Evidence map›Paper›PMID 33321069›Full record

ArticleCirculation. Genomic and precision medicine2020

Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus.

Natalie R van Zuydam, Claes Ladenvall, Benjamin F Voight, Rona J Strawbridge, Juan Fernandez-Tajes, N William Rayner, Neil R Robertson, Anubha Mahajan, Efthymia Vlachopoulou, Anuj Goel and 48 more

Open access · hybridAbstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

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

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Genome-Wide Association Study of Peripheral Artery Disease.Circulation. Genomic and precision medicine · 2021
    Article
  7. Review
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

58 authors at 20 institutions in 17 countries.

Natalie R van ZuydamPat Macpherson Center for Pharmacogenetics & Pharmacogenomics, Cardiovascular & Diabetes Medicine (N.R.v.Z., C.N.A.P.), School of Medicine, University of Dundee.
Claes LadenvallDepartment of Clinical Sciences, Diabetes & Endocrinology, Lund University Diabetes Center, Malmö, Sweden (C.L., L.G.).
Benjamin F VoightDepartment of Systems Pharmacology & Translational Therapeutics (B.F.V.).
Rona J StrawbridgeCardiovascular Medicine Unit, Department of Medicine Solna, Center for Molecular Medicine, Karolinska Institutet, Karolinska University Hospital Solna, Stockholm, Sweden (R.J.S., A.H.).
Juan Fernandez-TajesWellcome Center for Human Genetics (N.R.v.Z., J.F.T., N.W.R., N.R.R, A. Mahajan, A.G., H.W., A.P.M., M.I.Mc), University of Oxford, United Kingdom.
N William RaynerOxford Center for Diabetes, Endocrinology & Metabolism, Radcliffe Department of Medicine (N.R.v.Z., N.W.R., N.R.R., A. Mahajan, M.I.Mc), University of Oxford, United Kingdom.
Neil R RobertsonOxford Center for Diabetes, Endocrinology & Metabolism, Radcliffe Department of Medicine (N.R.v.Z., N.W.R., N.R.R., A. Mahajan, M.I.Mc), University of Oxford, United Kingdom.
Anubha MahajanOxford Center for Diabetes, Endocrinology & Metabolism, Radcliffe Department of Medicine (N.R.v.Z., N.W.R., N.R.R., A. Mahajan, M.I.Mc), University of Oxford, United Kingdom.
Efthymia VlachopoulouTransplantation Laboratory, Haartman Institute (E.V.), University of Helsinki, Helsinki, Finland.
Anuj GoelWellcome Center for Human Genetics (N.R.v.Z., J.F.T., N.W.R., N.R.R, A. Mahajan, A.G., H.W., A.P.M., M.I.Mc), University of Oxford, United Kingdom.
Marcus E Kleber
Christopher P NelsonDepartment of Cardiovascular Sciences, University of Leicester (C.P.N., N.J.S.).
Lydia Coulter KweeDuke Molecular Physiology Institute, Duke University, Durham, NC (L.C.K., S.H.S.).
Tõnu EskoEstonian Genome Center (T.E., E.M., R.M., L.M., K.F., M.P., A. Metspalu), University of Tartu, Tartu, Estonia.
Evelin MihailovEstonian Genome Center (T.E., E.M., R.M., L.M., K.F., M.P., A. Metspalu), University of Tartu, Tartu, Estonia.
Reedik MägiEstonian Genome Center (T.E., E.M., R.M., L.M., K.F., M.P., A. Metspalu), University of Tartu, Tartu, Estonia.
Lili MilaniEstonian Genome Center (T.E., E.M., R.M., L.M., K.F., M.P., A. Metspalu), University of Tartu, Tartu, Estonia.
Krista FischerEstonian Genome Center (T.E., E.M., R.M., L.M., K.F., M.P., A. Metspalu), University of Tartu, Tartu, Estonia.
Stavroula KanoniCenter for Genomic Health (S.K.), Queen Mary University of London, London, United Kingdom.
Jitender KumarDepartment of Medical Sciences, Molecular Epidemiology & Science for Life Laboratory (J.K., C.S., E.I.).
Ci SongDepartment of Medical Sciences, Molecular Epidemiology & Science for Life Laboratory (J.K., C.S., E.I.).
Jaana A HartialaDepartment of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA (J.A.H.).
Nancy L PedersenDepartment of Medical Epidemiology & Biostatistics, Karolinska Institutet, Stockholm, Sweden (N.L.P.).
Markus PerolaResearch Program for Clinical & Molecular Metabolism, Faculty of Medicine (M.P.), University of Helsinki, Helsinki, Finland. Vth Department of Medicine (Nephrology, Hypertensiology, Rheumatology, Endocrinology, Diabetology), Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Christian GiegerGerman Center for Diabetes Research (DZD), München-Neuherberg (C.G., A.P., H.G.).
Annette PetersGerman Center for Diabetes Research (DZD), München-Neuherberg (C.G., A.P., H.G.).
