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Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol

INTRODUCTION: Cerebral venous thrombosis (CVT) is a rare cerebrovascular condition accounting for <1% of all stroke cases and mainly affects young adults. Its genetic aetiology is not clearly elucidated. METHODS AND ANALYSIS: To better understand the genetic basis of CVT, we have established an i...

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Autores principales: Cotlarciuc, Ioana, Marjot, Thomas, Khan, Muhammad S, Hiltunen, Sini, Haapaniemi, Elena, Metso, Tiina M, Putaala, Jukka, Zuurbier, Susanna M, Brouwer, Matthijs C, Passamonti, Serena M, Bucciarelli, Paolo, Pappalardo, Emanuela, Patel, Tasmin, Costa, Paolo, Colombi, Marina, Canhão, Patrícia, Tkach, Aleksander, Santacroce, Rosa, Margaglione, Maurizio, Favuzzi, Giovanni, Grandone, Elvira, Colaizzo, Donatella, Spengos, Kostas, Arauz, Antonio, Hodge, Amanda, Ditta, Reina, Debette, Stephanie, Zedde, Marialuisa, Pare, Guillaume, Ferro, José M, Thijs, Vincent, Pezzini, Alessandro, Majersik, Jennifer J, Martinelli, Ida, Coutinho, Jonathan M, Tatlisumak, Turgut, Sharma, Pankaj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128947/
https://www.ncbi.nlm.nih.gov/pubmed/27881526
http://dx.doi.org/10.1136/bmjopen-2016-012351
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author Cotlarciuc, Ioana
Marjot, Thomas
Khan, Muhammad S
Hiltunen, Sini
Haapaniemi, Elena
Metso, Tiina M
Putaala, Jukka
Zuurbier, Susanna M
Brouwer, Matthijs C
Passamonti, Serena M
Bucciarelli, Paolo
Pappalardo, Emanuela
Patel, Tasmin
Costa, Paolo
Colombi, Marina
Canhão, Patrícia
Tkach, Aleksander
Santacroce, Rosa
Margaglione, Maurizio
Favuzzi, Giovanni
Grandone, Elvira
Colaizzo, Donatella
Spengos, Kostas
Arauz, Antonio
Hodge, Amanda
Ditta, Reina
Debette, Stephanie
Zedde, Marialuisa
Pare, Guillaume
Ferro, José M
Thijs, Vincent
Pezzini, Alessandro
Majersik, Jennifer J
Martinelli, Ida
Coutinho, Jonathan M
Tatlisumak, Turgut
Sharma, Pankaj
author_facet Cotlarciuc, Ioana
Marjot, Thomas
Khan, Muhammad S
Hiltunen, Sini
Haapaniemi, Elena
Metso, Tiina M
Putaala, Jukka
Zuurbier, Susanna M
Brouwer, Matthijs C
Passamonti, Serena M
Bucciarelli, Paolo
Pappalardo, Emanuela
Patel, Tasmin
Costa, Paolo
Colombi, Marina
Canhão, Patrícia
Tkach, Aleksander
Santacroce, Rosa
Margaglione, Maurizio
Favuzzi, Giovanni
Grandone, Elvira
Colaizzo, Donatella
Spengos, Kostas
Arauz, Antonio
Hodge, Amanda
Ditta, Reina
Debette, Stephanie
Zedde, Marialuisa
Pare, Guillaume
Ferro, José M
Thijs, Vincent
Pezzini, Alessandro
Majersik, Jennifer J
Martinelli, Ida
Coutinho, Jonathan M
Tatlisumak, Turgut
Sharma, Pankaj
author_sort Cotlarciuc, Ioana
collection PubMed
description INTRODUCTION: Cerebral venous thrombosis (CVT) is a rare cerebrovascular condition accounting for <1% of all stroke cases and mainly affects young adults. Its genetic aetiology is not clearly elucidated. METHODS AND ANALYSIS: To better understand the genetic basis of CVT, we have established an international biobank of CVT cases, Biorepository to Establish the Aetiology of Sinovenous Thrombosis (BEAST) which aims to recruit highly phenotyped cases initially of European descent and later from other populations. To date we have recruited 745 CVT cases from 12 research centres. As an initial step, the consortium plans to undertake a genome-wide association analysis of CVT using the Illumina Infinium HumanCoreExome BeadChip to assess the association and impact of common and low-frequency genetic variants on CVT risk by using a case–control study design. Replication will be performed to confirm putative findings. Furthermore, we aim to identify interactions of genetic variants with several environmental and comorbidity factors which will likely contribute to improve the understanding of the biological mechanisms underlying this complex disease. ETHICS AND DISSEMINATION: BEAST meets all ethical standards set by local institutional review boards for each of the participating sites. The research outcomes will be published in international peer-reviewed open-access journals with high impact and visibility. The results will be presented at national and international meetings to highlight the contributions into improving the understanding of the mechanisms underlying this uncommon but important disease. This international DNA repository will become an important resource for investigators in the field of haematological and vascular disorders.
