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Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study
BACKGROUND: Cerebral microbleeds (MBs) are understood as an important radiologic marker of intracerebral hemorrhage. We sought to investigate the temporal changes of MBs and clinical factors associated with the changes using long-term follow-up MRI. METHODS/PRINCIPAL FINDINGS: From October 2002 to J...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191164/ https://www.ncbi.nlm.nih.gov/pubmed/22022473 http://dx.doi.org/10.1371/journal.pone.0025930 |
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author | Lee, Seung-Hoon Lee, Soon-Tae Kim, Beom Joon Park, Hee-Kwon Kim, Chi-Kyung Jung, Keun-Hwa Roh, Jae-Kyu |
author_facet | Lee, Seung-Hoon Lee, Soon-Tae Kim, Beom Joon Park, Hee-Kwon Kim, Chi-Kyung Jung, Keun-Hwa Roh, Jae-Kyu |
author_sort | Lee, Seung-Hoon |
collection | PubMed |
description | BACKGROUND: Cerebral microbleeds (MBs) are understood as an important radiologic marker of intracerebral hemorrhage. We sought to investigate the temporal changes of MBs and clinical factors associated with the changes using long-term follow-up MRI. METHODS/PRINCIPAL FINDINGS: From October 2002 to July 2006, we prospectively enrolled patients with stroke or transient ischemic attack, and followed-up their brain MRIs with an interval >12 mo. We compared demographic factors, vascular risk factors, laboratory findings, and radiologic factors according to the presence or changes of MBs. A total of 224 patients successfully completed the follow-up examinations (mean, 27 months). Newly developed MBs were noted in 10 patients (6.8%) among those without MBs at baseline (n = 148), and in those with MBs at baseline (n = 76), the MB count had decreased in 11 patients (14.5%), and increased in 41 patients (53.9%). The estimated annual rate of change of MB numbers was 0.80 lesions per year in all patients, a value which became greater in those patients who exhibited MBs at baseline (MBs≥5, 5.43 lesions per year). Strokes due to small vessel occlusion and intracerebral hemorrhage, as well as white matter lesions were independently associated with an increased MB count, whereas the highest quartile of low-density lipoprotein (LDL) cholesterol was associated with a decreased MB count. CONCLUSION: During the follow-up period, most of MBs showed dynamic temporal change. Symptomatic or asymptomatic small vessel diseases appear to act as risk factors while in contrast, a high level of LDL cholesterol may act as a protective factor against MB increase. |
format | Online Article Text |
id | pubmed-3191164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31911642011-10-21 Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study Lee, Seung-Hoon Lee, Soon-Tae Kim, Beom Joon Park, Hee-Kwon Kim, Chi-Kyung Jung, Keun-Hwa Roh, Jae-Kyu PLoS One Research Article BACKGROUND: Cerebral microbleeds (MBs) are understood as an important radiologic marker of intracerebral hemorrhage. We sought to investigate the temporal changes of MBs and clinical factors associated with the changes using long-term follow-up MRI. METHODS/PRINCIPAL FINDINGS: From October 2002 to July 2006, we prospectively enrolled patients with stroke or transient ischemic attack, and followed-up their brain MRIs with an interval >12 mo. We compared demographic factors, vascular risk factors, laboratory findings, and radiologic factors according to the presence or changes of MBs. A total of 224 patients successfully completed the follow-up examinations (mean, 27 months). Newly developed MBs were noted in 10 patients (6.8%) among those without MBs at baseline (n = 148), and in those with MBs at baseline (n = 76), the MB count had decreased in 11 patients (14.5%), and increased in 41 patients (53.9%). The estimated annual rate of change of MB numbers was 0.80 lesions per year in all patients, a value which became greater in those patients who exhibited MBs at baseline (MBs≥5, 5.43 lesions per year). Strokes due to small vessel occlusion and intracerebral hemorrhage, as well as white matter lesions were independently associated with an increased MB count, whereas the highest quartile of low-density lipoprotein (LDL) cholesterol was associated with a decreased MB count. CONCLUSION: During the follow-up period, most of MBs showed dynamic temporal change. Symptomatic or asymptomatic small vessel diseases appear to act as risk factors while in contrast, a high level of LDL cholesterol may act as a protective factor against MB increase. Public Library of Science 2011-10-11 /pmc/articles/PMC3191164/ /pubmed/22022473 http://dx.doi.org/10.1371/journal.pone.0025930 Text en Lee et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lee, Seung-Hoon Lee, Soon-Tae Kim, Beom Joon Park, Hee-Kwon Kim, Chi-Kyung Jung, Keun-Hwa Roh, Jae-Kyu Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study |
title | Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study |
title_full | Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study |
title_fullStr | Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study |
title_full_unstemmed | Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study |
title_short | Dynamic Temporal Change of Cerebral Microbleeds: Long-Term Follow-Up MRI Study |
title_sort | dynamic temporal change of cerebral microbleeds: long-term follow-up mri study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191164/ https://www.ncbi.nlm.nih.gov/pubmed/22022473 http://dx.doi.org/10.1371/journal.pone.0025930 |
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