In obese adults given liraglutide, carriers of the GLP1R rs6923761 A allele had a numerically greater delay in gastric emptying than GG carriers, but the difference was not significant (P = .11).
In plain wordsIn obese adults given liraglutide, carriers of one gene variant had a numerically longer stomach-emptying delay than others, but the difference was not statistically significant.
- Peptide
- Liraglutide
- Outcome
- No significant changeGastric emptying T1/2 delay by GLP1R rs6923761 genotype, liraglutide
- Study
n: not reported in source
- Comparator
- GG genotype
- Outcome group
- Gastrointestinal protection · Gastrointestinal
- Studied dose
- 3 mg daily · 5 weeksAs given in this study (human).
Measurements
- Gastric emptying T1/2 delay, AA/AG carriers
- 128.9 minutes
- liraglutide
- Gastric emptying T1/2 delay, GG genotype
- 61.4 minutes
- liraglutide
Source sentences
GLP1R rs6923761 minor allele A (AA_AG) carriers who received either exenatide or liraglutide had greater delay in GE T1/2 relative to baseline (117.9 ± 27.5 [SEM] minutes and 128.9 ± 38.32 minutes) compared to GG genotype (95.8 ± 30.4 minutes and 61.4 ± 21.4 minutes, respectively; P = .11).
1 context sentence(design, population, supporting numbers)
We evaluated in obese individuals the associations of genetic variations of GLP1R (rs6923761) and TCF7L2 (rs7903146) on GE T1/2 and weight from two trials that evaluated separately exenatide, 5 μg BID for 30 days, or liraglutide, 3 mg daily for 5 weeks.