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

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  • Robert A Scott
  • Audrey Y Chu
  • 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
  • Aroon Hingorani
  • John W Holloway
  • Frank B Hu
  • Bo Isomaa
  • Karen A Jameson
  • Ingegerd Johansson
  • 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
  • James B Meigs
  • Erik Ingelsson
  • Inês Barroso
  • Jose C Florez
  • Paul W Franks
  • Josée Dupuis
  • Nicholas J Wareham
  • Claudia Langenberg
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 (ß = 0.22 mmol/L [95% CI 0.13-0.31], P = 1.63 × 10(-6)). All SNPs were associated with 2-h glucose (ß = 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.
Original languageEnglish
JournalDiabetes
Volume61
Issue number5
Pages (from-to)1291-6
Number of pages6
ISSN0046-0192
DOIs
Publication statusPublished - 2012

ID: 38334757