Cargando…
A neuropathologic feature of brain aging: multi-lumen vascular profiles
Cerebrovascular pathologies other than frank infarctions are commonly seen in aged brains. Here, we focus on multi-lumen vascular profiles (MVPs), which are characterized by multiple vessel lumens enclosed in a single vascular channel. Little information exists on the prevalence, risk factors, and c...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464008/ https://www.ncbi.nlm.nih.gov/pubmed/37641147 http://dx.doi.org/10.1186/s40478-023-01638-2 |
_version_ | 1785098366986747904 |
---|---|
author | Ighodaro, Eseosa T. Shahidehpour, Ryan K. Bachstetter, Adam D. Abner, Erin L. Nelson, Ruth S. Fardo, David W. Shih, Andy Y. Grant, Roger I. Neltner, Janna H. Schmitt, Frederick A. Jicha, Gregory A. Kryscio, Richard J. Wilcock, Donna M. Van Eldik, Linda J. Nelson, Peter T. |
author_facet | Ighodaro, Eseosa T. Shahidehpour, Ryan K. Bachstetter, Adam D. Abner, Erin L. Nelson, Ruth S. Fardo, David W. Shih, Andy Y. Grant, Roger I. Neltner, Janna H. Schmitt, Frederick A. Jicha, Gregory A. Kryscio, Richard J. Wilcock, Donna M. Van Eldik, Linda J. Nelson, Peter T. |
author_sort | Ighodaro, Eseosa T. |
collection | PubMed |
description | Cerebrovascular pathologies other than frank infarctions are commonly seen in aged brains. Here, we focus on multi-lumen vascular profiles (MVPs), which are characterized by multiple vessel lumens enclosed in a single vascular channel. Little information exists on the prevalence, risk factors, and co-pathologies of MVPs. Therefore, we used samples and data from the University of Kentucky Alzheimer’s Disease Research Center (n = 91), the University of Kentucky Pathology Department (n = 31), and the University of Pittsburgh Pathology Department (n = 4) to study MVPs. Age at death was correlated with MVP density in the frontal neocortex, Brodmann Area 9 (r = 0.51; p < 0.0001). Exploratory analyses were performed to evaluate the association between conventional vascular risk factors (e.g., hypertension, diabetes), cardiovascular diseases (e.g., heart attack, arrhythmia), and cerebrovascular disease (e.g., stroke); the only nominal association with MVP density was a self-reported history of brain trauma (Prevalence Ratio = 2.1; 95 CI 1.1–3.9, before correcting for multiple comparisons). No specific associations were detected between neuropathological (e.g., brain arteriolosclerosis) or genetic (e.g., APOE) variables and MVP density. Using a tissue clearing method called SeeDB, we provide 3-dimensional images of MVPs in brain tissue. We conclude that MVPs are an age-related brain pathology and more work is required to identify their clinical-pathological correlation and associated risk factors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01638-2. |
format | Online Article Text |
id | pubmed-10464008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104640082023-08-30 A neuropathologic feature of brain aging: multi-lumen vascular profiles Ighodaro, Eseosa T. Shahidehpour, Ryan K. Bachstetter, Adam D. Abner, Erin L. Nelson, Ruth S. Fardo, David W. Shih, Andy Y. Grant, Roger I. Neltner, Janna H. Schmitt, Frederick A. Jicha, Gregory A. Kryscio, Richard J. Wilcock, Donna M. Van Eldik, Linda J. Nelson, Peter T. Acta Neuropathol Commun Research Cerebrovascular pathologies other than frank infarctions are commonly seen in aged brains. Here, we focus on multi-lumen vascular profiles (MVPs), which are characterized by multiple vessel lumens enclosed in a single vascular channel. Little information exists on the prevalence, risk factors, and co-pathologies of MVPs. Therefore, we used samples and data from the University of Kentucky Alzheimer’s Disease Research Center (n = 91), the University of Kentucky Pathology Department (n = 31), and the University of Pittsburgh Pathology Department (n = 4) to study MVPs. Age at death was correlated with MVP density in the frontal neocortex, Brodmann Area 9 (r = 0.51; p < 0.0001). Exploratory analyses were performed to evaluate the association between conventional vascular risk factors (e.g., hypertension, diabetes), cardiovascular diseases (e.g., heart attack, arrhythmia), and cerebrovascular disease (e.g., stroke); the only nominal association with MVP density was a self-reported history of brain trauma (Prevalence Ratio = 2.1; 95 CI 1.1–3.9, before correcting for multiple comparisons). No specific associations were detected between neuropathological (e.g., brain arteriolosclerosis) or genetic (e.g., APOE) variables and MVP density. Using a tissue clearing method called SeeDB, we provide 3-dimensional images of MVPs in brain tissue. We conclude that MVPs are an age-related brain pathology and more work is required to identify their clinical-pathological correlation and associated risk factors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-023-01638-2. BioMed Central 2023-08-28 /pmc/articles/PMC10464008/ /pubmed/37641147 http://dx.doi.org/10.1186/s40478-023-01638-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Ighodaro, Eseosa T. Shahidehpour, Ryan K. Bachstetter, Adam D. Abner, Erin L. Nelson, Ruth S. Fardo, David W. Shih, Andy Y. Grant, Roger I. Neltner, Janna H. Schmitt, Frederick A. Jicha, Gregory A. Kryscio, Richard J. Wilcock, Donna M. Van Eldik, Linda J. Nelson, Peter T. A neuropathologic feature of brain aging: multi-lumen vascular profiles |
title | A neuropathologic feature of brain aging: multi-lumen vascular profiles |
title_full | A neuropathologic feature of brain aging: multi-lumen vascular profiles |
title_fullStr | A neuropathologic feature of brain aging: multi-lumen vascular profiles |
title_full_unstemmed | A neuropathologic feature of brain aging: multi-lumen vascular profiles |
title_short | A neuropathologic feature of brain aging: multi-lumen vascular profiles |
title_sort | neuropathologic feature of brain aging: multi-lumen vascular profiles |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464008/ https://www.ncbi.nlm.nih.gov/pubmed/37641147 http://dx.doi.org/10.1186/s40478-023-01638-2 |
work_keys_str_mv | AT ighodaroeseosat aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT shahidehpourryank aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT bachstetteradamd aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT abnererinl aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT nelsonruths aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT fardodavidw aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT shihandyy aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT grantrogeri aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT neltnerjannah aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT schmittfredericka aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT jichagregorya aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT krysciorichardj aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT wilcockdonnam aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT vaneldiklindaj aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT nelsonpetert aneuropathologicfeatureofbrainagingmultilumenvascularprofiles AT ighodaroeseosat neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT shahidehpourryank neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT bachstetteradamd neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT abnererinl neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT nelsonruths neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT fardodavidw neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT shihandyy neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT grantrogeri neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT neltnerjannah neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT schmittfredericka neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT jichagregorya neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT krysciorichardj neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT wilcockdonnam neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT vaneldiklindaj neuropathologicfeatureofbrainagingmultilumenvascularprofiles AT nelsonpetert neuropathologicfeatureofbrainagingmultilumenvascularprofiles |