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Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach
BACKGROUND: Small or hypoplastic vertebral artery (VA) is one of the risk factor for posterior circulation stroke. We assess whether various types of VA anomaly contribute to its diameter. METHODS: We screened 238 patients who underwent neck CT and MR angiography within 1 month. A V1 anomaly was def...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576129/ https://www.ncbi.nlm.nih.gov/pubmed/28851303 http://dx.doi.org/10.1186/s12883-017-0951-x |
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author | Kim, Chulho Sohn, Jong-Hee Choi, Hui-Chul |
author_facet | Kim, Chulho Sohn, Jong-Hee Choi, Hui-Chul |
author_sort | Kim, Chulho |
collection | PubMed |
description | BACKGROUND: Small or hypoplastic vertebral artery (VA) is one of the risk factor for posterior circulation stroke. We assess whether various types of VA anomaly contribute to its diameter. METHODS: We screened 238 patients who underwent neck CT and MR angiography within 1 month. A V1 anomaly was defined as the abnormal origin of the VA on a three-dimensional MR angiography and a V2 anomaly was defined as the VA not passing through the 6th cervical transverse foramen (TF) on an axial CT image. A linear mixed model was used to evaluate the determinants of VA size. RESULTS: Among participants, 24 (10.1%) subjects exhibited an anomalous VA and, of the 476 VAs examined, 11 (2.3%) had an aortic origin and 27 (5.7%) had an abnormal entrance into the C6 TF. Presence of the V1 anomaly was positively associated with the V2 anomaly (P for chi-square < 0.001) and a linear mixed model revealed that being male (0.2 mm larger, P = 0.015), having a right VA anomaly (0.3 mm smaller, P < 0.001), having a V1 anomaly (0.9 mm smaller, P < 0.001), and having a V2 anomaly (0.7 mm smaller, P < 0.001) were significant predictor of VA diameter. CONCLUSION: The diameters of VAs with an anomalous aortic origin or an abnormal entrance of the TF were significantly smaller than those of normal VAs. These findings suggest that anomalies of the VA detected in 3-dimensional CTA or MRA may be clues for vertebral artery hypoplasia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12883-017-0951-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5576129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55761292017-08-30 Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach Kim, Chulho Sohn, Jong-Hee Choi, Hui-Chul BMC Neurol Research Article BACKGROUND: Small or hypoplastic vertebral artery (VA) is one of the risk factor for posterior circulation stroke. We assess whether various types of VA anomaly contribute to its diameter. METHODS: We screened 238 patients who underwent neck CT and MR angiography within 1 month. A V1 anomaly was defined as the abnormal origin of the VA on a three-dimensional MR angiography and a V2 anomaly was defined as the VA not passing through the 6th cervical transverse foramen (TF) on an axial CT image. A linear mixed model was used to evaluate the determinants of VA size. RESULTS: Among participants, 24 (10.1%) subjects exhibited an anomalous VA and, of the 476 VAs examined, 11 (2.3%) had an aortic origin and 27 (5.7%) had an abnormal entrance into the C6 TF. Presence of the V1 anomaly was positively associated with the V2 anomaly (P for chi-square < 0.001) and a linear mixed model revealed that being male (0.2 mm larger, P = 0.015), having a right VA anomaly (0.3 mm smaller, P < 0.001), having a V1 anomaly (0.9 mm smaller, P < 0.001), and having a V2 anomaly (0.7 mm smaller, P < 0.001) were significant predictor of VA diameter. CONCLUSION: The diameters of VAs with an anomalous aortic origin or an abnormal entrance of the TF were significantly smaller than those of normal VAs. These findings suggest that anomalies of the VA detected in 3-dimensional CTA or MRA may be clues for vertebral artery hypoplasia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12883-017-0951-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-29 /pmc/articles/PMC5576129/ /pubmed/28851303 http://dx.doi.org/10.1186/s12883-017-0951-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kim, Chulho Sohn, Jong-Hee Choi, Hui-Chul Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach |
title | Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach |
title_full | Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach |
title_fullStr | Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach |
title_full_unstemmed | Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach |
title_short | Are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach |
title_sort | are the anomalous vertebral arteries more hypoplastic?: retrospective linear mixed model approach |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576129/ https://www.ncbi.nlm.nih.gov/pubmed/28851303 http://dx.doi.org/10.1186/s12883-017-0951-x |
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