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


Autoria(s): Scott R.A.; Chu A.Y.; Grarup N.; Manning A.K.; Hivert M.F.; Shungin D.; Tönjes A.; Yesupriya A.; Barnes D.; Bouatia-Naji N.; Glazer N.L.; Jackson A.U.; Kutalik Z.; Lagou V.; Marek D.; Rasmussen-Torvik L.J.; Stringham H.M.; Tanaka T.; Aadahl M.; Arking D.E.; Bergmann S.; Boerwinkle E.; Bonnycastle L.L.; Bornstein S.R.; Brunner E.; Bumpstead S.J.; Brage S.; Carlson O.D.; Chen H.; Chen Y.D.; Chines P.S.; Collins F.S.; Couper D.J.; Dennison E.M.; Dowling N.F.; Egan J.S.; Ekelund U.; Erdos M.R.; Forouhi N.G.; Fox C.S.; Goodarzi M.O.; Grässler J.; Gustafsson S.; Hallmans G.; Hansen T.; Hingorani A.; Holloway J.W.; Hu F.B.; Isomaa B.; Jameson K.A.; Johansson I.; Jonsson A.; Jørgensen T.; Kivimaki M.; Kovacs P.; Kumari M.; Kuusisto J.; Laakso M.; Lecoeur C.; Lévy-Marchal C.; Li G.; Loos R.J.; Lyssenko V.; Marmot M.; Marques-Vidal P.; Morken M.A.; Müller G.; North K.E.; Pankow J.S.; Payne F.; Prokopenko I.; Psaty B.M.; Renström F.; Rice K.; Rotter J.I.; Rybin D.; Sandholt C.H.; Sayer A.A.; Shrader P.; Schwarz P.E.; Siscovick D.S.; Stancáková A.; Stumvoll M.; Teslovich T.M.; Waeber G.; Williams G.H.; Witte D.R.; Wood A.R.; Xie W.; Boehnke M.; Cooper C.; Ferrucci L.; Froguel P.; Groop L.; Kao W.H.; Vollenweider P.; Walker M.; Watanabe R.M.; Pedersen O.; Meigs J.B.; Ingelsson E.; Barroso I.; Florez J.C.; Franks P.W.; Dupuis J.; Wareham N.J.; Langenberg C.
Data(s)

2012

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_E019BF6B6966

isbn:1939-327X (Electronic)

doi:10.2337/db11-0973

isiid:000303179100042

pmid:22415877

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

Diabetes, vol. 61, no. 5, pp. 1291-1296

Palavras-Chave #Blood Glucose/genetics; Blood Glucose/metabolism; Body Mass Index; Epigenesis, Genetic; Gene Expression Regulation/physiology; Genotype; Humans; Life Style; Motor Activity/physiology; Polymorphism, Single Nucleotide
Tipo

info:eu-repo/semantics/article

article