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Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm

BACKGROUND: Intracranial aneurysm (IA) is significantly more prevalent in patients with coarctation of the aorta or bicuspid aortic valve than in the general population, suggesting a common pathophysiology connecting IA and aortopathy. Here, we analyzed echocardiographic aortic root dimension (ARD)...

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Autores principales: Shin, Yong-Won, Jung, Keun-Hwa, Kim, Jeong-Min, Cho, Young Dae, Lee, Soon-Tae, Chu, Kon, Kim, Manho, Lee, Sang Kun, Han, Moon Hee, Roh, Jae-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070985/
https://www.ncbi.nlm.nih.gov/pubmed/24964197
http://dx.doi.org/10.1371/journal.pone.0100569
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author Shin, Yong-Won
Jung, Keun-Hwa
Kim, Jeong-Min
Cho, Young Dae
Lee, Soon-Tae
Chu, Kon
Kim, Manho
Lee, Sang Kun
Han, Moon Hee
Roh, Jae-Kyu
author_facet Shin, Yong-Won
Jung, Keun-Hwa
Kim, Jeong-Min
Cho, Young Dae
Lee, Soon-Tae
Chu, Kon
Kim, Manho
Lee, Sang Kun
Han, Moon Hee
Roh, Jae-Kyu
author_sort Shin, Yong-Won
collection PubMed
description BACKGROUND: Intracranial aneurysm (IA) is significantly more prevalent in patients with coarctation of the aorta or bicuspid aortic valve than in the general population, suggesting a common pathophysiology connecting IA and aortopathy. Here, we analyzed echocardiographic aortic root dimension (ARD) in patients with IA to confirm this possibility. METHODS: From January 2008 to December 2010, 260 consecutive patients with IA who were admitted to our institution for coil embolization or for acute stroke management and who also underwent echocardiography were enrolled. We hypothesized that patients with large, ruptured, or multiple IAs are more likely to harbor co-prevalent aortopathy as measured by ARD compared to patients with small, isolated, unruptured IAs. Eccentric group was defined as patients aged <55 years with at least one ruptured aneurysm, an aneurysm ≥7 mm in size, or multiple aneurysms; the remainder was classified into a non-eccentric group. Clinical, angiographic, and echocardiographic findings of the two groups were compared. RESULTS: ARD was significantly larger in the eccentric group than in the non-eccentric group (P = 0.049), and the difference was confirmed by multivariable analysis (P = 0.02). Subgroup analysis of patients aged <55 years showed similar result for ARD (P = 0.03), whereas hypertension was more associated with the non-eccentric group (P = 0.01). In addition, height was inversely related to aneurysm size after adjustment for age, sex, weight, ARD, smoking status, and number of aneurysms (P = 0.004). CONCLUSIONS: A certain group of IA patients share a common intrinsic wall defect with aortopathy. Shared neural crest cell origin may give rise to this phenomenon.
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spelling pubmed-40709852014-06-27 Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm Shin, Yong-Won Jung, Keun-Hwa Kim, Jeong-Min Cho, Young Dae Lee, Soon-Tae Chu, Kon Kim, Manho Lee, Sang Kun Han, Moon Hee Roh, Jae-Kyu PLoS One Research Article BACKGROUND: Intracranial aneurysm (IA) is significantly more prevalent in patients with coarctation of the aorta or bicuspid aortic valve than in the general population, suggesting a common pathophysiology connecting IA and aortopathy. Here, we analyzed echocardiographic aortic root dimension (ARD) in patients with IA to confirm this possibility. METHODS: From January 2008 to December 2010, 260 consecutive patients with IA who were admitted to our institution for coil embolization or for acute stroke management and who also underwent echocardiography were enrolled. We hypothesized that patients with large, ruptured, or multiple IAs are more likely to harbor co-prevalent aortopathy as measured by ARD compared to patients with small, isolated, unruptured IAs. Eccentric group was defined as patients aged <55 years with at least one ruptured aneurysm, an aneurysm ≥7 mm in size, or multiple aneurysms; the remainder was classified into a non-eccentric group. Clinical, angiographic, and echocardiographic findings of the two groups were compared. RESULTS: ARD was significantly larger in the eccentric group than in the non-eccentric group (P = 0.049), and the difference was confirmed by multivariable analysis (P = 0.02). Subgroup analysis of patients aged <55 years showed similar result for ARD (P = 0.03), whereas hypertension was more associated with the non-eccentric group (P = 0.01). In addition, height was inversely related to aneurysm size after adjustment for age, sex, weight, ARD, smoking status, and number of aneurysms (P = 0.004). CONCLUSIONS: A certain group of IA patients share a common intrinsic wall defect with aortopathy. Shared neural crest cell origin may give rise to this phenomenon. Public Library of Science 2014-06-25 /pmc/articles/PMC4070985/ /pubmed/24964197 http://dx.doi.org/10.1371/journal.pone.0100569 Text en © 2014 Shin 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
Shin, Yong-Won
Jung, Keun-Hwa
Kim, Jeong-Min
Cho, Young Dae
Lee, Soon-Tae
Chu, Kon
Kim, Manho
Lee, Sang Kun
Han, Moon Hee
Roh, Jae-Kyu
Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm
title Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm
title_full Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm
title_fullStr Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm
title_full_unstemmed Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm
title_short Echocardiographic Evidence of Innate Aortopathy in the Human Intracranial Aneurysm
title_sort echocardiographic evidence of innate aortopathy in the human intracranial aneurysm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070985/
https://www.ncbi.nlm.nih.gov/pubmed/24964197
http://dx.doi.org/10.1371/journal.pone.0100569
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