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Published on: January 18, 2019
Bone morphogenic protein-7 serum level decreases significantly in patients with contrast-induced nephropathy
Murat Duranay1, Liviu Segall, Nihat Sen
1Department of Internal Medicine, Section of Nephrology, Ankara Training and Research Hospital, Ankara, Turkey.
Insights
Serum bone morphogenic protein-7 (BMP-7) levels significantly decrease in patients who develop contrast-induced nephropathy (CIN). This suggests BMP-7 may serve as a diagnostic biomarker for CIN.
Area of Science:
- Nephrology
- Biochemistry
Background:
- Endogenous bone morphogenic protein-7 (BMP-7) reduction is linked to acute kidney injury.
- Exogenous BMP-7 administration shows therapeutic potential for kidney function.
- Contrast-induced nephropathy (CIN) remains a significant cause of acute kidney injury in hospitalized patients.
Purpose of the Study:
- To investigate serum BMP-7 level changes in patients with chronic kidney disease and CIN.
- To evaluate BMP-7 as a potential biomarker for CIN development.
Main Methods:
- 45 adult patients with chronic kidney disease (serum creatinine ≥ 1.4 mg/dl) undergoing coronary angiography were enrolled.
- Serum BMP-7 levels were measured pre-procedure and 48 hours post-procedure.
- CIN was defined as a ≥0.25 mg/dl or 25% increase in serum creatinine within 72 hours.
Main Results:
- CIN developed in 8 (17%) patients.
- Patients who developed CIN showed a significant decrease in serum BMP-7 levels post-angiography (488.6 ± 56.8 to 356.4 ± 24.8, P = 0.01).
- Serum BMP-7 levels remained unchanged in patients without CIN (444.6 ± 54.6 to 440.0 ± 53.9, P = 0.09).
Conclusions:
- Serum BMP-7 levels significantly decrease in patients developing CIN after coronary angiography.
- BMP-7 may serve as a diagnostic biomarker for CIN.
- BMP-7 shows promise as a potential therapeutic agent for CIN.
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.
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