Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies.

Détails

Ressource 1Télécharger: zdc2684.pdf (166.72 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_C905D0EAEA85
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies.
Périodique
Diabetes care
Auteur(s)
Nettleton J.A., McKeown N.M., Kanoni S., Lemaitre R.N., Hivert M.F., Ngwa J., van Rooij F.J., Sonestedt E., Wojczynski M.K., Ye Z., Tanaka T., Garcia M., Anderson J.S., Follis J.L., Djousse L., Mukamal K., Papoutsakis C., Mozaffarian D., Zillikens M.C., Bandinelli S., Bennett A.J., Borecki I.B., Feitosa M.F., Ferrucci L., Forouhi N.G., Groves C.J., Hallmans G., Harris T., Hofman A., Houston D.K., Hu F.B., Johansson I., Kritchevsky S.B., Langenberg C., Launer L., Liu Y., Loos R.J., Nalls M., Orho-Melander M., Renstrom F., Rice K., Riserus U., Rolandsson O., Rotter J.I., Saylor G., Sijbrands E.J., Sjogren P., Smith A., Steingrímsdóttir L., Uitterlinden A.G., Wareham N.J., Prokopenko I., Pankow J.S., van Duijn C.M., Florez J.C., Witteman J.C., Dupuis J., Dedoussis G.V., Ordovas J.M., Ingelsson E., Cupples L., Siscovick D.S., Franks P.W., Meigs J.B.
Collaborateur(s)
MAGIC Investigators
Contributeur(s)
Dupuis J., Claudia L., Prokopenko I., Saxena R., Soranzo N., Jackson A.U., Wheeler E., Glazer N.L., Bouatia-Naji N., Lindgren C.M., Mägi R., Morris A.P., Randal J., Rybin D., Johnson T., Henneman P., Gieger C., Thorleifsson G., Steinthorsdottir V., Dehghan A., Hottenga J.J., Franklin C.S., Navarro P., Song K., Goe A., Perry J.R., Lajunen T., Grallert H., Li M., Stringham H.M., Kumari M., Timpson N.J., Shrader P., Ingelsson E., Zabena C., O'Connell J., Cavalcanti-Proença C., Luan J., Elliott A., McCarroll S.A., Payne F., Roccasecca R.M., Sethupathy P., Andrew T., Ariyurek Y., Balkau B., Barter P., Bennett A.J., Ben-Shlomo Y., Bergmann S., Bochud M., Boerwinkle E., Bonnefond A., Bonnycastle L.L., Böttcher Y., Brunner E., Bumpstead S.J., Chen Y.D., Chines P., Clarke R., Coin L.J., Crawford G.J., Crisponi L., Day I.N., Geus Ed, Dina C., Doney A., Egan J.M., Elliott P., Erdos M.R., Fischer-Rosinsky A., Forouhi N.G., Fox C.S., Frants R., Franzosi M.G., Galan P., Goodarzi M.O., Graessler J., Groves C.J., Grundy S., Gwilliam R., Hallmans G., Hammond N., Han X., Hartikainen A.L., Hayward C., Heath S.C., Hercberg S., Herder C., Hicks A.A., Hingorani A.D., Hofman A., Isomaa B., Jula A., Kaakinen M., Kanoni S., Kesaniemi Y.A., Kivimaki M., Knight B., Koskinen S., Kovacs P., Lathrop G.M., Lawlor D.A., Li Y., Lyssenko V., Mahley R., Mangino M., Manning A.K., Martínez-Larrad M.T., McAteer J.B., McPherson R., Meisinger C., Melzer D., Meyre D., Mitchell B.D., Morken M.A., Naitza S., Narisu N., Neville M.J., Oostra B.A., Orrù M., Pakyz R., Palmer C.N., Paolisso G., Pattaro C., Pearson D., Peden J.F., Perola M., Pfeiffer A.F., Pichler I., Polasek O., Posthuma D., Potter S.C., Pouta A., Psaty B.M., Rathmann W., Rayner N.W., Rice K., Ripatti S., Rivadeneira F., Rolandsson O., Sandhu M., Sanna S., Sayer A.A., Scheet P., Scott L.J., Seedorf U., Sharp S.J., Shields B., Sijbrands E.J., Silveira A., Singleton A., Smith N.L., Sovio U., Swift A., Syddall H., Syvänen A.C., Tanaka T., Tönjes A., Tuomi T., Uitterlinden A.G., van Dijk K.W., Varma D., Visvikis-Siest S., Vitart V., Vogelzangs N., Waeber G., Wagner P.J., Watkins H., Weedon M.N., Wild S.H., Willemsen G., Witteman J.C., Yarnell J.W., Zelenika D., Zethelius B., Zhai G., Zhao J.H., Zillikens M.C., GIANT Consortium X., Global BPgen Consortium X., Loos R.J., Meneton P., Nathan D.M., Williams G.H., Hattersley A.T., Silander K., Salomaa V., Smith G.D., Bornstein S.R., Schwarz P., Spranger J., Karpe F., Shuldiner A.R., Cooper C., Dedoussis G.V., Serrano-Ríos M., Morris A.D., Lind L., Franks P.W., Ebrahim S., Marmot M., Kuusisto J., Laakso M., Kao W.H., Pankow J.S., Pramstaller P.P., Wichmann H.E., Illig T., Rudan I., Wright A., Stumvoll M., Campbell H., Wilson J.F., Hamsten A., Bergman R.N., Buchanan T.A., Collins F.S., Mohlke K.L., Tuomilehto J., Valle T.T., Altshuler D., Rotter J.I., Siscovick D.S., Penninx B.W., Boomsma D., Deloukas P., Spector T.D., Frayling T.M., Ferrucci L., Kong A., Thorsteinsdottir U., Stefansson K., van Duijn C.M., Aulchenko Y.S., Cao A., Scuteri A., Schlessinger D., Uda M., Ruokonen A., Jarvelin M.R., Waterworth D.M., Vollenweider P., Peltonen L., Mooser V., Abecasis G.R., Wareham N.J., Sladek R., Froguel P., Watanabe R.M., Meigs J.B., Groop L., Boehnke M., McCarthy M.I., Florez J.C., Barroso I.
ISSN
1935-5548 (Electronic)
ISSN-L
0149-5992
Statut éditorial
Publié
Date de publication
12/2010
Peer-reviewed
Oui
Volume
33
Numéro
12
Pages
2684-2691
Langue
anglais
Notes
Publication types: Journal Article ; Meta-Analysis Publication Status: ppublish