Liming QuCardiovascular Institute, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA (L.Q., M.P.R.).
Sara M WillemsDepartment of Epidemiology, Erasmus Medical Center, Rotterdam, the Netherlands (S.M.W., C.v.D.).
Alex S F DoneyDivision of Molecular & Clinical Medicine (A.S.F.D.), School of Medicine, University of Dundee.
Andrew D MorrisThe Usher Institute of Population Health Sciences & Informatics (A.D.M.), University of Edinburgh, Edinburgh, U.K.
Yan ZhengDepartment of Nutrition (Y.Z., F.B.H., L.Q.).
Giorgio SestiUniversity "Magna Graecia" of Catanzaro, Italy (G.S.).
Frank B HuDepartment of Nutrition (Y.Z., F.B.H., L.Q.).
Lu QiCardiovascular Institute, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA (L.Q., M.P.R.).
Markku LaaksoFaculty of Health Sciences, Institute of Clinical Medicine, Internal Medicine, University of Eastern Finland (M.L.).
Unnur ThorsteinsdottirFaculty of Medicine, University of Iceland. deCODE Genetics, Reykjavik, Iceland (U.T.).
Harald GrallertGerman Center for Diabetes Research (DZD), München-Neuherberg (C.G., A.P., H.G.).
Cornelia van DuijnDepartment of Epidemiology, Erasmus Medical Center, Rotterdam, the Netherlands (S.M.W., C.v.D.).
Muredach P ReillyCardiovascular Institute, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA (L.Q., M.P.R.).
Erik IngelssonDepartment of Medical Sciences, Molecular Epidemiology & Science for Life Laboratory (J.K., C.S., E.I.).
Panos DeloukasWilliam Harvey Research Institute, Barts & the London Medical School (S.K., P.D.), Queen Mary University of London, London, United Kingdom.
Sek KathiresanCenter for Genomic Health (S.K.), Queen Mary University of London, London, United Kingdom.
Andres MetspaluEstonian Genome Center (T.E., E.M., R.M., L.M., K.F., M.P., A. Metspalu), University of Tartu, Tartu, Estonia.
Svati H ShahDivision of Cardiology, Department of Medicine, Duke University Medical Center (S.H.S.).
Juha SinisaloHeart & Lung Center, Helsinki University Hospital (J.S.) and Institute for Molecular Medicine Finland (FIMM), Helsinki University, Helsinki, Finland.
Veikko SalomaaNational Institute for Health and Welfare, Helsinki, Finland (M.P., V.S.).
Anders HamstenCardiovascular Medicine Unit, Department of Medicine Solna, Center for Molecular Medicine, Karolinska Institutet, Karolinska University Hospital Solna, Stockholm, Sweden (R.J.S., A.H.).
Nilesh J SamaniDepartment of Cardiovascular Sciences, University of Leicester (C.P.N., N.J.S.).
Winfried MärzSynlab Academy, Synlab Holding Deutschland GmbH, Mannheim, Germany (W.M.).
Stanley L HazenLerner Research Institute, Heart & Vascular Institute, Cleveland Clinic, Cleveland, OH (S.L.H.).
Hugh WatkinsWellcome Center for Human Genetics (N.R.v.Z., J.F.T., N.W.R., N.R.R, A. Mahajan, A.G., H.W., A.P.M., M.I.Mc), University of Oxford, United Kingdom.
Danish SaleheenDepartment of Biostatistics & Epidemiology, University of Pennsylvania, Philadelphia, PA (D.S.).
Andrew P MorrisWellcome Center for Human Genetics (N.R.v.Z., J.F.T., N.W.R., N.R.R, A. Mahajan, A.G., H.W., A.P.M., M.I.Mc), University of Oxford, United Kingdom.
Helen M ColhounMRC Institute of Genetics & Molecular Medicine (H.M.C.), University of Edinburgh, Edinburgh, U.K.
Leif GroopDepartment of Clinical Sciences, Diabetes & Endocrinology, Lund University Diabetes Center, Malmö, Sweden (C.L., L.G.).
Mark I McCarthyOxford Center for Diabetes, Endocrinology & Metabolism, Radcliffe Department of Medicine (N.R.v.Z., N.W.R., N.R.R., A. Mahajan, M.I.Mc), University of Oxford, United Kingdom.
Colin N A PalmerPat Macpherson Center for Pharmacogenetics & Pharmacogenomics, Cardiovascular & Diabetes Medicine (N.R.v.Z., C.N.A.P.), School of Medicine, University of Dundee.
SUMMIT Steering Committee; CARDIOGRAMplusC4D Steering Committee*
Centre for Human Genetics · GBUniversity of Tartu · EEOxford Centre for Diabetes, Endocrinology and Metabolism · GBHelmholtz Zentrum München · DELund University · SETulane University · USBroad Institute · USDuke University · USErasmus MC · NLKarolinska University Hospital · SENHS Fife · GBUniversity of Leicester · GBAmity University · INBrigham and Women's Hospital · USCardiovascular Institute of the South · USCenter for Non-Communicable Diseases · PKCleveland Clinic Lerner College of Medicine · USdeCODE Genetics (Iceland) · ISFinnish Institute for Health and Welfare · FIFudan University · CN

