Evidence map›Paper›PMID 30659074›Full record

ArticleDiabetes care2019

Mendelian Randomization Analysis of Hemoglobin A

Aaron Leong, Ji Chen, Eleanor Wheeler, Marie-France Hivert, Ching-Ti Liu, Jordi Merino, Josée Dupuis, E Shyong Tai, Jerome I Rotter, Jose C Florez and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes care, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
6.1field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 73 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 3 countries.

Aaron LeongMassachusetts General Hospital, Boston, MA asleong@mgh.harvard.edu.ORCID 0000-0002-3248-9547
Ji ChenWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, U.K.
Eleanor WheelerWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, U.K.
Marie-France HivertMassachusetts General Hospital, Boston, MA.ORCID 0000-0001-7752-2585
Ching-Ti LiuDepartment of Biostatistics, Boston University School of Public Health, Boston, MA.
Jordi MerinoMassachusetts General Hospital, Boston, MA.ORCID 0000-0001-8312-1438
Josée DupuisDepartment of Biostatistics, Boston University School of Public Health, Boston, MA.
E Shyong TaiDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Jerome I RotterInstitute for Translational Genomics and Population Sciences, Departments of Pediatrics and Medicine, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, CA.
Jose C FlorezMassachusetts General Hospital, Boston, MA.ORCID 0000-0002-1730-9325
Inês BarrosoWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, U.K.ORCID 0000-0001-5800-4520
James B MeigsMassachusetts General Hospital, Boston, MA.ORCID 0000-0002-2439-2657
Broad Institute · USWellcome Sanger Institute · GBBoston University · USHarvard University · USNational University of Singapore · SGThe Lundquist Institute · US

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrea L Hevener · 2003 to 2026
$40.4M
Common Genetic Variation and Quantitative Diabetes TraitsR01DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2008 to 2014
$5.0M
Rare Sequence Variation and Diabetes Quantitative TraitsU01DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2015 to 2019
$3.6M
Epidemiology of Precursors to Type 2 DiabetesK24DK080140 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2007 to 2016
$1.9M
Mentoring Investigators on the Clinical Translation of Genetic Discoveries in Type 2 DiabetesK24DK110550 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI FLOREZ, JOSE CARLOS · 2016 to 2020
$812k
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NCATS NIH HHS UL1 TR001881NIDDK NIH HHS K24 DK080140NIDDK NIH HHS K24 DK110550NIDDK NIH HHS P30 DK063491NIDDK NIH HHS R01 DK078616NIDDK NIH HHS U01 DK078616Wellcome TrustWellcome Trust WT206194
6 · The paper itself

Abstract

objectiveObservational studies show that higher hemoglobin A RESEARCH DESIGN AND

methodsTo examine the association of A1C with CAD, we selected 50 A1C-associated variants (log

resultsGenetically increased A1C was associated with higher CAD risk (odds ratio [OR] 1.61 [95% CI 1.40, 1.84] per %-unit,

conclusionsGenetic evidence supports a causal link between higher A1C and higher CAD risk. This relationship is driven not only by glycemic but also by erythrocytic, glycemia-independent factors.

Indexed as

Coronary Artery DiseaseGlycated HemoglobinAdultAgedAged, 80 and overBayes TheoremBlood GlucoseCase-Control StudiesFastingFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisMiddle AgedBlood GlucoseGlycated Hemoglobin

Identifiers

PMID30659074
PMCPMC6609962
OpenAlexW2910587421

What OpenQuestion holds

Textmetadata
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.