Abstract

Background: Proliferative diabetic retinopathy (PDR) is one of the most important microvascular complications among the patients with diabetes. Intravitreal anti-vascular endothelial growth factor (anti-VEGF) agent enacts a key role in PDR. Some studies have dealt with the systemic exposure to these agents after intravitreal administration. However, renal dysfunction following this therapy has scarcely been reported. Hence, this study aimed to determine the effect of intravitreal bevacizumab treatment on the deterioration of renal function and proteinuria.Materials and Methods: This present prospective observational study was performed on 40 patients with diabetic nephropathy and PDR and/or significant diabetic macular edema as the candidates for receiving intravitreal injection of bevacizumab. To evaluate renal function, changes in the urinary albumin-to-creatinine ratio (UACR), serum creatinine (SCr), and estimated glomerular filtration rate (eGFR) one month after injection were measured. Also, changes in systolic and diastolic blood pressures (BPs), plasma VEGF level, platelet, white blood cell (WBC) counts, and hemoglobin (Hb) level were measured at the baseline and one month after treatment.Results: The mean age of the patients was 60.3 ± 9.2 years, and 33 patients were female. The decrease in the plasma VEGF level and platelet count, as well as the increase in diastolic BP, and Hb level were significant. However, systolic BP and WBC count remained unchanged. There were no significant changes in UACR, SCr, and eGFR after the injection as compared to baseline (P>0.05).Conclusion: Our study indicated that intravitreal bevacizumab injection was not associated with renal dysfunction and proteinuria in patients with diabetic nephropathy. Nevertheless, diastolic BP and Hb level could increase after one month. [GMJ.2018;In press:e1299]

Highlights

  • In recent years, some evidence has indicated the important role of vascular endothelial growth factor (VEGF) in the development of proliferative diabetic retinopathy (PDR) and diabetic macular edema (DME) [1]

  • The intravitreal injection of bevacizumab is not approved by the Food and Drug Administration (FDA), it is widely used for the off-label treatment of PDR and DME

  • There was no significant correlation between the decrease in plasma VEGF levels and changes in urinary albumin-to-creatinine ratio (UACR) (r = -0.01, P = 0.94)

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Summary

Introduction

Some evidence has indicated the important role of vascular endothelial growth factor (VEGF) in the development of proliferative diabetic retinopathy (PDR) and diabetic macular edema (DME) [1]. The intravenous administration of bevacizumab is used as an adjuvant therapy for many advanced cancers and has been associated with a significant reduction in the plasma VEGF level causing important adverse effects including hypertension, proteinuria, renal dysfunction, and thromboembolism [3, 4]. Changes in systolic and diastolic blood pressures (BPs), plasma VEGF level, platelet, white blood cell (WBC) counts, and hemoglobin (Hb) level were measured at the baseline and one month after treatment. Conclusion: Our study indicated that intravitreal bevacizumab injection was not associated with renal dysfunction and proteinuria in patients with diabetic nephropathy. Diastolic BP and Hb level could increase after one month.[GMJ.2018;7:e1299] DOI:10.22086/gmj.v0i0.1299

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