A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

Research output: Contribution to journalJournal articleResearchpeer-review

  • Nabila Bouatia-Naji
  • Amélie Bonnefond
  • Christine Cavalcanti-Proença
  • Thomas Sparsø
  • Johan Holmkvist
  • Marion Marchand
  • Jérôme Delplanque
  • Stéphane Lobbens
  • Ghislain Rocheleau
  • Emmanuelle Durand
  • Franck De Graeve
  • Jean-Claude Chèvre
  • Knut Borch-Johnsen
  • Anna-Liisa Hartikainen
  • Aimo Ruokonen
  • Jean Tichet
  • Michel Marre
  • Jacques Weill
  • Barbara Heude
  • Maithé Tauber
  • Katleen Lemaire
  • Frans Schuit
  • Paul Elliott
  • Torben Jørgensen
  • Guillaume Charpentier
  • Samy Hadjadj
  • Stéphane Cauchi
  • Martine Vaxillaire
  • Robert Sladek
  • Sophie Visvikis-Siest
  • Beverley Balkau
  • Claire Lévy-Marchal
  • François Pattou
  • David Meyre
  • Alexandra I F Blakemore
  • Marjo-Riita Jarvelin
  • Andrew J Walley
  • Christian Dina
  • Philippe Froguel
In genome-wide association (GWA) data from 2,151 nondiabetic French subjects, we identified rs1387153, near MTNR1B (which encodes the melatonin receptor 2 (MT2)), as a modulator of fasting plasma glucose (FPG; P = 1.3 x 10(-7)). In European populations, the rs1387153 T allele is associated with increased FPG (beta = 0.06 mmol/l, P = 7.6 x 10(-29), N = 16,094), type 2 diabetes (T2D) risk (odds ratio (OR) = 1.15, 95% CI = 1.08-1.22, P = 6.3 x 10(-5), cases N = 6,332) and risk of developing hyperglycemia or diabetes over a 9-year period (hazard ratio (HR) = 1.20, 95% CI = 1.06-1.36, P = 0.005, incident cases N = 515). RT-PCR analyses confirm the presence of MT2 transcripts in neural tissues and show MT2 expression in human pancreatic islets and beta cells. Our data suggest a possible link between circadian rhythm regulation and glucose homeostasis through the melatonin signaling pathway.
Original languageEnglish
JournalNature Genetics
Volume41
Issue number1
Pages (from-to)89-94
Number of pages5
ISSN1061-4036
DOIs
Publication statusPublished - 2009

Bibliographical note

Keywords: Adaptor Proteins, Signal Transducing; Adolescent; Adult; Blood Glucose; Child; Chromosomes, Human, Pair 11; Cohort Studies; Diabetes Mellitus, Type 2; Fasting; Gene Expression Profiling; Gene Expression Regulation; Genetic Predisposition to Disease; Genome-Wide Association Study; Glucokinase; Humans; Insulin Resistance; Islets of Langerhans; Meta-Analysis as Topic; Middle Aged; Polymorphism, Single Nucleotide; RNA, Messenger; Receptor, Melatonin, MT2; Receptors, Melatonin; Reproducibility of Results

ID: 11550950