Abstract

The objective of this study was to investigate renal function in a cohort of 98 patients with sickle cell disease (SCD) followed up at a tertiary hospital in Brazil. Clinical and laboratory characteristics at the time of the most recent medical examination were analyzed. Renal function was evaluated by the estimation of glomerular filtration rate (GFR) by the criteria of the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI). We compared patients with normal GFR to patients with decreased GFR (<60 mL·min−1·(1.73 m2)−1) and hyperfiltration (>120 mL·min−1·(1.73 m2)−1). Comparison between patients according to the use of hydroxyurea and comparison of clinical and laboratory parameters according to GFR were also carried out. Average patient age was 33.8 ± 13.3 years (range 19-67 years), and 57 (58.1%) patients were females. The comparison of patients according to GFR showed that patients with decreased GFR (<60 mL·min−1·(1.73 m2)−1) were older, had lower levels of hematocrit, hemoglobin and platelets and higher levels of urea and creatinine. Independent risk factors for decreased GFR were advanced age (OR = 21.6, P < 0.0001) and anemia (OR = 39.6, P < 0.0001). Patients with glomerular hyperfiltration tended to be younger, had higher levels of hematocrit, hemoglobin and platelets and lower levels of urea and creatinine, with less frequent urinary abnormalities. Hydroxyurea, at the dosage of 500-1000 mg/day, was being administered to 28.5% of the patients, and there was no significant difference regarding renal function between the two groups. Further studies are required to establish the best therapeutic approach to renal abnormalities in SCD.

Highlights

  • Sickle cell disease (SCD) is the most common hereditary hematologic disease in the world and is a Public Health problem in tropical countries [1]

  • The present study investigated the occurrence of renal Previous studies found higher glomerular filtration rate (GFR) and increased renal www.bjournal.com.br plasma flow in patients with SCD compared Table 3

  • Comparison of patients with sickle cell disease according to the use of to controls [5]

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Summary

Introduction

Sickle cell disease (SCD) is the most common hereditary hematologic disease in the world and is a Public Health problem in tropical countries [1]. In Brazil, the prevalence of SCD among Afro-descendants is 0.1-0.3% [2]. Renal abnormalities in SCD include microalbuminuria, proteinuria, tubular dysfunction, and glomerulopathies [1,3]. Patients with SCD have abnormalities in renal hemodynamics, and young patients present increased glomerular filtration rate (GFR), which seems to be associated with increased sensitivity to prostaglandins, since treatment with indomethacin significantly reduces GFR among these patients [1]. The objective of this study was to investigate renal function abnormalities in SCD patients in Brazil

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