Evidence map›Paper›PMID 22415877›Full record

SynthesisDiabetes2012

No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels.

Robert A Scott, Audrey Y Chu, Niels Grarup, Alisa K Manning, Marie-France Hivert, Dmitry Shungin, Anke Tönjes, Ajay Yesupriya, Daniel Barnes, Nabila Bouatia-Naji and 97 more

Open access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Diabetes, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 6 pooled it
1.0field-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

16 citing papers in PubMed, 6 syntheses or guidelines pooled it, 27 citations in OpenAlex.

  1. Pooled it
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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

107 authors at 20 institutions in 10 countries.

Robert A ScottMedical Research Council Epidemiology Unit, Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge, UK. robert.scott@mrc-epid.cam.ac.uk
Audrey Y Chu
Niels Grarup
Alisa K Manning
Marie-France Hivert
Dmitry Shungin
Anke Tönjes
Ajay Yesupriya
Daniel Barnes
Nabila Bouatia-Naji
Nicole L Glazer
Anne U Jackson
Zoltán Kutalik
Vasiliki Lagou
Diana Marek
Laura J Rasmussen-Torvik
Heather M Stringham
Toshiko Tanaka
Mette Aadahl
Dan E Arking
Sven Bergmann
Eric Boerwinkle
Lori L Bonnycastle
Stefan R Bornstein
Eric Brunner
Suzannah J Bumpstead
Soren Brage
Olga D Carlson
Han Chen
Yii-Der Ida Chen
Peter S Chines
Francis S Collins
David J Couper
Elaine M Dennison
Nicole F Dowling
Josephine S Egan
Ulf Ekelund
Michael R Erdos
Nita G Forouhi
Caroline S Fox
Mark O Goodarzi
Jürgen Grässler
Stefan Gustafsson
Göran Hallmans
Torben Hansen
Aroon Hingorani
John W Holloway
Frank B Hu
Bo Isomaa
Karen A Jameson
Ingegerd Johansson
Anna Jonsson
Torben Jørgensen
Mika Kivimaki
Peter Kovacs
Meena Kumari
Johanna Kuusisto
Markku Laakso
Cécile Lecoeur
Claire Lévy-Marchal
Guo Li
Ruth J F Loos
Valeri Lyssenko
Michael Marmot
Pedro Marques-Vidal
Mario A Morken
Gabriele Müller
Kari E North
James S Pankow
Felicity Payne
Inga Prokopenko
Bruce M Psaty
Frida Renström
Ken Rice
Jerome I Rotter
Denis Rybin
Camilla H Sandholt
Avan A Sayer
Peter Shrader
Peter E H Schwarz
David S Siscovick
Alena Stancáková
Michael Stumvoll
Tanya M Teslovich
Gérard Waeber
Gordon H Williams
Daniel R Witte
Andrew R Wood
Weijia Xie
Michael Boehnke
Cyrus Cooper
Luigi Ferrucci
Philippe Froguel
Leif Groop
W H Linda Kao
Peter Vollenweider
Mark Walker
Richard M Watanabe
Oluf Pedersen
James B Meigs
Erik Ingelsson
Inês Barroso
Jose C Florez
Paul W Franks
Josée Dupuis
Nicholas J Wareham
Claudia Langenberg
Addenbrooke's Hospital · GBLund University · SEBoston University · USNational Institutes of Health · USUniversity College London · GBUniversity of Copenhagen · DKNational Institute on Aging · USUniversity Hospital Carl Gustav Carus · DEUniversity of Michigan · USBrigham and Women's Hospital · USCedars-Sinai Medical Center · USCentre National de la Recherche Scientifique · FRMRC Lifecourse Epidemiology Unit · GBSIB Swiss Institute of Bioinformatics · CHUniversity of Eastern Finland · FIUniversity of Washington · USCenters for Disease Control and Prevention · USCentre for Human Genetics · GBHarvard University · USIFB Adiposity Diseases · DE

