The plasma levels of atrial natriuretic peptide and brain natriuretic peptide in type 2 diabetes treated with sodium-glucose cotransporter-2 inhibitor

Ann Endocrinol (Paris). 2020 Oct;81(5):476-481. doi: 10.1016/j.ando.2020.07.1113. Epub 2020 Aug 18.

Abstract

Purpose: The aim of this study was to determine the levels of atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) after treatment with sodium-glucose cotransporter-2 (SGLT2) inhibitor or dipeptidyl peptidase-4 (DPP4) inhibitor in patients with type-2 diabetes inadequately controlled by insulin, and to determine whether variation in ANP levels can explain favorable cardiovascular outcome.

Methods: We enrolled 56 patients, aged 18-80years, with type-2 diabetes inadequately controlled by insulin: i.e., HbA1c level 7.5-10.5% despite at least 8weeks' injectable insulin at a stable mean dose of 20-150IU daily, with or without no more than two oral antidiabetic agents.

Findings: The 56 patients were randomized between 3 treatment groups: SGLT2 inhibitor (n=18), DPP4 inhibitor (n=19) and placebo (n=19). Patients who received SGLT2 inhibitor or DPP4 inhibitor treatment all showed significantly lower HbA1c levels, fasting blood glucose (FBG) levels and systolic blood pressure at 24weeks than controls. SGLT2 inhibitor treatment decreased ANP levels, BNP levels, systolic blood pressure and weight compared with placebo. Compared to those receiving DPP4 inhibitor, patients receiving SGLT2 inhibitor showed lower HbA1c levels (7.01 vs. 7.58%; P=0.03), ANP levels (28.41 vs. 43.03 pg/mL; P=0.00) and weight (66.14 vs. 71.76 kg; P=0.04) at 24weeks after adjusting for baseline values. The SGLT2 inhibitor group showed higher sodium concentrations than the placebo and DPP4 inhibitor groups (145.89 vs. 143.89 and 144.79 mmol/L, respectively; P=0.00 and P=0.04) at 24 weeks. ANP and BNP levels did not significantly correlate with HbA1c and blood glucose levels.

Implications: These results indicated that SGLT2 inhibitors may be superior to DPP4 inhibitors in reducing risk of cardiovascular disease in diabetic patients. The major study limitation was the small number of patients per group, which should be enlarged in further research.

Keywords: Blood glucose; Diabète de type 2; Dipeptidyl peptidase-4 inhibitor; Glycémie; Inhibiteur de la dipeptidyl peptidase-4; Inhibiteur du cotransporteur-2 de sodium-glucose; Natriuretic peptide; Peptide natriurétique; Sodium-glucose cotransporter-2 inhibitor; Type 2 diabetes.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adamantane / analogs & derivatives
  • Adamantane / therapeutic use
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Atrial Natriuretic Factor / blood*
  • Benzhydryl Compounds / therapeutic use
  • Blood Glucose / drug effects
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Type 2 / blood*
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Dipeptides / therapeutic use
  • Female
  • Glucosides / therapeutic use
  • Glycated Hemoglobin / drug effects
  • Glycated Hemoglobin / metabolism
  • Humans
  • Insulin / therapeutic use
  • Male
  • Middle Aged
  • Natriuretic Peptide, Brain / blood*
  • Sodium-Glucose Transporter 2 Inhibitors / therapeutic use*
  • Treatment Outcome
  • Young Adult

Substances

  • Benzhydryl Compounds
  • Blood Glucose
  • Dipeptides
  • Glucosides
  • Glycated Hemoglobin A
  • Insulin
  • Sodium-Glucose Transporter 2 Inhibitors
  • Natriuretic Peptide, Brain
  • dapagliflozin
  • Atrial Natriuretic Factor
  • saxagliptin
  • Adamantane