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.

Abstract

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.