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spelling pubmed-51289472016-12-02 Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol Cotlarciuc, Ioana Marjot, Thomas Khan, Muhammad S Hiltunen, Sini Haapaniemi, Elena Metso, Tiina M Putaala, Jukka Zuurbier, Susanna M Brouwer, Matthijs C Passamonti, Serena M Bucciarelli, Paolo Pappalardo, Emanuela Patel, Tasmin Costa, Paolo Colombi, Marina Canhão, Patrícia Tkach, Aleksander Santacroce, Rosa Margaglione, Maurizio Favuzzi, Giovanni Grandone, Elvira Colaizzo, Donatella Spengos, Kostas Arauz, Antonio Hodge, Amanda Ditta, Reina Debette, Stephanie Zedde, Marialuisa Pare, Guillaume Ferro, José M Thijs, Vincent Pezzini, Alessandro Majersik, Jennifer J Martinelli, Ida Coutinho, Jonathan M Tatlisumak, Turgut Sharma, Pankaj BMJ Open Neurology INTRODUCTION: Cerebral venous thrombosis (CVT) is a rare cerebrovascular condition accounting for <1% of all stroke cases and mainly affects young adults. Its genetic aetiology is not clearly elucidated. METHODS AND ANALYSIS: To better understand the genetic basis of CVT, we have established an international biobank of CVT cases, Biorepository to Establish the Aetiology of Sinovenous Thrombosis (BEAST) which aims to recruit highly phenotyped cases initially of European descent and later from other populations. To date we have recruited 745 CVT cases from 12 research centres. As an initial step, the consortium plans to undertake a genome-wide association analysis of CVT using the Illumina Infinium HumanCoreExome BeadChip to assess the association and impact of common and low-frequency genetic variants on CVT risk by using a case–control study design. Replication will be performed to confirm putative findings. Furthermore, we aim to identify interactions of genetic variants with several environmental and comorbidity factors which will likely contribute to improve the understanding of the biological mechanisms underlying this complex disease. ETHICS AND DISSEMINATION: BEAST meets all ethical standards set by local institutional review boards for each of the participating sites. The research outcomes will be published in international peer-reviewed open-access journals with high impact and visibility. The results will be presented at national and international meetings to highlight the contributions into improving the understanding of the mechanisms underlying this uncommon but important disease. This international DNA repository will become an important resource for investigators in the field of haematological and vascular disorders. BMJ Publishing Group 2016-11-22 /pmc/articles/PMC5128947/ /pubmed/27881526 http://dx.doi.org/10.1136/bmjopen-2016-012351 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Neurology
Cotlarciuc, Ioana
Marjot, Thomas
Khan, Muhammad S
Hiltunen, Sini
Haapaniemi, Elena
Metso, Tiina M
Putaala, Jukka
Zuurbier, Susanna M
Brouwer, Matthijs C
Passamonti, Serena M
Bucciarelli, Paolo
Pappalardo, Emanuela
Patel, Tasmin
Costa, Paolo
Colombi, Marina
Canhão, Patrícia
Tkach, Aleksander
Santacroce, Rosa
Margaglione, Maurizio
Favuzzi, Giovanni
Grandone, Elvira
Colaizzo, Donatella
Spengos, Kostas
Arauz, Antonio
Hodge, Amanda
Ditta, Reina
Debette, Stephanie
Zedde, Marialuisa
Pare, Guillaume
Ferro, José M
Thijs, Vincent
Pezzini, Alessandro
Majersik, Jennifer J
Martinelli, Ida
Coutinho, Jonathan M
Tatlisumak, Turgut
Sharma, Pankaj
Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol
title Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol
title_full Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol
title_fullStr Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol
title_full_unstemmed Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol
title_short Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol
title_sort towards the genetic basis of cerebral venous thrombosis—the beast consortium: a study protocol
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128947/
https://www.ncbi.nlm.nih.gov/pubmed/27881526
http://dx.doi.org/10.1136/bmjopen-2016-012351
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