4.3 Article

Sitagliptin improves albuminuria in patients with type 2 diabetes mellitus

期刊

JOURNAL OF DIABETES INVESTIGATION
卷 5, 期 3, 页码 313-319

出版社

WILEY-BLACKWELL
DOI: 10.1111/jdi.12142

关键词

Albuminuria; Dipeptidyl peptidase-4 inhibitor; Sitagliptin

资金

  1. Ministry of Health, Labor and Welfare of Japan
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan
  3. Joint Research Association for Japanese Diabetes
  4. University of Occupational and Environmental Health, Japan
  5. Mitsubishi-Tanabe
  6. Eisai
  7. Chugai
  8. Abbott Japan
  9. Astellas
  10. Daiichi-Sankyo
  11. Abbvie
  12. Janssen
  13. Pfizer
  14. Takeda
  15. Astra-Zeneca
  16. Eli Lilly Japan
  17. GlaxoSmithKline
  18. Quintiles
  19. MSD
  20. Asahi-Kasei
  21. Bristol-Myers
  22. Takeda Industrial Pharma
  23. Novartis Pharma

向作者/读者索取更多资源

IntroductionThe aim of the present study was to determine the effect of sitagliptin on microalbuminuria in patients with type2 diabetes mellitus. Materials and MethodsA total of 85 patients with type2 diabetes mellitus (age >20years, <80years, hemoglobin A1c [HbA1c] <8.4%) were randomized to patients taking sitagliptin 50mg or other oral glucose-lowering agents. The following parameters were evaluated at 0, 3 and 6months after the treatment: bodyweight, blood pressure, HbA1c, fasting plasma glucose, fasting plasma insulin, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, estimated glomerular filtration rate and urinary albumin excretion. The primary outcome was changes in urinary albumin excretion at 6months. ResultsSignificant and comparable falls in HbA1c and fasting plasma glucose were found in both groups. However, sitagliptin significantly reduced urinary albumin excretion within 6months, especially in patients with high urinary albumin at baseline. A total of 27 patients with normoalbuminuria showed a reduction in urinary albumin excretion, suggesting that sitagliptin prevents the development of albuminuria. A total of 15 patients with albuminuria showed a reduction in urinary albumin excretion, suggesting the beneficial effect of sitagliptin in the early stage of diabetic nephropathy. There was a significant correlation between improvement of proteinuria and that of diastolic blood pressure. ConclusionsThe results suggested that sitagliptin improved albuminuria, in addition to improving glucose. The mechanism of the reduction of albuminuria by sitagliptin could be a direct effect, as well as an increase in active glucagon-like peptide-1, independently affecting blood pressure, bodyweight and glucose metabolism. This trial was registered with the University Hospital Medical Information Network (UMIN no. #000010871).

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