Résumé
Whole-grain foods are touted for multiple health benefits, including enhancing insulin sensitivity and reducing type 2 diabetes risk. Recent genome-wide association studies (GWAS) have identified several single nucleotide polymorphisms (SNPs) associated with fasting glucose and insulin concentrations in individuals free of diabetes. We tested the hypothesis that whole-grain food intake and genetic variation interact to influence concentrations of fasting glucose and insulin.
Via meta-analysis of data from 14 cohorts comprising ∼ 48,000 participants of European descent, we studied interactions of whole-grain intake with loci previously associated in GWAS with fasting glucose (16 loci) and/or insulin (2 loci) concentrations. For tests of interaction, we considered a P value <0.0028 (0.05 of 18 tests) as statistically significant.
Greater whole-grain food intake was associated with lower fasting glucose and insulin concentrations independent of demographics, other dietary and lifestyle factors, and BMI (β [95% CI] per 1-serving-greater whole-grain intake: -0.009 mmol/l glucose [-0.013 to -0.005], P < 0.0001 and -0.011 pmol/l [ln] insulin [-0.015 to -0.007], P = 0.0003). No interactions met our multiple testing-adjusted statistical significance threshold. The strongest SNP interaction with whole-grain intake was rs780094 (GCKR) for fasting insulin (P = 0.006), where greater whole-grain intake was associated with a smaller reduction in fasting insulin concentrations in those with the insulin-raising allele.
Our results support the favorable association of whole-grain intake with fasting glucose and insulin and suggest a potential interaction between variation in GCKR and whole-grain intake in influencing fasting insulin concentrations.

Mots-clé
Adult, Aged, Blood Glucose/genetics, Blood Glucose/metabolism, Edible Grain, European Continental Ancestry Group, Fasting/blood, Female, Genetic Loci/genetics, Genome-Wide Association Study, Genotype, Humans, Insulin/blood, Insulin/genetics, Male, Middle Aged, Polymorphism, Single Nucleotide/genetics
Pubmed
Création de la notice
02/10/2014 12:54
Dernière modification de la notice
20/08/2019 16:44
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