Evidence map›Paper›PMID 34706549›Full record

ArticleCirculation. Genomic and precision medicine2021

Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults.

Nels C Olson, Laura M Raffield, Anne H Moxley, Tyne W Miller-Fleming, Paul L Auer, Nora Franceschini, Debby Ngo, Timothy A Thornton, Ethan M Lange, Yun Li and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. The Association ofInternational journal of molecular sciences · 2022
    Article
  11. Review
  12. Proteomics in thrombosis research.Research and practice in thrombosis and haemostasis · 2022
    Article
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

17 authors at 9 institutions in 3 countries.

Nels C Olson *Departments of Pathology and Laboratory Medicine (N.C.O., N.A.Z.), University of Vermont, Burlington.ORCID 0000-0003-1192-9969
Laura M Raffield *Departments of Genetics (L.M.R., A.H.M., Y.L., K.L.M.), University of North Carolina, Chapel Hill.ORCID 0000-0002-7892-193X
Anne H MoxleyDepartments of Genetics (L.M.R., A.H.M., Y.L., K.L.M.), University of North Carolina, Chapel Hill.
Tyne W Miller-FlemingDivision of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN (T.W.M.-F., N.J.C.).ORCID 0000-0002-0398-5162
Paul L AuerJoseph J. Zilber School of Public Health, University of Wisconsin-Milwaukee (P.L.A.).ORCID 0000-0003-1735-8044
Nora FranceschiniEpidemiology (N.F.), University of North Carolina, Chapel Hill.ORCID 0000-0001-9755-2175
Debby NgoBeth Israel Deaconess Medical Center, Boston, MA (D.N., R.E.G.).ORCID 0000-0003-2681-3475
Timothy A ThorntonDepartments of Biostatistics (T.A.T.), University of Washington, Seattle.
Ethan M LangeDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora (E.M.L.).
Yun LiDepartments of Genetics (L.M.R., A.H.M., Y.L., K.L.M.), University of North Carolina, Chapel Hill.ORCID 0000-0002-9275-4189
Deborah A NickersonGenome Sciences (D.A.N.), University of Washington, Seattle.
Neil A ZakaiDepartments of Pathology and Laboratory Medicine (N.C.O., N.A.Z.), University of Vermont, Burlington.ORCID 0000-0001-8824-4410
Robert E GersztenBeth Israel Deaconess Medical Center, Boston, MA (D.N., R.E.G.).ORCID 0000-0002-6767-7687
Nancy J CoxDivision of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN (T.W.M.-F., N.J.C.).ORCID 0000-0001-9315-0830
Adolfo CorreaDepartment of Medicine, University of Mississippi Medical Center, Jackson (A.C.).ORCID 0000-0002-9501-600X
Karen L MohlkeDepartments of Genetics (L.M.R., A.H.M., Y.L., K.L.M.), University of North Carolina, Chapel Hill.ORCID 0000-0001-6721-153X
Alexander P ReinerEpidemiology (A.P.R.), University of Washington, Seattle.ORCID 0000-0002-1427-4470
University of North Carolina at Chapel Hill · USBeth Israel Deaconess Medical Center · USUniversity of Vermont · USUniversity of Washington · USVanderbilt University Medical Center · USHuman Genome Sciences (United States) · USJackson Memorial Hospital · USUniversity of Colorado Anschutz Medical Campus · USUniversity of Saint Joseph · CN

