus erythematosus (SLE) as an inflammatory activity. One hundred and thirty SLE patients with normal MR findings were assessed. With regard to MRI abnormalities, patients with brain atrophy and mild white matter hyperintensity (WMH) on T2WI were not excluded. The disease activity was assessed using the SLEDAI and the BILAG scores. The imaging characteristics included centrum semiovale EPVS (CS- EPVS) and basal ganglia EPVS on T2WI, WMH, and brain atrophy. We used univariate and multivariate logistic regression analyses to determine the clinical (vascular risk factors and blood examinations) and imaging characteristics that were associated with the disease activity of SLE. High CS-EPVS to be the only factor that was independently associated with the severity of the SLEDAI and BILAG scores (odds ratio [OR] 5.77; 95% confidence interval [CI] 2.21–15.00; p < 0.001 for the SLEDAI, and OR 2.64; 95% CI 1.03–6.74; p = 0.042 for the BILAG score). The CS-EPVS in the SLE patients are associated with the systemic disease activity, suggesting that CS- EPVS may be indicative of the reactive changes of the white matter due to the inflammatory activity. Nature Publishing Group UK 2017-10-03 /pmc/articles/PMC5626765/ /pubmed/28974720 http://dx.doi.org/10.1038/s41598-017-12966-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Miyata, Mari
Kakeda, Shingo
Iwata, Shigeru
Nakayamada, Shingo
Ide, Satoru
Watanabe, Keita
Moriya, Junji
Tanaka, Yoshiya
Korogi, Yukunori
Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus
title Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus
title_full Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus
title_fullStr Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus
title_full_unstemmed Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus
title_short Enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus
title_sort enlarged perivascular spaces are associated with the disease activity in systemic lupus erythematosus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626765/
https://www.ncbi.nlm.nih.gov/pubmed/28974720
http://dx.doi.org/10.1038/s41598-017-12966-4
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