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrea L Hevener · 2003 to 2026
$40.4M
Genetic analysis of type II diabetes in Finnish populationZIAHG000024 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI ERDOS, MICHAEL · 2009 to 2025
$38.2M
U OF TEXAS HLTH SCI CTR HOUSTON CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCESUL1RR024148 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2010
$27.9M
MULTIDISCIPLINARY CLINICAL AND TRANSLATIONAL SCIENCE (MCTS) PROGRAM (UL1)UL1RR025741 · NCRR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GREENLAND, PHILIP · 2008 to 2011
$24.7M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILLIAM H HERMAN · 2013 to 2026
$24.3M
University of Michigan Training Program in Genomic ScienceT32HG000040 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Sebastian Zoellner · 1995 to 2026
$16.4M
Fine-mapping and Characterization of Metabolic Loci in the DPP Outcomes StudyR01DK072041 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI FLOREZ, JOSE CARLOS · 2005 to 2017
$7.6M
Framingham Heart Study/FoxZIAHL006094 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI FOX, CAROLINE · 2010 to 2015
$6.9M
Training Program in the Epidemiology of CVDT32HL007575 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BURING, JULIE E., RIDKER, PAUL M. · 1985 to 2019
$5.0M
Epidemiology of Precursors to Type 2 DiabetesK24DK080140 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2007 to 2016
$1.9M
British Heart Foundation RG/07/008/23674Medical Research Council G0100222Medical Research Council G0600717Medical Research Council G0701863Medical Research Council G0902037Medical Research Council G1002084Medical Research Council G19/35Medical Research Council G8802774Medical Research Council MC_U106179471Medical Research Council MC_U106179473Medical Research Council MC_U147585824Medical Research Council MC_UP_A100_1003Medical Research Council MC_UP_A620_1014Medical Research Council MC_UP_A620_1015NCATS NIH HHS UL1 TR000124NCRR NIH HHS UL1 RR024148NCRR NIH HHS UL1 RR025741NHGRI NIH HHS T32 HG000040NHLBI NIH HHS T32 HL007575NIDDK NIH HHS K24 DK080140NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK063491NIDDK NIH HHS R01 DK072041
6 · The paper itself

Abstract

Gene-lifestyle interactions have been suggested to contribute to the development of type 2 diabetes. Glucose levels 2 h after a standard 75-g glucose challenge are used to diagnose diabetes and are associated with both genetic and lifestyle factors. However, whether these factors interact to determine 2-h glucose levels is unknown. We meta-analyzed single nucleotide polymorphism (SNP) × BMI and SNP × physical activity (PA) interaction regression models for five SNPs previously associated with 2-h glucose levels from up to 22 studies comprising 54,884 individuals without diabetes. PA levels were dichotomized, with individuals below the first quintile classified as inactive (20%) and the remainder as active (80%). BMI was considered a continuous trait. Inactive individuals had higher 2-h glucose levels than active individuals (β = 0.22 mmol/L [95% CI 0.13-0.31], P = 1.63 × 10(-6)). All SNPs were associated with 2-h glucose (β = 0.06-0.12 mmol/allele, P ≤ 1.53 × 10(-7)), but no significant interactions were found with PA (P > 0.18) or BMI (P ≥ 0.04). In this large study of gene-lifestyle interaction, we observed no interactions between genetic and lifestyle factors, both of which were associated with 2-h glucose. It is perhaps unlikely that top loci from genome-wide association studies will exhibit strong subgroup-specific effects, and may not, therefore, make the best candidates for the study of interactions.

Indexed as

Blood GlucoseBody Mass IndexEpigenesis, GeneticGene Expression RegulationGenotypeHumansLife StyleMotor ActivityPolymorphism, Single NucleotideBlood Glucose

Identifiers

PMID22415877
PMCPMC3331745
OpenAlexW2132085834

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.