Metformin attenuates the postprandial fall in blood pressure in type 2 diabetes.
Malcolm J BorgKaren Louise JonesZilin SunMichael HorowitzChristopher K RaynerChinmay S MarathePublished in: Diabetes, obesity & metabolism (2019)
Metformin has been shown to modulate the cardiovascular response to intraduodenal glucose in patients with type 2 diabetes (T2DM), and may have the capacity to regulate postprandial blood pressure (BP), which is often inadequately compensated in T2DM, resulting in postprandial hypotension. In the present study, we evaluated the acute effects of metformin on the BP and heart rate (HR) responses to oral glucose in patients with T2DM. Ten diet-controlled T2DM patients were evaluated on two occasions in a double-blind, randomized, crossover design. Participants received either metformin 1 g or saline (control) intraduodenally 60 minutes before ingesting a 50 g glucose drink labelled with 150 mg 13 C-acetate. BP, HR, plasma glucagon-like peptide-1 (GLP-1) and gastric emptying (breath test) were evaluated over 180 minutes. Systolic and diastolic BP decreased and HR increased after oral glucose (P < 0.001 for all) on both days. Metformin attenuated the fall in systolic BP (P < 0.001), increased plasma GLP-1 concentrations (P < 0.05) and slowed gastric emptying (P < 0.05) without significantly affecting diastolic BP or HR. In conclusion, metformin acutely attenuates the hypotensive response to oral glucose, associated with augmented GLP-1 secretion and delayed gastric emptying, effects potentially relevant to its favourable cardiovascular profile.
Keyphrases
- blood pressure
- blood glucose
- heart rate
- glycemic control
- type diabetes
- hypertensive patients
- left ventricular
- heart rate variability
- end stage renal disease
- ejection fraction
- heart failure
- chronic kidney disease
- double blind
- open label
- placebo controlled
- liver failure
- weight loss
- physical activity
- newly diagnosed
- adipose tissue
- atrial fibrillation
- metabolic syndrome
- acute respiratory distress syndrome
- intensive care unit
- prognostic factors
- phase iii
- clinical trial
- respiratory failure
- patient reported