4.7 Article

Effects of intravenous exenatide in type 2 diabetic patients with congestive heart failure: a double-blind, randomised controlled clinical trial of efficacy and safety

期刊

DIABETOLOGIA
卷 55, 期 4, 页码 926-935

出版社

SPRINGER
DOI: 10.1007/s00125-011-2440-x

关键词

Congestive heart failure; Double-blind randomised trial; Exenatide; GLP-1; Heart catheterisation; Type 2 diabetes

资金

  1. Stockholm County Council
  2. Karolinska Institute
  3. Swedish Society for Medical Research
  4. Swedish Society of Medicine
  5. Stiftelsen Serafimerlasarettet
  6. Swedish Heart and Lung foundation
  7. Eli Lilly Amylin Alliance
  8. European Foundation for the Study of Diabetes
  9. Karolinska Institutet Foundations
  10. Stiftelsen Olle Engkvist Byggm stare
  11. Merck
  12. Eli Lilly
  13. Novo Nordisk
  14. sanofi-aventis
  15. Boehringer-Ingelheim
  16. AstraZeneca
  17. Novartis

向作者/读者索取更多资源

The aim of this study was to determine whether exenatide improves haemodynamic function in patients with type 2 diabetes with congestive heart failure (CHF). The main eligibility criteria for inclusion were: male/female (18-80 years) with type 2 diabetes and CHF (ejection fraction a parts per thousand currency sign35%, and New York Heart Association functional class III or IV). Out of 237 patients screened, 20 male type 2 diabetic patients participated in this crossover trial design and were allocated (sequentially numbered) to i.v. infusions during two consecutive days with (1) exenatide (0.12 pmol/kg/min); and (2) placebo for 6 h followed by a washout period for 18 h, at Stockholm South Hospital, Sweden. Patients and researchers were blinded to the assignment. Cardiac haemodynamic variables were determined by right heart catheterisation. The primary endpoint was defined as an increase in cardiac index (CI) or a decrease in pulmonary capillary wedge pressure (PCWP) of a parts per thousand yen20%. Secondary endpoints were tolerability and safety of exenatide infusion. CI increased at 3 and 6 h by 0.4 +/- 0.1 (23%) and 0.33 +/- 0.1 (17%) l min(-1) m(-2), during exenatide infusion vs -0.02 +/- 0.1 (-1%) and -0.08 +/- 0.1 (-5%) l min(-1) m(-2) during placebo (p = 0.003); and heart rate (HR) increased at 1, 3 and 6 h by 8 +/- 3 (11%), 15 +/- 4 (21%) and 21 +/- 5 (29%) beats per min (bpm), during exenatide infusion vs -1 +/- 2 (-2%), 1 +/- 1 (2%) and 6 +/- 2 (8%) bpm, during placebo (p = 0.006); and PCWP decreased at 1, 3 and 6 h by -1.3 +/- 0.8 (-8%), -1.2 +/- 1 (-8%) and -2.2 +/- 0.9 (-15%) mmHg, during exenatide infusion vs 0.3 +/- 0.5 (2%), 1 +/- 0.6 (6%) and 1.4 +/- 0.7 (8%) mmHg, during placebo (p = 0.001). No serious adverse event was observed. Adverse events were reported in nine patients (six, nausea; two, increased HR; one, increased systolic blood pressure). Infusion of exenatide in male type 2 diabetic patients with CHF increased the CI as a result of chronotropy, with concomitant favourable effects on PCWP and reasonable tolerability of the drug. The clinical implications of using exenatide in patients with CHF are still not clear and further studies are warranted.

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