Evidence map›Paper›PMID 21378095›Full record

SynthesisHuman molecular genetics2011

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.

Ervin R Fox, J Hunter Young, Yali Li, Albert W Dreisbach, Brendan J Keating, Solomon K Musani, Kiang Liu, Alanna C Morrison, Santhi Ganesh, Abdullah Kutlar and 34 more

Open access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in Human molecular genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers, 14 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 14 pooled it
16.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

106 citing papers in PubMed, 14 syntheses or guidelines pooled it, 173 citations in OpenAlex.

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  15. Trial
  16. Variants in the neuropeptide geneAmerican journal of cancer research · 2025
    Article
  17. Review
  18. Genes, environment, and African ancestry in cardiometabolic disorders.Trends in endocrinology and metabolism: TEM · 2023
    Review
  19. Review
  20. Review

46 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

44 authors at 20 institutions in 3 countries.

Ervin R FoxDepartment of Medicine, University of Mississippi Medical Center, Jackson, MS, USA. efox@umc.edu
J Hunter Young
Yali Li
Albert W Dreisbach
Brendan J Keating
Solomon K Musani
Kiang Liu
Alanna C Morrison
Santhi Ganesh
Abdullah Kutlar
Vasan S Ramachandran
Josef F Polak
Richard R Fabsitz
Daniel L Dries
Deborah N Farlow
Susan Redline
Adebowale Adeyemo
Joel N Hirschorn
Yan V Sun
Sharon B Wyatt
Alan D Penman
Walter Palmas
Jerome I Rotter
Raymond R Townsend
Ayo P Doumatey
Bamidele O Tayo
Thomas H Mosley
Helen N Lyon
Sun J Kang
Charles N Rotimi
Richard S Cooper
Nora Franceschini
J David Curb
Lisa W Martin
Charles B Eaton
Sharon L R Kardia
Herman A Taylor
Mark J Caulfield
Georg B Ehret
Toby Johnson
International Consortium for Blood Pressure Genome-wide Association Studies (ICBP-GWAS)
Aravinda Chakravarti
Xiaofeng Zhu
Daniel Levy
Queen Mary University of London · GBLoyola University Chicago · USNational Human Genome Research Institute · USNational Institutes of Health · USPacific Health Research and Education Institute · USThe University of Texas at Austin · USBoston Children's Hospital · USCase Western Reserve University · USGeorge Washington University · USJohns Hopkins University · USNorthwestern University · USUniversity of Michigan · USUniversity of Pennsylvania · USWilliam Harvey Research Institute · GBAugusta University · USBoston University · USBroad Institute · USBrown University · USCedars-Sinai Medical Center · USColumbia University · US

Funding

Framingham Project/LevyZIAHL006001 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEVY, DANIEL · 2009 to 2025
$51.1M
Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
Research BaseP30DK072488 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI MITCHELL, BRAXTON D, TAYLOR, SIMEON I. · 2005 to 2019
$17.3M
Social-biological predictors of heterogeneity in CVD risk in African AmericansP60MD002249 · NIMHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DIEZ ROUX, ANA VICTORIA · 2007 to 2016
$15.0M
Carolina Population CenterR24HD050924 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MORGAN, SAMUEL PHILIP · 2005 to 2014
$10.0M
Genomic Predictors of Arteriosclerosis in HypertensivesR01HL087660 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KARDIA, SHARON L · 2007 to 2009
$5.1M
CHS Events Follow-up StudyU01HL080295 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M · 2005 to 2008
$4.6M
JACKSON HEART STUDY--EXAM CENTERN01HC095171 · HC · UNIVERSITY OF MISSISSIPPI MEDICAL CENTER · PI JONES, DANIEL W · 1999 to 2001
$4.6M
DATA COORDINATING CENTER FOR SLEEP HEART STUDYU01HL064360 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI DIENER-WEST, MARIE · 1999 to 2007
$4.4M
The Aging Genome Association Study "AGE-GAIN"ZIAAG000965 · NIA · NATIONAL INSTITUTE ON AGING · PI FERRUCCI, LUIGI · 2009 to 2025
$4.0M
Genetic & Functional Analyses of Hypertension Susceptibility GenesR01HL088120 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI CHANG, YEN PEI CHRISTY · 2007 to 2017
$3.9M
Statistical methods for analyzing high-throughput genotype dataR01HG003054 · NHGRI · LOYOLA UNIVERSITY CHICAGO · PI ZHU, XIAOFENG · 2005 to 2017
$3.6M
British Heart Foundation RG/07/008/23674British Heart Foundation RG/08/008/25291British Heart Foundation RG/08/014/24067Intramural NIH HHSMedical Research Council G0100222Medical Research Council G0400874Medical Research Council G0401527Medical Research Council G0600705Medical Research Council G0701863Medical Research Council G0801056Medical Research Council G0902037Medical Research Council G0902313Medical Research Council G1000143Medical Research Council G19/35Medical Research Council G8802774Medical Research Council G9521010Medical Research Council MC_QA137934Medical Research Council MC_U106179471Medical Research Council MC_U106188470Medical Research Council MC_U123092720Medical Research Council MC_U127561128Medical Research Council MC_U137686857NHGRI NIH HHS HG003054NHGRI NIH HHS R01 HG003054NHLBI NIH HHS HL074166NHLBI NIH HHS HL086694NHLBI NIH HHS HL086718NHLBI NIH HHS HL087660NHLBI NIH HHS HL100245NHLBI NIH HHS N01-HB-72982NHLBI NIH HHS N01-HB-72991NHLBI NIH HHS N01-HB-72992NHLBI 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6 · The paper itself

Abstract

The prevalence of hypertension in African Americans (AAs) is higher than in other US groups; yet, few have performed genome-wide association studies (GWASs) in AA. Among people of European descent, GWASs have identified genetic variants at 13 loci that are associated with blood pressure. It is unknown if these variants confer susceptibility in people of African ancestry. Here, we examined genome-wide and candidate gene associations with systolic blood pressure (SBP) and diastolic blood pressure (DBP) using the Candidate Gene Association Resource (CARe) consortium consisting of 8591 AAs. Genotypes included genome-wide single-nucleotide polymorphism (SNP) data utilizing the Affymetrix 6.0 array with imputation to 2.5 million HapMap SNPs and candidate gene SNP data utilizing a 50K cardiovascular gene-centric array (ITMAT-Broad-CARe [IBC] array). For Affymetrix data, the strongest signal for DBP was rs10474346 (P= 3.6 × 10(-8)) located near GPR98 and ARRDC3. For SBP, the strongest signal was rs2258119 in C21orf91 (P= 4.7 × 10(-8)). The top IBC association for SBP was rs2012318 (P= 6.4 × 10(-6)) near SLC25A42 and for DBP was rs2523586 (P= 1.3 × 10(-6)) near HLA-B. None of the top variants replicated in additional AA (n = 11 882) or European-American (n = 69 899) cohorts. We replicated previously reported European-American blood pressure SNPs in our AA samples (SH2B3, P= 0.009; TBX3-TBX5, P= 0.03; and CSK-ULK3, P= 0.0004). These genetic loci represent the best evidence of genetic influences on SBP and DBP in AAs to date. More broadly, this work supports that notion that blood pressure among AAs is a trait with genetic underpinnings but also with significant complexity.

Indexed as

Genome-Wide Association StudyPolymorphism, Single NucleotideAdultAgedBlack or African AmericanBlood PressureCohort StudiesDiastoleFemaleGenetic LociGenotypeHumansHypertensionMaleMiddle AgedPhenotype

Identifiers

PMID21378095
PMCPMC3090190
OpenAlexW2112222722

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.