ID

45631

Description

Principal Investigator: Sharon L.R. Kardia, PhD, University of Michigan, Ann Arbor, MI, USA MeSH: Hypertension,Aging,Arterial Pressure,Arteriosclerosis,Atherosclerosis,Biomarkers,Blood Pressure,Cardiovascular Diseases,Cholesterol,Cholesterol, HDL,Cholesterol, LDL,Coronary Artery Disease,Diabetes Mellitus,Echocardiography,Endophenotypes,Hyperglycemia,Hyperinsulinism,Hypertrophy, Left Ventricular,Inflammation,Kidney Failure, Chronic,Leukoaraiosis,Lipids,Obesity,Obesity, Abdominal,Peripheral Arterial Disease,Renal Insufficiency, Chronic,Triglycerides,Vascular Calcification https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001345 The Genetic Epidemiology Network of Arteriopathy (GENOA) is one of four networks in the NHLBI Family-Blood Pressure Program (FBPP). GENOA's long-term objective is to elucidate the genetics of target organ complications of hypertension, including both atherosclerotic and arteriolosclerotic complications involving the heart, brain, kidneys, and peripheral arteries. The longitudinal GENOA Study recruited European-American and African-American sibships with at least 2 individuals with clinically diagnosed essential hypertension before age 60 years. All other members of the sibship were invited to participate regardless of their hypertension status. Participants were diagnosed with hypertension if they had either 1) a previous clinical diagnosis of hypertension by a physician with current anti-hypertensive treatment, or 2) an average systolic blood pressure = 140 mm Hg or diastolic blood pressure = 90 mm Hg based on the second and third readings at the time of their clinic visit. Only participants of the African-American Cohort were sequenced through TOPMed. The Family Blood Pressure Program (FBPP), GENOA's parent program, is an unprecedented collaboration to identify genes influencing blood pressure (BP) levels, hypertension, and its target-organ damage. This program has conducted over 21,000 physical examinations, assembled a shared database of several hundred BP and hypertension-related phenotypic measurements, completed genome-wide linkage analyses for BP, hypertension, and hypertension associated risk factors and complications, and published over 130 manuscripts on program findings. The FBPP emerged from what was initially funded as four independent networks of investigators (HyperGEN, GenNet, SAPPHIRe and GENOA) competing to identify genetic determinants of hypertension in multiple ethnic groups. Realizing the greater likelihood of success through collaboration, the investigators created a single confederation with program-wide and network-specific goals. Comprehensive phenotypic data for GENOA study participants are available through dbGaP phs001238.

Link

dbGaP study = phs001345

Keywords

  1. 3/5/23 3/5/23 - Simon Heim
Copyright Holder

Sharon L.R. Kardia, PhD, University of Michigan, Ann Arbor, MI, USA

Uploaded on

March 5, 2023

DOI

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License

Creative Commons BY 4.0

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dbGaP phs001345 NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA)

The subject consent data table contains subject IDs, consent group information, and subject aliases.

pht008602
Description

pht008602

Alias
UMLS CUI [1,1]
C3846158
De-identified Subject Identifier
Description

SUBJECT_ID

Data type

string

Alias
UMLS CUI [1,1]
C4684638
UMLS CUI [1,2]
C2348585
Consent Group
Description

CONSENT

Data type

text

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0441833
Repository name for dbGaP study also containing this individual
Description

SUBJECT_SOURCE

Data type

string

Alias
UMLS CUI [1,1]
C5669549
UMLS CUI [1,2]
C0947630
UMLS CUI [1,3]
C3846158
Subject ID used in the SUBJECT_SOURCE repository
Description

SOURCE_SUBJECT_ID

Data type

string

Alias
UMLS CUI [1,1]
C2348585
UMLS CUI [1,2]
C3847505
UMLS CUI [1,3]
C0449416

Similar models

The subject consent data table contains subject IDs, consent group information, and subject aliases.

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
pht008602
C3846158 (UMLS CUI [1,1])
SUBJECT_ID
Item
De-identified Subject Identifier
string
C4684638 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Item
Consent Group
text
C0021430 (UMLS CUI [1,1])
C0441833 (UMLS CUI [1,2])
Code List
Consent Group
CL Item
Disease-Specific (Arteriosclerosis and its Risk Factors, NPU) (DS-ASC-RF-NPU) (1)
SUBJECT_SOURCE
Item
Repository name for dbGaP study also containing this individual
string
C5669549 (UMLS CUI [1,1])
C0947630 (UMLS CUI [1,2])
C3846158 (UMLS CUI [1,3])
SOURCE_SUBJECT_ID
Item
Subject ID used in the SUBJECT_SOURCE repository
string
C2348585 (UMLS CUI [1,1])
C3847505 (UMLS CUI [1,2])
C0449416 (UMLS CUI [1,3])

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