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI GREENBERG, ANDREW S, PERISSI, VALENTINA · 1992 to 2021
$25.0M
Gut Flora Metabolism of Dietary Phosphatidylcholine and CVDR01HL103866 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI HAZEN, STANLEY L · 2010 to 2023
$10.8M
Algorithms to identify non-coding mutational burden and disease-relevant pathwaysR01DK101478 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI VOIGHT, BENJAMIN FRANKLIN · 2014 to 2018
$2.9M
Interstitial Cystitis in Swedish TwinsU01DK066134 · NIDDK · KAROLINSKA INSTITUTE · PI PEDERSEN, NANCY L · 2004 to 2008
$2.9M
Beyond GWAS of insulin resistance: An integrated approach to translate genetic association to functionR01DK106236 · NIDDK · STANFORD UNIVERSITY · PI KNOWLES, JOSHUA WILEY · 2016 to 2020
$2.4M
Integrating genome-scale data to reveal causal mechanisms in type 2 diabetesU01DK105535 · NIDDK · UNIVERSITY OF OXFORD · PI GLOYN, ANNA LOUISE · 2015 to 2019
$1.7M
Algorithms to identify non-coding mutational burden and disease-relevant pathwaysR56DK101478 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI VOIGHT, BENJAMIN FRANKLIN · 2019 to 2019
$272k
British Heart Foundation RG/14/5/30893Medical Research Council MC_PC_13040NHLBI NIH HHS R01 HL103866NIDDK NIH HHS P30 DK046200NIDDK NIH HHS R01 DK101478NIDDK NIH HHS R01 DK106236NIDDK NIH HHS R56 DK101478NIDDK NIH HHS U01 DK066134NIDDK NIH HHS U01 DK105535Wellcome Trust 212945/Z/18/Z
6 · The paper itself

Abstract

backgroundCoronary artery disease (CAD) is accelerated in subjects with type 2 diabetes mellitus (T2D).

methodsTo test whether this reflects differential genetic influences on CAD risk in subjects with T2D, we performed a systematic assessment of genetic overlap between CAD and T2D in 66 643 subjects (27 708 with CAD and 24 259 with T2D). Variants showing apparent association with CAD in stratified analyses or evidence of interaction were evaluated in a further 117 787 subjects (16 694 with CAD and 11 537 with T2D).

resultsNone of the previously characterized CAD loci was found to have specific effects on CAD in T2D individuals, and a genome-wide interaction analysis found no new variants for CAD that could be considered T2D specific. When we considered the overall genetic correlations between CAD and its risk factors, we found no substantial differences in these relationships by T2D background.

conclusionsThis study found no evidence that the genetic architecture of CAD differs in those with T2D compared with those without T2D.

Indexed as

Genetic Predisposition to DiseaseCase-Control StudiesCoronary Artery DiseaseDiabetes Mellitus, Type 2Genome-Wide Association StudyHumansMeta-Analysis as TopicPolymorphism, GeneticRisk Factorsblood pressurecoronary artery diseasediabetes mellitusgenome-wide association studyrisk factors

Identifiers

PMID33321069
PMCPMC7748049
OpenAlexW3049150590

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.