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Cohort profile: the Emory Cardiovascular Biobank (EmCAB)

PURPOSE: The Emory Cardiovascular Biobank (EmCAB) is an ongoing prospective registry of patients undergoing cardiac catheterisation, which was established to identify novel factors associated with the pathobiological process and treatment of cardiovascular disease. PARTICIPANTS: Individuals aged 18...

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Autores principales: Ko, Yi-An, Hayek, Salim, Sandesara, Pratik, Samman Tahhan, Ayman, Quyyumi, Arshed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778297/
https://www.ncbi.nlm.nih.gov/pubmed/29288185
http://dx.doi.org/10.1136/bmjopen-2017-018753
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author Ko, Yi-An
Hayek, Salim
Sandesara, Pratik
Samman Tahhan, Ayman
Quyyumi, Arshed
author_facet Ko, Yi-An
Hayek, Salim
Sandesara, Pratik
Samman Tahhan, Ayman
Quyyumi, Arshed
author_sort Ko, Yi-An
collection PubMed
description PURPOSE: The Emory Cardiovascular Biobank (EmCAB) is an ongoing prospective registry of patients undergoing cardiac catheterisation, which was established to identify novel factors associated with the pathobiological process and treatment of cardiovascular disease. PARTICIPANTS: Individuals aged 18 years and older undergoing cardiac catheterisation at three Emory Healthcare sites in Atlanta are asked to participate in this prospective registry. Around 95% agree to participate. Around 7000 unique patients have been enrolled. The current data set contains detailed phenotyping, patient outcomes, genomics, protein biomarkers, regenerative markers, transcriptomic analysis, metabolomics profiling and longitudinal follow-up for adverse cardiovascular outcomes. FINDINGS TO DATE: Thus far, the EmCAB has approximately 3000 major cardiovascular events. About 48% of the EmCAB participants have more than 5 years of follow-up. It is a great resource for discovery of novel predictive factors for cardiovascular disease outcomes, including genomics, transcriptomics, protein biomarkers, oxidative stress markers and circulating progenitor cells. Several circulating inflammatory markers have shown to improve risk prediction metrics beyond standard risk factors. FUTURE PLANS: Future integrative –omics analyses will provide the cardiovascular research community opportunities for subsequent mechanistic confirmation studies, which will promote the development of effective personalised therapy that leads to clinical care tailored to the individual patient.
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spelling pubmed-57782972018-01-31 Cohort profile: the Emory Cardiovascular Biobank (EmCAB) Ko, Yi-An Hayek, Salim Sandesara, Pratik Samman Tahhan, Ayman Quyyumi, Arshed BMJ Open Cardiovascular Medicine PURPOSE: The Emory Cardiovascular Biobank (EmCAB) is an ongoing prospective registry of patients undergoing cardiac catheterisation, which was established to identify novel factors associated with the pathobiological process and treatment of cardiovascular disease. PARTICIPANTS: Individuals aged 18 years and older undergoing cardiac catheterisation at three Emory Healthcare sites in Atlanta are asked to participate in this prospective registry. Around 95% agree to participate. Around 7000 unique patients have been enrolled. The current data set contains detailed phenotyping, patient outcomes, genomics, protein biomarkers, regenerative markers, transcriptomic analysis, metabolomics profiling and longitudinal follow-up for adverse cardiovascular outcomes. FINDINGS TO DATE: Thus far, the EmCAB has approximately 3000 major cardiovascular events. About 48% of the EmCAB participants have more than 5 years of follow-up. It is a great resource for discovery of novel predictive factors for cardiovascular disease outcomes, including genomics, transcriptomics, protein biomarkers, oxidative stress markers and circulating progenitor cells. Several circulating inflammatory markers have shown to improve risk prediction metrics beyond standard risk factors. FUTURE PLANS: Future integrative –omics analyses will provide the cardiovascular research community opportunities for subsequent mechanistic confirmation studies, which will promote the development of effective personalised therapy that leads to clinical care tailored to the individual patient. BMJ Publishing Group 2017-12-29 /pmc/articles/PMC5778297/ /pubmed/29288185 http://dx.doi.org/10.1136/bmjopen-2017-018753 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 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 Cardiovascular Medicine
Ko, Yi-An
Hayek, Salim
Sandesara, Pratik
Samman Tahhan, Ayman
Quyyumi, Arshed
Cohort profile: the Emory Cardiovascular Biobank (EmCAB)
title Cohort profile: the Emory Cardiovascular Biobank (EmCAB)
title_full Cohort profile: the Emory Cardiovascular Biobank (EmCAB)
title_fullStr Cohort profile: the Emory Cardiovascular Biobank (EmCAB)
title_full_unstemmed Cohort profile: the Emory Cardiovascular Biobank (EmCAB)
title_short Cohort profile: the Emory Cardiovascular Biobank (EmCAB)
title_sort cohort profile: the emory cardiovascular biobank (emcab)
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778297/
https://www.ncbi.nlm.nih.gov/pubmed/29288185
http://dx.doi.org/10.1136/bmjopen-2017-018753
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