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
VANDERBILT UNIVERSITY CTSA FOR PEDIATRIC RESEARCHUL1RR024975 · NCRR · VANDERBILT UNIVERSITY · PI BERNARD, GORDON RAPHAEL · 2007 to 2011
$45.7M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Pharmacogenomics of Arrhythmia TherapyU19HL065962 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RODEN, DAN M · 2010 to 2014
$17.4M
Understanding and preventing HLA-associated drug reactionsP50GM115305 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DENNY, JOSHUA C. · 2015 to 2019
$13.0M
Targeted Genetic Analysis of T2D and Quantitative TraitsR01DK072193 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KAREN L. MOHLKE · 2005 to 2026
$11.3M
North Carolina Translational and Clinical Science Institute (NC TraCS) KL2KL2TR002490 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WEINBERGER, MORRIS · 2018 to 2022
$11.0M
Studies of Rare Genetic Variation in the Isolated Population of SardiniaR01HL117626 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABECASIS, GONCALO · 2013 to 2016
$10.5M
Rare variants and NHLBI traits in deeply phenotyped cohortsR01HL120393 · NHLBI · UNIVERSITY OF WASHINGTON · PI PSATY, BRUCE M, RICE, KENNETH M. · 2014 to 2016
$8.9M
The Genetic Epemiology of Multiple SclerosisR01NS032830 · NINDS · VANDERBILT UNIVERSITY · PI HAINES, JONATHAN L · 1995 to 2010
$8.9M
Epidemiologic Architecture for Genes Linked to Environment (EAGLE)U01HG004798 · NHGRI · VANDERBILT UNIVERSITY · PI CRAWFORD, DANA C · 2008 to 2013
$8.8M
VESPA: Vanderbilt Electronic Systems for Pharmacogenomic AssessmentRC2GM092618 · NIGMS · VANDERBILT UNIVERSITY · PI DENNY, JOSHUA C., RODEN, DAN M · 2009 to 2010
$6.4M
NCATS NIH HHS KL2 TR002490NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1 TR002243NCRR NIH HHS S10 RR025141NCRR NIH HHS UL1 RR024975NHGRI NIH HHS T32 HG008341NHGRI NIH HHS U01 HG004798NHGRI NIH HHS U01 HG006378NHGRI NIH HHS U01 HG011720NHLBI NIH HHS HHSN268201100037CNHLBI NIH HHS HHSN268201800001CNHLBI NIH HHS HHSN268201800010INHLBI NIH HHS HHSN268201800011CNHLBI NIH HHS HHSN268201800011INHLBI NIH HHS HHSN268201800012CNHLBI NIH HHS HHSN268201800012INHLBI NIH HHS HHSN268201800014CNHLBI NIH HHS HHSN268201800014INHLBI NIH HHS HHSN268201800015INHLBI NIH HHS R00 HL129045NHLBI NIH HHS R01 HL117626NHLBI NIH HHS R01 HL120393NHLBI NIH HHS R01 HL132947NHLBI NIH HHS T32 HL129982NHLBI NIH HHS U01 HL120393NHLBI NIH HHS U19 HL065962NICHD NIH HHS R01 HD074711NIDDK NIH HHS R01 DK072193NIDDK NIH HHS R01 DK117445NIGMS NIH HHS P50 GM115305NIGMS NIH HHS RC2 GM092618NIH HHS S10 OD017985NIMHD NIH HHS HHSN268201800013INIMHD NIH HHS R01 MD012765NINDS NIH HHS R01 NS032830
6 · The paper itself

Abstract

backgroundsuPAR (Soluble urokinase plasminogen activator receptor) has emerged as an important biomarker of coagulation, inflammation, and cardiovascular disease (CVD) risk. The contribution of suPAR to CVD risk and its genetic influence in Black populations have not been evaluated.

methodsWe measured suPAR in 3492 Black adults from the prospective, community-based JHS (Jackson Heart Study). Cross-sectional associations of suPAR with lifestyle and CVD risk factors were assessed, whole-genome sequence data were used to evaluate genetic associations of suPAR, and relationships of suPAR with incident CVD outcomes and overall mortality were estimated over follow-up.

resultsIn Cox models adjusted for traditional CVD risk factors, estimated glomerular filtration rate, and CRP (C-reactive protein), each 1-SD higher suPAR was associated with a 21% to 31% increased risk of incident coronary heart disease, heart failure, stroke, and mortality. In the genome-wide association study, 2 missense (rs399145 encoding p.Thr86Ala, rs4760 encoding p.Phe272Leu) and 2 noncoding regulatory variants (rs73935023 within an enhancer element and rs4251805 within the promoter) of

conclusionsOur results demonstrate the importance of ancestry-differentiated genetic variation on suPAR levels and indicate suPAR is a CVD biomarker in Black adults.

Indexed as

Cardiovascular DiseasesReceptors, Urokinase Plasminogen ActivatorAdultCross-Sectional StudiesGenetic VariationGenome-Wide Association StudyHumansProspective StudiesReceptors, Urokinase Plasminogen Activatorbiomarkerscardiovascular diseasesepidemiologic studiesgenome-wide association studyreceptors, urokinase plasminogen activator

Identifiers

PMID34706549
PMCPMC8692389
OpenAlexW3208658984

What Socratic holds

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Registered trials

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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 Socratic graph.