ID
45839
Beskrivning
Principal Investigator: Dan Roden, MD, Vanderbilt University, Nashville, TN,USA MeSH: Atrial Fibrillation https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001032 The Vanderbilt Atrial Fibrillation (AF) Registry was founded in 2001. Patients with AF and family members are prospectively enrolled. At enrollment a detailed past medical history is obtained along with an AF symptom severity assessment. Blood samples are obtained for DNA extraction. Patients are followed longitudinally along with serial collection of AF symptom severity assessments.
Länk
Nyckelord
Versioner (1)
- 2023-08-15 2023-08-15 - Simon Heim
Rättsinnehavare
Dan Roden, MD, Vanderbilt University, Nashville, TN,USA
Uppladdad den
15 augusti 2023
DOI
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Licens
Creative Commons BY 4.0
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dbGaP phs001032 NHLBI TOPMed: The Vanderbilt Atrial Fibrillation Registry (VU_AF)
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent data table contains subject IDs, consent group information, subject aliases, and affection status for atrial fibrillation (AF).
- This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
- This sample attributes table includes body site where sample was collected, analyte type, tumor status, sequencing center, funding source, TOPMed phase, project, and study name.
- This subject phenotype data table includes atrial fibrillation (AF) status, age at enrollment and AF diagnosis, sex, race, ethnicity, height, and weight. At enrollment, hypertension, diabetes, heart failure, myocardial infarction, and valvular heart disease (n=2 variables) statuses were determined. Additionally, LA size and LVEF measurements were determined.
- The pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and subject's sex.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent data table contains subject IDs, consent group information, subject aliases, and affection status for atrial fibrillation (AF).
- This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
- This sample attributes table includes body site where sample was collected, analyte type, tumor status, sequencing center, funding source, TOPMed phase, project, and study name.
- This subject phenotype data table includes atrial fibrillation (AF) status, age at enrollment and AF diagnosis, sex, race, ethnicity, height, and weight. At enrollment, hypertension, diabetes, heart failure, myocardial infarction, and valvular heart disease (n=2 variables) statuses were determined. Additionally, LA size and LVEF measurements were determined.
- The pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and subject's sex.
C0680251 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,2])
C0086282 (UMLS CUI [1,3])
C5419021 (UMLS CUI [1,4])
C0242802 (UMLS CUI [2,1])
C0004238 (UMLS CUI [2,2])
C0814120 (UMLS CUI [2,3])
C1561491 (UMLS CUI [2,4])