A Guide for a Cardiovascular Genomics Biorepository: the CATHGEN Experience

The CATHeterization GENetics (CATHGEN) biorepository was assembled in four phases. First, project start-up began in 2000. Second, between 2001 and 2010, we collected clinical data and biological samples from 9334 individuals undergoing cardiac catheterization. Samples were matched at the individual...

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Published inJournal of cardiovascular translational research Vol. 8; no. 8; pp. 449 - 457
Main Authors Kraus, William E., Granger, Christopher B., Sketch, Michael H., Donahue, Mark P., Ginsburg, Geoffrey S., Hauser, Elizabeth R., Haynes, Carol, Newby, L. Kristin, Hurdle, Melissa, Dowdy, Z. Elaine, Shah, Svati H.
Format Journal Article
LanguageEnglish
Published New York Springer US 01.11.2015
Subjects
Online AccessGet full text
ISSN1937-5387
1937-5395
DOI10.1007/s12265-015-9648-y

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Abstract The CATHeterization GENetics (CATHGEN) biorepository was assembled in four phases. First, project start-up began in 2000. Second, between 2001 and 2010, we collected clinical data and biological samples from 9334 individuals undergoing cardiac catheterization. Samples were matched at the individual level to clinical data collected at the time of catheterization and stored in the Duke Databank for Cardiovascular Diseases (DDCD). Clinical data included the following: subject demographics (birth date, race, gender, etc.); cardiometabolic history including symptoms; coronary anatomy and cardiac function at catheterization; and fasting chemistry data. Third, as part of the DDCD regular follow-up protocol, yearly evaluations included interim information: vital status (verified via National Death Index search and supplemented by Social Security Death Index search), myocardial infarction (MI), stroke, rehospitalization, coronary revascularization procedures, medication use, and lifestyle habits including smoking. Fourth, samples were used to generate molecular data. CATHGEN offers the opportunity to discover biomarkers and explore mechanisms of cardiovascular disease.
AbstractList The CATHeterization GENetics (CATHGEN) biorepository was assembled in four phases. First, project start-up began in 2000. Second, between 2001 and 2010, we collected clinical data and biological samples from 9334 individuals undergoing cardiac catheterization. Samples were matched at the individual level to clinical data collected at the time of catheterization and stored in the Duke Databank for Cardiovascular Diseases (DDCD). Clinical data included the following: subject demographics (birth date, race, gender, etc.); cardiometabolic history including symptoms; coronary anatomy and cardiac function at catheterization; and fasting chemistry data. Third, as part of the DDCD regular follow-up protocol, yearly evaluations included interim information: vital status (verified via National Death Index search and supplemented by Social Security Death Index search), myocardial infarction (MI), stroke, rehospitalization, coronary revascularization procedures, medication use, and lifestyle habits including smoking. Fourth, samples were used to generate molecular data. CATHGEN offers the opportunity to discover biomarkers and explore mechanisms of cardiovascular disease.
The CATHGEN Biorepository was assembled in four phases. First, project startup began in 2000. Second, between 2001 and 2010, we collected clinical data and biological samples from 9334 individuals undergoing cardiac catheterization. Samples were matched at the individual level to clinical data collected at the time of catheterization and stored in the Duke Databank for Cardiovascular Diseases (DDCD). Clinical data included: subject demographics (birthdate, race, gender, etc.); cardiometabolic history including symptoms; coronary anatomy and cardiac function at catheterization; and fasting chemistry data. Third, as part of the DDCD regular follow-up protocol, yearly evaluations included interim information: vital status (verified via National Death Index search and supplemented by Social Security Death Index search), myocardial infarction (MI), stroke, rehospitalization, coronary revascularization procedures, medication use, and lifestyle habits including smoking. Fourth, samples were used to generate molecular data. CATHGEN offers the opportunity to discover biomarkers and explore mechanisms of cardiovascular disease.
Author Granger, Christopher B.
Sketch, Michael H.
Shah, Svati H.
Kraus, William E.
Haynes, Carol
Donahue, Mark P.
Hurdle, Melissa
Dowdy, Z. Elaine
Newby, L. Kristin
Ginsburg, Geoffrey S.
Hauser, Elizabeth R.
AuthorAffiliation 4 Duke Center for Applied Genomics and Precision Medicine, Durham, NC 27710
2 Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC 27710
1 Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC 27710
3 Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC 27710
AuthorAffiliation_xml – name: 3 Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC 27710
– name: 4 Duke Center for Applied Genomics and Precision Medicine, Durham, NC 27710
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– name: 1 Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC 27710
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  givenname: William E.
  orcidid: 0000-0003-1930-9684
  surname: Kraus
  fullname: Kraus, William E.
  email: william.kraus@duke.edu
