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Updated: Oct 9, 2025

Intravascular Delivery of Biologics to the Rat Kidney
Published on: September 1, 2016
Pathologic Correlation with Renal Dysfunction after Intravitreal Injections of Vascular Endothelial Growth Factor
Ping L Zhang1, Shazia Raza2, Wei Li3
1Division of Anatomic Pathology, Department of Pathology, Beaumont Health System, Royal Oak, MI, USA Ping.Zhang@Beaumont.edu.
Objective:
Vascular endothelial growth factor (VEGF) antagonists have been used for treating metastatic neoplasms. It has also been known that one of its side effects is to cause proteinuria and renal failure in the setting of thrombotic microangiopathy (TMA). The underlying mechanism is likely due to the inhibition of VEGF production in podocytes, resulting in diffuse fusion of foot processes and impaired glomerular endothelial fenestrations, and leading to massive proteinuria and subsequent glomerular endothelium injury. Intravitreal injection of VEGF antagonists (IIVA) has been also used to treat macular degeneration and diabetic retinal neo-vascular proliferation. The majority of patients tolerate the treatment well. However, IIVA can lead to renal dysfunction including proteinuria and gradual renal failure as a rare side effect. The goal of this study was to report two cases related to the nephrotoxicity of IIVA and review the literature associated with this topic.
Case Report:
The first diabetic patient had elevated serum creatinine at 3.25 mg/dl and proteinuria/creatinine ratio at 6.1 after 48-month treatment of IIVA. The first renal biopsy revealed thrombotic microangiopathy that was correlated with his increased serum creatinine and nephrotic range of proteinuria. The second diabetic patient had increased serum creatinine up to 1.89 mg/dl but low proteinuria. The second biopsy showed acute tubular necrosis that was correlated with his elevated serum creatinine.
Conclusion:
Intravitreal injection of VEGF antagonist can be associated with thrombotic microangiopathy and acute tubular necrosis, leading to renal dysfunction.
Insights
Intravitreal injections of vascular endothelial growth factor (VEGF) antagonists can rarely cause kidney damage, including thrombotic microangiopathy and acute tubular necrosis. This highlights potential renal risks associated with anti-VEGF eye treatments.
Area of Science:
- Ophthalmology
- Nephrology
- Oncology
Background:
- Vascular endothelial growth factor (VEGF) antagonists are utilized in treating metastatic cancers and neovascular eye conditions.
- A known side effect of systemic VEGF antagonists is proteinuria and renal failure, particularly thrombotic microangiopathy (TMA).
- Intravitreal injection of VEGF antagonists (IIVA) is a common treatment for retinal diseases, generally well-tolerated.
Observation:
- This study reports two cases of diabetic patients experiencing renal dysfunction after IIVA.
- Case 1: A patient developed thrombotic microangiopathy with elevated creatinine and nephrotic proteinuria after 48 months of IIVA.
- Case 2: Another patient presented with acute tubular necrosis and elevated creatinine, despite low proteinuria.
Findings:
- Renal biopsies confirmed thrombotic microangiopathy in the first patient and acute tubular necrosis in the second.
- These findings correlate with the observed renal dysfunction and elevated serum creatinine levels.
- The mechanism may involve impaired VEGF function in podocytes, leading to glomerular injury.
Implications:
- Intravitreal VEGF antagonists, despite localized administration, can induce systemic nephrotoxicity.
- Clinicians should monitor renal function in patients receiving IIVA, especially those with pre-existing kidney conditions.
- Further research is needed to elucidate the precise mechanisms and risk factors for IIVA-induced nephrotoxicity.
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