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Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis
BACKGROUND AND PURPOSE: We have commonly observed prominent cerebral veins on susceptibility‐weighted angiography (SWAN) in acute meningoencephalitis. This study aimed to investigate the clinical significance of these findings. METHODS: Cerebral veins on SWAN of 98 patients with acute meningoencepha...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636387/ https://www.ncbi.nlm.nih.gov/pubmed/37721542 http://dx.doi.org/10.1002/brb3.3255 |
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author | Jung, Yo Han Park, Mina Joo, Bio Suh, Sang Hyun Lee, Kyung‐Yul Ahn, Sung Jun |
author_facet | Jung, Yo Han Park, Mina Joo, Bio Suh, Sang Hyun Lee, Kyung‐Yul Ahn, Sung Jun |
author_sort | Jung, Yo Han |
collection | PubMed |
description | BACKGROUND AND PURPOSE: We have commonly observed prominent cerebral veins on susceptibility‐weighted angiography (SWAN) in acute meningoencephalitis. This study aimed to investigate the clinical significance of these findings. METHODS: Cerebral veins on SWAN of 98 patients with acute meningoencephalitis diagnosed from February 2016 through October 2020 were classified into three groups according to the degree of venous prominence (mild, 23; moderate, 53; and prominent, 22). Clinical variables and laboratory findings were compared between these groups. The influence of variables on the prediction of prominent cerebral veins was measured by random forest (RF) and gradient boosting machine (GBM). RESULTS: As cerebral veins became more prominent, cerebrospinal fluid (CSF) glucose level decreased (69.61 ± 29.05 vs. 59.72 ± 22.57 vs. 48.36 ± 20.29 mg/dL, p = .01) and CSF protein level increased (100.73 ± 82.98 vs. 104.73 ± 70.99 vs. 159.12 ± 118.15 mg/dL, p = .03). The etiology of meningoencephalitis, neurological symptoms, and increased intracranial pressure (ICP) signs differed between groups (p < .05). RF and GBM demonstrated that CSF protein level was the variable with the highest power to predict the prominent cerebral vein (mean decrease in node impurity: 4.19, relative influence: 50.66). CONCLUSION: The presence of prominent cerebral veins on SWAN in acute meningoencephalitis was significantly associated with a low CSF glucose level and a high CSF protein level, as well as ICP. Thus, the visual grade of the cerebral veins on SWAN may be utilized for the management of patients with acute meningoencephalitis. |
format | Online Article Text |
id | pubmed-10636387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106363872023-11-15 Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis Jung, Yo Han Park, Mina Joo, Bio Suh, Sang Hyun Lee, Kyung‐Yul Ahn, Sung Jun Brain Behav Original Articles BACKGROUND AND PURPOSE: We have commonly observed prominent cerebral veins on susceptibility‐weighted angiography (SWAN) in acute meningoencephalitis. This study aimed to investigate the clinical significance of these findings. METHODS: Cerebral veins on SWAN of 98 patients with acute meningoencephalitis diagnosed from February 2016 through October 2020 were classified into three groups according to the degree of venous prominence (mild, 23; moderate, 53; and prominent, 22). Clinical variables and laboratory findings were compared between these groups. The influence of variables on the prediction of prominent cerebral veins was measured by random forest (RF) and gradient boosting machine (GBM). RESULTS: As cerebral veins became more prominent, cerebrospinal fluid (CSF) glucose level decreased (69.61 ± 29.05 vs. 59.72 ± 22.57 vs. 48.36 ± 20.29 mg/dL, p = .01) and CSF protein level increased (100.73 ± 82.98 vs. 104.73 ± 70.99 vs. 159.12 ± 118.15 mg/dL, p = .03). The etiology of meningoencephalitis, neurological symptoms, and increased intracranial pressure (ICP) signs differed between groups (p < .05). RF and GBM demonstrated that CSF protein level was the variable with the highest power to predict the prominent cerebral vein (mean decrease in node impurity: 4.19, relative influence: 50.66). CONCLUSION: The presence of prominent cerebral veins on SWAN in acute meningoencephalitis was significantly associated with a low CSF glucose level and a high CSF protein level, as well as ICP. Thus, the visual grade of the cerebral veins on SWAN may be utilized for the management of patients with acute meningoencephalitis. John Wiley and Sons Inc. 2023-09-18 /pmc/articles/PMC10636387/ /pubmed/37721542 http://dx.doi.org/10.1002/brb3.3255 Text en © 2023 The Authors. Brain and Behavior published by Wiley Periodicals LLC. 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 | Original Articles Jung, Yo Han Park, Mina Joo, Bio Suh, Sang Hyun Lee, Kyung‐Yul Ahn, Sung Jun Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis |
title | Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis |
title_full | Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis |
title_fullStr | Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis |
title_full_unstemmed | Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis |
title_short | Prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis |
title_sort | prominent cerebral veins on susceptibility‐weighted angiography in acute meningoencephalitis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10636387/ https://www.ncbi.nlm.nih.gov/pubmed/37721542 http://dx.doi.org/10.1002/brb3.3255 |
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