  organization: Division of Cardiology, Department of Medicine, School of Medicine, Duke University, Duke Molecular Physiology Institute, School of Medicine, Duke University
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  givenname: Christopher B.
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  organization: Division of Cardiology, Department of Medicine, School of Medicine, Duke University
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  givenname: Geoffrey S.
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  fullname: Ginsburg, Geoffrey S.
  organization: Duke Center for Applied Genomics and Precision Medicine, Duke University
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  givenname: Elizabeth R.
  surname: Hauser
  fullname: Hauser, Elizabeth R.
  organization: Division of Cardiology, Department of Medicine, School of Medicine, Duke University, Duke Molecular Physiology Institute, School of Medicine, Duke University
– sequence: 7
  givenname: Carol
  surname: Haynes
  fullname: Haynes, Carol
  organization: Duke Molecular Physiology Institute, School of Medicine, Duke University
– sequence: 8
  givenname: L. Kristin
  surname: Newby
  fullname: Newby, L. Kristin
  organization: Division of Cardiology, Department of Medicine, School of Medicine, Duke University, Duke Clinical Research Institute, School of Medicine, Duke University
– sequence: 9
  givenname: Melissa
  surname: Hurdle
  fullname: Hurdle, Melissa
  organization: Duke Molecular Physiology Institute, School of Medicine, Duke University
– sequence: 10
  givenname: Z. Elaine
  surname: Dowdy
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  givenname: Svati H.
  surname: Shah
  fullname: Shah, Svati H.
  organization: Division of Cardiology, Department of Medicine, School of Medicine, Duke University, Duke Molecular Physiology Institute, School of Medicine, Duke University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26271459$$D View this record in MEDLINE/PubMed
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Issue 8
Keywords Metabolomics
Cardiometabolic disease
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Biorepository
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Cardiovascular disease
Genetics
Air pollution
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Bhattacharya, Dunham, Cornish, Christian, Ginsburg, Tenenbaum (CR1) 2012; 4
Lappe, Horne, Shah, May, Muhlestein, Lappe (CR20) 2011; 412
Minear, Crosslin, Sutton, Connelly, Nelson, Gadson-Watson (CR21) 2011; 129
Rosenberg, Elashoff, Beineke, Daniels, Wingrove, Tingley (CR24) 2010; 153
Shah, Craig, Sebek, Haynes, Stevens, Muehlbauer (CR27) 2012; 143
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Bhattacharya, Granger, Craig, Haynes, Bain, Stevens (CR5) 2014; 232
Rosenberg, Elashoff, Lieu, Brown, Kraus, Schwartz (CR25) 2012; 5
Connelly, Cherepanova, Doss, Karaoli, Lillard, Markunas (CR7) 2013; 22
Ward-Caviness, Haynes, Blach, Dowdy, Gregory, Shah (CR40) 2013; 132
Jeyarajah, Cromwell, Otvos (CR3) 2006; 26
Dungan, Hauser, Qin, Kraus (CR14) 2013; 4
Elashoff, Wingrove, Beineke, Daniels, Tingley, Rosenberg (CR15) 2011; 4
Shah, Granger, Hauser, Kraus, Sun, Pieper (CR30) 2010; 160
Halim, Neely, Pieper, Shah, Kraus, Hauser (CR2) 2015; 8
CR41
Beineke, Fitch, Tao, Elashoff, Rosenberg, Kraus (CR4) 2012; 5
Shah, Freedman, Zhang, Crosslin, Stone, Haynes (CR29) 2009; 5
Shah, Hauser, Crosslin, Wang, Haynes, Connelly (CR31) 2008; 201
Sutton, Crosslin, Shah, Nelson, Bassil, Hale (CR35) 2008; 17
Davies, Wells, Stewart, Erdmann, Shah, Ferguson (CR12) 2012; 5
Kral, Mathias, Suktitipat, Ruczinski, Vaidya, Yanek (CR18) 2011; 56
Crosslin, Shah, Nelson, Haynes, Connelly, Gadson (CR10) 2009; 125
MR Elashoff (9648_CR15) 2011; 4
AJ Sehnert (9648_CR26) 2008; 52
SH Shah (9648_CR30) 2010; 160
BG Kral (9648_CR18) 2011; 56
AA Shah (9648_CR27) 2012; 143
SH Shah (9648_CR28) 2010; 3
GM Peloso (9648_CR23) 2014; 94
MD Kertai (9648_CR17) 2014; 7
BD Horne (9648_CR16) 2009; 73
S Rosenberg (9648_CR24) 2010; 153
L Wang (9648_CR38) 2007; 80
SE Daniels (9648_CR11) 2014; 7
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Snippet The CATHeterization GENetics (CATHGEN) biorepository was assembled in four phases. First, project start-up began in 2000. Second, between 2001 and 2010, we...
The CATHGEN Biorepository was assembled in four phases. First, project startup began in 2000. Second, between 2001 and 2010, we collected clinical data and...
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SubjectTerms Biological Specimen Banks - organization & administration
Biomedical Engineering and Bioengineering
Biomedicine
Cardiology
Cardiovascular Diseases - diagnosis
Cardiovascular Diseases - genetics
Cardiovascular Diseases - therapy
Databases, Genetic
Gene Expression Profiling
Gene-Environment Interaction
Genetic Association Studies
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing - methods
Genomics - methods
Genomics - organization & administration
Human Genetics
Humans
Intellectual Property
Medicine
Medicine & Public Health
Models, Organizational
Phenotype
Predictive Value of Tests
Prognosis
Risk Factors
Specimen Handling
Time Factors
Title A Guide for a Cardiovascular Genomics Biorepository: the CATHGEN Experience
URI https://link.springer.com/article/10.1007/s12265-015-9648-y
https://www.ncbi.nlm.nih.gov/pubmed/26271459
https://www.proquest.com/docview/1735326966
https://pubmed.ncbi.nlm.nih.gov/PMC4651812
Volume 8
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