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Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations
Cerebral microbleeds (microbleeds) are small, punctuate hypointense lesions seen in T2* Gradient-Recall Echo (GRE) and Susceptibility-Weighted (SWI) Magnetic Resonance Imaging (MRI) sequences, corresponding to areas of hemosiderin breakdown products from prior microscopic hemorrhages. They occur in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881231/ https://www.ncbi.nlm.nih.gov/pubmed/24432010 http://dx.doi.org/10.3389/fneur.2013.00205 |
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author | Yates, Paul A. Villemagne, Victor L. Ellis, Kathryn A. Desmond, Patricia M. Masters, Colin L. Rowe, Christopher C. |
author_facet | Yates, Paul A. Villemagne, Victor L. Ellis, Kathryn A. Desmond, Patricia M. Masters, Colin L. Rowe, Christopher C. |
author_sort | Yates, Paul A. |
collection | PubMed |
description | Cerebral microbleeds (microbleeds) are small, punctuate hypointense lesions seen in T2* Gradient-Recall Echo (GRE) and Susceptibility-Weighted (SWI) Magnetic Resonance Imaging (MRI) sequences, corresponding to areas of hemosiderin breakdown products from prior microscopic hemorrhages. They occur in the setting of impaired small vessel integrity, commonly due to either hypertensive vasculopathy or cerebral amyloid angiopathy. Microbleeds are more prevalent in individuals with Alzheimer’s disease (AD) dementia and in those with both ischemic and hemorrhagic stroke. However they are also found in asymptomatic individuals, with increasing prevalence with age, particularly in carriers of the Apolipoprotein (APOE) ε4 allele. Other neuroimaging findings that have been linked with microbleeds include lacunar infarcts and white matter hyperintensities on MRI, and increased cerebral β-amyloid burden using (11)C-PiB Positron Emission Tomography. The presence of microbleeds has been suggested to confer increased risk of incident intracerebral hemorrhage – particularly in the setting of anticoagulation – and of complications of immunotherapy for AD. Prospective data regarding the natural history and sequelae of microbleeds are currently limited, however there is a growing evidence base that will serve to inform clinical decision-making in the future. |
format | Online Article Text |
id | pubmed-3881231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38812312014-01-15 Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations Yates, Paul A. Villemagne, Victor L. Ellis, Kathryn A. Desmond, Patricia M. Masters, Colin L. Rowe, Christopher C. Front Neurol Neuroscience Cerebral microbleeds (microbleeds) are small, punctuate hypointense lesions seen in T2* Gradient-Recall Echo (GRE) and Susceptibility-Weighted (SWI) Magnetic Resonance Imaging (MRI) sequences, corresponding to areas of hemosiderin breakdown products from prior microscopic hemorrhages. They occur in the setting of impaired small vessel integrity, commonly due to either hypertensive vasculopathy or cerebral amyloid angiopathy. Microbleeds are more prevalent in individuals with Alzheimer’s disease (AD) dementia and in those with both ischemic and hemorrhagic stroke. However they are also found in asymptomatic individuals, with increasing prevalence with age, particularly in carriers of the Apolipoprotein (APOE) ε4 allele. Other neuroimaging findings that have been linked with microbleeds include lacunar infarcts and white matter hyperintensities on MRI, and increased cerebral β-amyloid burden using (11)C-PiB Positron Emission Tomography. The presence of microbleeds has been suggested to confer increased risk of incident intracerebral hemorrhage – particularly in the setting of anticoagulation – and of complications of immunotherapy for AD. Prospective data regarding the natural history and sequelae of microbleeds are currently limited, however there is a growing evidence base that will serve to inform clinical decision-making in the future. Frontiers Media S.A. 2014-01-06 /pmc/articles/PMC3881231/ /pubmed/24432010 http://dx.doi.org/10.3389/fneur.2013.00205 Text en Copyright © 2014 Yates, Villemagne, Ellis, Desmond, Masters and Rowe. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Yates, Paul A. Villemagne, Victor L. Ellis, Kathryn A. Desmond, Patricia M. Masters, Colin L. Rowe, Christopher C. Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations |
title | Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations |
title_full | Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations |
title_fullStr | Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations |
title_full_unstemmed | Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations |
title_short | Cerebral Microbleeds: A Review of Clinical, Genetic, and Neuroimaging Associations |
title_sort | cerebral microbleeds: a review of clinical, genetic, and neuroimaging associations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881231/ https://www.ncbi.nlm.nih.gov/pubmed/24432010 http://dx.doi.org/10.3389/fneur.2013.00205 |
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