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Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm
BACKGROUND: Fragmentation of the tunica media is a hallmark of intracranial aneurysm formation, often leading to aneurysmal progression and subsequent rupture. The objective of this study is to determine the plasma level of elastin fragments in the lumen of ruptured versus unruptured human intracran...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201439/ https://www.ncbi.nlm.nih.gov/pubmed/30371156 http://dx.doi.org/10.1161/JAHA.118.010051 |
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author | Nakagawa, Daichi Zanaty, Mario Hudson, Joseph Teferi, Nahom Ishii, Daizo Allan, Lauren Jabbour, Pascal Ortega‐Gutierrez, Santiago Samaniego, Edgar A. Hasan, David M. |
author_facet | Nakagawa, Daichi Zanaty, Mario Hudson, Joseph Teferi, Nahom Ishii, Daizo Allan, Lauren Jabbour, Pascal Ortega‐Gutierrez, Santiago Samaniego, Edgar A. Hasan, David M. |
author_sort | Nakagawa, Daichi |
collection | PubMed |
description | BACKGROUND: Fragmentation of the tunica media is a hallmark of intracranial aneurysm formation, often leading to aneurysmal progression and subsequent rupture. The objective of this study is to determine the plasma level of elastin fragments in the lumen of ruptured versus unruptured human intracranial aneurysms. METHODS AND RESULTS: One hundred consecutive patients with/without ruptured saccular intracranial aneurysms undergoing endovascular coiling or stent‐assisted coiling were recruited. Blood samples were collected from the lumen of intracranial aneurysm using a microcatheter. The tip of the microcatheter was placed inside the aneurysm's sac in close proximity to the inner wall of the dome. Plasma levels of elastin fragments were measured using an ELISA‐based method. Mean plasma level of soluble human elastin fragments was significantly greater in ruptured aneurysms when compared with nonruptured aneurysms (102.0±15.5 versus 39.3±9.6 ng/mL; P<0.001). Mean plasma level of soluble human elastin fragments did not have significant correlation with age, sex, size, or aneurysm location. CONCLUSIONS: The present study revealed that a significantly higher concentration of soluble human elastin fragments in the lumen of ruptured intracranial aneurysms when compared with nonruptured ones. |
format | Online Article Text |
id | pubmed-6201439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62014392018-10-31 Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm Nakagawa, Daichi Zanaty, Mario Hudson, Joseph Teferi, Nahom Ishii, Daizo Allan, Lauren Jabbour, Pascal Ortega‐Gutierrez, Santiago Samaniego, Edgar A. Hasan, David M. J Am Heart Assoc Original Research BACKGROUND: Fragmentation of the tunica media is a hallmark of intracranial aneurysm formation, often leading to aneurysmal progression and subsequent rupture. The objective of this study is to determine the plasma level of elastin fragments in the lumen of ruptured versus unruptured human intracranial aneurysms. METHODS AND RESULTS: One hundred consecutive patients with/without ruptured saccular intracranial aneurysms undergoing endovascular coiling or stent‐assisted coiling were recruited. Blood samples were collected from the lumen of intracranial aneurysm using a microcatheter. The tip of the microcatheter was placed inside the aneurysm's sac in close proximity to the inner wall of the dome. Plasma levels of elastin fragments were measured using an ELISA‐based method. Mean plasma level of soluble human elastin fragments was significantly greater in ruptured aneurysms when compared with nonruptured aneurysms (102.0±15.5 versus 39.3±9.6 ng/mL; P<0.001). Mean plasma level of soluble human elastin fragments did not have significant correlation with age, sex, size, or aneurysm location. CONCLUSIONS: The present study revealed that a significantly higher concentration of soluble human elastin fragments in the lumen of ruptured intracranial aneurysms when compared with nonruptured ones. John Wiley and Sons Inc. 2018-08-31 /pmc/articles/PMC6201439/ /pubmed/30371156 http://dx.doi.org/10.1161/JAHA.118.010051 Text en © 2018 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Nakagawa, Daichi Zanaty, Mario Hudson, Joseph Teferi, Nahom Ishii, Daizo Allan, Lauren Jabbour, Pascal Ortega‐Gutierrez, Santiago Samaniego, Edgar A. Hasan, David M. Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm |
title | Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm |
title_full | Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm |
title_fullStr | Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm |
title_full_unstemmed | Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm |
title_short | Plasma Soluble Human Elastin Fragments as an Intra‐Aneurysmal Localized Biomarker for Ruptured Intracranial Aneurysm |
title_sort | plasma soluble human elastin fragments as an intra‐aneurysmal localized biomarker for ruptured intracranial aneurysm |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6201439/ https://www.ncbi.nlm.nih.gov/pubmed/30371156 http://dx.doi.org/10.1161/JAHA.118.010051 |
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