ID
45911
Description
Principal Investigator: Adolfo Correa, MD, MPH, PhD, Jackson Heart Study, University of Mississippi Medical Center, Jackson, MS, USA MeSH: Cardiovascular Diseases,Hypertension,Diabetes Mellitus https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000964 Since there is a greater prevalence of cardiovascular disease among African Americans, the purpose of the Jackson Heart Study (JHS) is to explore the reasons for this disparity and to uncover new approaches to reduce it. The JHS is a large, community-based, observational study whose 5306 participants were recruited from among the non-institutionalized African-American adults from urban and rural areas of the three counties (Hinds, Madison, and Rankin) that make up the Jackson, MS, metropolitan statistical area (MSA). Jackson is the capital of Mississippi, the state with the largest percentage (36.3%) of African Americans in the United States. The JHS design included participants from the Jackson ARIC study who had originally been recruited through random selection from a drivers' license registry. Approximately six months before the JHS was to begin, an amendment to the federal Driver's Privacy Protection Act was passed that changed the level of consent for public release of personal information from driver's license lists from an "opt out" to an "opt in" basis. The Mississippi Highway Patrol was no longer able to release a complete listing of all persons with driver's licenses or state identification cards, which prevented its use in the JHS. New JHS participants were chosen randomly from the Accudata America commercial listing, which provides householder name, address, zip code, phone number (if available), age group in decades, and family components. The Accudata list was deemed to provide the most complete count of households for individuals aged 55 years and older in the Jackson MSA. A structured volunteer sample was also included in which demographic cells for recruitment were designed to mirror the eligible population. Enrollment was opened to volunteers who met census-derived age, sex, and socioeconomic status (SES) eligibility criteria for the Jackson MSA. In addition, a family component was included in the JHS. The sampling frame for the family study was a participant in any one of the ARlC, random, or volunteer samples whose family size met eligibility requirements. Eligibility included having at least two full siblings and four first degree relatives (parents, siblings, children over the age of 21) who lived in the Jackson MSA and who were willing to participate in the study. No upper age limit was placed on the family sample. Known contact information was obtained during the baseline clinic examination from the index family member with a verbal pedigree format to identify name(s), age(s), address (es), and telephone number(s). Recruitment was limited to persons 35-84 years old except in the family cohort, where those 21 years old and above were eligible. Only persons who otherwise met study criteria but were deemed to be physically or mentally incompetent by trained recruiters were excluded from study eligibility.sup1/sup sup1/sup Wyatt SB, Diekelmann N, Henderson F, Andrew ME, Billingsley G, Felder SH et al. A community-driven model of research participation: the Jackson Heart Study Participant Recruitment and Retention Study. Ethn Dis 2003; 13(4):438-455 (PMID: 14632263).
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- 1/22/24 1/22/24 - Simon Heim
Copyright Holder
Adolfo Correa, MD, MPH, PhD, Jackson Heart Study, University of Mississippi Medical Center, Jackson, MS, USA
Uploaded on
January 22, 2024
DOI
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Creative Commons BY 4.0
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dbGaP phs000964 NHLBI TOPMed: The Jackson Heart Study (JHS)
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- This subject consent data table contains subject IDs, consent group information, and subject aliases.
- 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, histological type, genotyping center, sequencing center, funding source, TOPMed phase, project, and study name.
- This pedigree data table shows family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, monozygotic twin IDs, unannotated second-degree relationships, and subject's sex.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- This subject consent data table contains subject IDs, consent group information, and subject aliases.
- 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, histological type, genotyping center, sequencing center, funding source, TOPMed phase, project, and study name.
- This pedigree data table shows family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, monozygotic twin IDs, unannotated second-degree relationships, and subject's sex.
C0680251 (UMLS CUI [1,2])
C4289598 (UMLS CUI [1,2])
C1518527 (UMLS CUI [1,3])
C0007222 (UMLS CUI [1,4])
C0035648 (UMLS CUI [1,5])
C0085756 (UMLS CUI [1,6])
C0001675 (UMLS CUI [1,7])
C0237096 (UMLS CUI [1,8])
C0815251 (UMLS CUI [1,9])
C0444245 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
C2713450 (UMLS CUI [2,3])
C3846158 (UMLS CUI [2,4])
C0470187 (UMLS CUI [2,5])
C0444245 (UMLS CUI [2,6])
C0700032 (UMLS CUI [2,7])
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