Evidence map›Paper›PMID 32340472›Full record

ArticleCirculation. Genomic and precision medicine2020

Genetically Determined Birthweight Associates With Atrial Fibrillation: A Mendelian Randomization Study.

Rachel L Kember, Michael G Levin, Diana L Cousminer, Noah Tsao, Renae Judy, Gayatri M Schur, Steven A Lubitz, Patrick T Ellinor, Shana E McCormack, Struan F A Grant and 4 more

Open access · bronzeAbstract 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Epigenetic Modifications at the Center of the Barker Hypothesis and Their Transgenerational Implications.International journal of environmental research and public health · 2021
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Rachel L Kember *From the Departments of Genetics (R.L.K., D.L.C., S.F.A.G., D.J.R., B.F.V.), University of Pennsylvania.
Michael G Levin *Medicine (M.G.L., D.J.R.), University of Pennsylvania.
Diana L CousminerFrom the Departments of Genetics (R.L.K., D.L.C., S.F.A.G., D.J.R., B.F.V.), University of Pennsylvania.
Noah TsaoSurgery (N.T., R.J., S.M.D.), University of Pennsylvania.
Renae JudySurgery (N.T., R.J., S.M.D.), University of Pennsylvania.
Gayatri M SchurPediatrics (G.M.S., S.E.M., S.F.A.G.), University of Pennsylvania.
Steven A LubitzCardiac Arrhythmia Service, Massachusetts General Hospital, Boston (S.A.L., P.T.E.).
Patrick T EllinorCardiac Arrhythmia Service, Massachusetts General Hospital, Boston (S.A.L., P.T.E.).
Shana E McCormackPediatrics (G.M.S., S.E.M., S.F.A.G.), University of Pennsylvania.
Struan F A GrantFrom the Departments of Genetics (R.L.K., D.L.C., S.F.A.G., D.J.R., B.F.V.), University of Pennsylvania.
Regeneron Genetics Center
Daniel J RaderFrom the Departments of Genetics (R.L.K., D.L.C., S.F.A.G., D.J.R., B.F.V.), University of Pennsylvania.
Benjamin F VoightFrom the Departments of Genetics (R.L.K., D.L.C., S.F.A.G., D.J.R., B.F.V.), University of Pennsylvania.
Scott M DamrauerSurgery (N.T., R.J., S.M.D.), University of Pennsylvania.
University of Pennsylvania · USChildren's Hospital of Philadelphia · USMassachusetts General Hospital · USPhiladelphia VA Medical Center · US

Funding

FRAMINGHAM HEART STUDY - YEAR 5 EXAM75N92019D00031 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · 2019 to 2024
$29.8M
IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVALR01HL092577 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2009 to 2025
$20.6M
Predoctoral Training Program in Human GeneticsT32GM007814 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID · 1985 to 2021
$10.6M
Genomics of Cardiac ArrhythmiasR01HL139731 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2018 to 2022
$3.3M
AFGen Consortium: Atrial Fibrillation Genomics to Functional AnalysesR01HL128914 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2015 to 2018
$3.1M
Algorithms to identify non-coding mutational burden and disease-relevant pathwaysR01DK101478 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI VOIGHT, BENJAMIN FRANKLIN · 2014 to 2018
$2.9M
Genomics of Cardiac Electrical Activity and ArrhythmiaR01HL116747 · NHLBI · UNIVERSITY OF WASHINGTON · PI ARKING, DAN E, SOTOODEHNIA, NONA · 2013 to 2016
$2.8M
Genomics of Sudden Cardiac Arrest Among African AmericansR01HL111089 · NHLBI · UNIVERSITY OF WASHINGTON · PI SOTOODEHNIA, NONA · 2012 to 2015
$2.6M
Mentoring in Arrhythmia ResearchK24HL105780 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2011 to 2020
$1.2M
Mentoring in patient-oriented atrial fibrillation and cardiovascular researchK24HL148521 · NHLBI · EMORY UNIVERSITY · PI ALONSO, ALVARO · 2019 to 2023
$593k
Algorithms to identify non-coding mutational burden and disease-relevant pathwaysR56DK101478 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI VOIGHT, BENJAMIN FRANKLIN · 2019 to 2019
$272k
Precision Cardio-Metabolic Phenotyping for Genetic Discovery and Risk PredictionIK2CX001780 · VA · PHILADELPHIA VA MEDICAL CENTER · PI DAMRAUER, SCOTT MICHAEL · 2018 to 2023
–
CSRD VA IK2 CX001780Medical Research Council MR/N025083/1NHLBI NIH HHS 75N92019D00031NHLBI NIH HHS K24 HL105780NHLBI NIH HHS K24 HL148521NHLBI NIH HHS R01 HL092577NHLBI NIH HHS R01 HL111089NHLBI NIH HHS R01 HL116747NHLBI NIH HHS R01 HL128914NHLBI NIH HHS R01 HL139731NIDDK NIH HHS R01 DK101478NIDDK NIH HHS R56 DK101478NIGMS NIH HHS T32 GM007814
6 · The paper itself

Abstract

backgroundAtrial fibrillation is a common cardiovascular disorder, characterized by irregular electrical activity in the upper chambers of the heart. Both chronic cardiometabolic risk factors and genetics have been shown to contribute to the development of atrial fibrillation. Birthweight has also been associated with risk of atrial fibrillation.

methodsIn the current study, we utilized a genetic approach to study the effect of birthweight on atrial fibrillation. We used 2-sample Mendelian randomization to consider the impact of birthweight on incident atrial fibrillation using summary data from the Early Growth Genetics Consortium GWAS of birthweight and a large biobank-based GWAS of atrial fibrillation.

resultsUsing the framework of 2-sample Mendelian randomization, we found that a 1-SD genetic elevation of birthweight was associated with increased risk of atrial fibrillation (odds ratio, 1.27 [95% CI, 1.14-1.41];

conclusionsOur findings clarify the directionality of the relationship between birthweight and atrial fibrillation, supporting the growing body of evidence that intrauterine growth has a lifelong impact on cardiovascular health.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAtrial FibrillationBirth WeightFemaleGenome-Wide Association StudyHumansMaleMendelian Randomization Analysisatrial fibrillationgeneticsheart failurehypertensionprevalence

Identifiers

PMID32340472
PMCPMC7299774
OpenAlexW3018139278

What OpenQuestion holds

Textmetadata
LicenceTDM
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.