Effects of Common Genetic Variants Associated With Type 2 Diabetes and Glycemic Traits on α- and β-Cell Function and Insulin Action in Humans
- Anna Jonsson1,2⇑,
- Claes Ladenvall1,
- Tarunveer Singh Ahluwalia1,2,
- Jasmina Kravic1,
- Ulrika Krus1,
- Jalal Taneera1,
- Bo Isomaa3,4,
- Tiinamaija Tuomi3,5,
- Erik Renström1,
- Leif Groop1,6 and
- Valeriya Lyssenko1,7
- 1Department of Clinical Sciences, Diabetes and Endocrinology, Lund University Diabetes Centre, Lund University, Malmö, Sweden
- 2Novo Nordisk Foundation Centre for Basic Metabolic Research, Section of Metabolic Genetics, Faculty of Health and Medical and Sciences, University of Copenhagen, Copenhagen, Denmark
- 3Folkhälsan Research Centre, Helsinki, Finland
- 4Department of Social Services and Health Care, Jakobstad, Finland
- 5Department of Medicine, Helsinki University Central Hospital, Helsinki, Finland
- 6Finnish Institute of Molecular Medicine, Helsinki University, Helsinki, Finland
- 7Steno Diabetes Center A/S, Gentofte, Denmark
- Corresponding author: Anna Jonsson, .
Although meta-analyses of genome-wide association studies have identified >60 single nucleotide polymorphisms (SNPs) associated with type 2 diabetes and/or glycemic traits, there is little information on whether these variants also affect α-cell function. The aim of the current study was to evaluate the effects of glycemia-associated genetic loci on islet function in vivo and in vitro. We studied 43 SNPs in 4,654 normoglycemic participants from the Finnish population-based Prevalence, Prediction, and Prevention of Diabetes-Botnia (PPP-Botnia) Study. Islet function was assessed, in vivo, by measuring insulin and glucagon concentrations during oral glucose tolerance test, and, in vitro, by measuring glucose-stimulated insulin and glucagon secretion from human pancreatic islets. Carriers of risk variants in BCL11A, HHEX, ZBED3, HNF1A, IGF1, and NOTCH2 showed elevated whereas those in CRY2, IGF2BP2, TSPAN8, and KCNJ11 showed decreased fasting and/or 2-h glucagon concentrations in vivo. Variants in BCL11A, TSPAN8, and NOTCH2 affected glucagon secretion both in vivo and in vitro. The MTNR1B variant was a clear outlier in the relationship analysis between insulin secretion and action, as well as between insulin, glucose, and glucagon. Many of the genetic variants shown to be associated with type 2 diabetes or glycemic traits also exert pleiotropic in vivo and in vitro effects on islet function.
This article contains Supplementary Data online at http://diabetes.diabetesjournals.org/lookup/suppl/doi:10.2337/db12-1627/-/DC1.
- Received November 27, 2012.
- Accepted March 28, 2013.
- © 2013 by the American Diabetes Association.
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