Bone morphogenic protein-7 serum level decreases significantly in patients with contrast-induced nephropathy


Duranay M., Segall L., Nihat Sen S., Yilmaz F. M., Cetin M., Isleyen A., ...More

International Urology and Nephrology, vol.43, no.3, pp.807-812, 2011 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 43 Issue: 3
  • Publication Date: 2011
  • Doi Number: 10.1007/s11255-010-9871-z
  • Journal Name: International Urology and Nephrology
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.807-812
  • Keywords: Bone morphogenic protein-7, Contrast nephropathy
  • Ankara Yıldırım Beyazıt University Affiliated: Yes

Abstract

Background and Aim Previous studies have demonstrated that endogenous bone morphogenic protein- 7 (BMP-7) level is reduced in acute kidney injury and administration of exogenous BMP-7 has a beneficial effect on kidney function. In spite of preventive management, contrast-induced nephropathy (CIN) is still the third cause of acute deterioration of kidney function in hospitalized patients. With this background in mind, we studied changes in serum BMP-7 in a group of patients with chronic kidney disease and contrast-induced nephropathy. Materials and Methods We enrolled 45 consecutive adult patients with a baseline serum creatinine ≥1.4 mg/dl admitted for coronary angiography. We measured serum BMP-7 levels before and 48 h after coronary angiography. The primary end point was the development of CIN, defined as an increase in serum creatinine concentration by 0.25 mg/dl or 25% over the baseline value within 72 h from contrast exposure. Results Overall, CIN occurred in 8 (17%) patients. The concentrations of serum BMP-7 were significantly decreased in the CIN group compared to baseline (488.6 ± 56.8 vs. 356.4 ± 24.8, P = 0.01); in contrast, the concentration of BMP-7 level did not change in patients without CIN (444.6 ± 54.6 vs. 440.0 ± 53.9, P = 0.09). Conclusion BMP-7 level significantly decreases in patients who develop CIN after coronary angiography. Therefore, BMP-7 might be a diagnostic biomarker for CIN and a possibly promising agent for the treatment of CIN. © Springer Science+Business Media, B.V. 2010.