Dipeptidyl peptidase-4 inhibitor, sitagliptin, improves endothelial dysfunction in association with its anti-inflammatory effects in patients with coronary artery disease and uncontrolled diabetes

Circ J. 2013;77(5):1337-44. doi: 10.1253/circj.cj-12-1168. Epub 2013 Feb 2.

Abstract

Background: Dipeptidyl peptidase 4 (DPP4) inhibitors are used for treatment of diabetes mellitus (DM). We hypothesized that sitagliptin, a DPP4-inhibitor, could improve endothelial dysfunction in DM patients with coronary artery disease (CAD).

Methods and results: The 40 patients with CAD and uncontrolled DM, aged 68.7±9.4 years (mean±standard deviation) (50% males, hemoglobin A1c [HbA1c] 7.4±1.0%) were assigned to either additional treatment with sitagliptin (50 mg/day, n=20) or aggressive conventional treatment (control, n=20) for 6 months. Endothelial function was assessed by the reactive hyperemia peripheral arterial tonometry index (RHI). The clinical characteristics at baseline were not different between the groups. After treatment, fasting blood glucose and insulin levels, and lipid profiles were not different between the groups. HbA1c levels significantly improved similarly in both groups. The percent change in RHI was greater in the sitagliptin group than in the control group (62.4±59.2% vs. 15.9±22.0%, P<0.01). Furthermore, treatment with sitagliptin resulted in a significant decrease in the high-sensitivity C-reactive protein (hsCRP) level, but no such change was noted in the control group. Linear regression analysis demonstrated a significant negative relation between changes in RHI and hsCRP, but not between RHI and HbA1c.

Conclusions: Sitagliptin significantly improved endothelial function and inflammatory state in patients with CAD and uncontrolled DM, beyond its hypoglycemic action. These findings suggest that sitagliptin has beneficial effects on the cardiovascular system in DM patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Anti-Inflammatory Agents / therapeutic use*
  • Biomarkers / blood
  • C-Reactive Protein / metabolism
  • Chi-Square Distribution
  • Coronary Artery Disease / blood
  • Coronary Artery Disease / drug therapy*
  • Coronary Artery Disease / immunology
  • Coronary Artery Disease / physiopathology
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / immunology
  • Diabetes Mellitus, Type 2 / physiopathology
  • Diabetic Angiopathies / blood
  • Diabetic Angiopathies / drug therapy*
  • Diabetic Angiopathies / immunology
  • Diabetic Angiopathies / physiopathology
  • Dipeptidyl-Peptidase IV Inhibitors / therapeutic use*
  • Endothelium, Vascular / drug effects*
  • Endothelium, Vascular / immunology
  • Endothelium, Vascular / physiopathology
  • Female
  • Glycated Hemoglobin / metabolism
  • Humans
  • Inflammation Mediators / blood
  • Linear Models
  • Logistic Models
  • Male
  • Manometry
  • Middle Aged
  • Multivariate Analysis
  • Odds Ratio
  • Peripheral Arterial Disease / blood
  • Peripheral Arterial Disease / drug therapy*
  • Peripheral Arterial Disease / immunology
  • Peripheral Arterial Disease / physiopathology
  • Pyrazines / therapeutic use*
  • Risk Factors
  • Sitagliptin Phosphate
  • Time Factors
  • Treatment Outcome
  • Triazoles / therapeutic use*

Substances

  • Anti-Inflammatory Agents
  • Biomarkers
  • Dipeptidyl-Peptidase IV Inhibitors
  • Glycated Hemoglobin A
  • Inflammation Mediators
  • Pyrazines
  • Triazoles
  • hemoglobin A1c protein, human
  • C-Reactive Protein
  • Sitagliptin Phosphate