Abstract
The incretin hormone glucagon-like peptide 1 (GLP-1) promotes glucose homeostasis and enhances b-cell function. GLP-1 receptor agonists (GLP-1 RAs) and dipeptidyl peptidase-4 (DPP-4) inhibitors, which inhibit the physiological inactivation of endogenous GLP-1, are used for the treatment of type 2 diabetes. Using the Metabochip, we identified three novel genetic loci with large effects (3040%) on GLP-1stimulated insulin secretion during hyperglycemic clamps in nondiabetic Caucasian individuals (TMEM114; CHST3 and CTRB1/2; n = 232; all P ≤8.8 × 10
| Original language | English |
|---|---|
| Pages (from-to) | 3275-3281 |
| Journal | Diabetes |
| Volume | 62 |
| Issue number | 9 |
| Early online date | 14 May 2013 |
| DOIs | |
| Publication status | Published - 2013 |
Cohort Studies
- Netherlands Twin Register (NTR)