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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Effect of renin-angiotensin-aldosterone system blocking agents on progression of glomerulopathy in sickle cell
Ashley Thrower1, Emily J Ciccone2, Poulami Maitra3
1School of Medicine, University of North Carolina, Chapel Hill, NC, USA.
Insights
Renin-angiotensin-aldosterone system (RAAS) blocking agents did not significantly differ in reducing proteinuria long-term for sickle cell disease (SCD) patients. However, RAAS blockade may slow the decline in kidney function (eGFR) in these patients.
Area of Science:
- Nephrology
- Hematology
- Pharmacology
Background:
- Renin-angiotensin-aldosterone system (RAAS) inhibitors are known to reduce albuminuria short-term.
- Long-term efficacy of RAAS blockers in sickle cell disease (SCD) remains unconfirmed.
- Kidney disease is a significant complication in SCD.
Purpose of the Study:
- To evaluate the long-term effects of RAAS blocking agents on proteinuria and estimated glomerular filtration rate (eGFR) decline in patients with SCD.
- To compare the outcomes of SCD patients on RAAS blockers versus those not on treatment.
Main Methods:
- Retrospective, single-center study.
- Compared 86 SCD patients on RAAS blockers for proteinuria with 68 SCD patients not on RAAS blockers.
- Median follow-up of approximately 2.3 years.
Main Results:
- Proteinuria decreased over time in both groups, with no statistically significant difference between them.
- Estimated glomerular filtration rate (eGFR) declined in both groups, but the decline was significantly slower in patients on RAAS blocking agents.
- RAAS blocking agents did not significantly affect mortality, though baseline eGFR was associated with mortality.
Conclusions:
- RAAS blockade may slow the rate of kidney function loss in patients with SCD.
- Further research is needed to confirm the long-term benefits of RAAS inhibitors in SCD nephropathy.
Abstract:
Although renin-angiotensin-aldosterone system (RAAS) blocking agents decrease albuminuria in short-term studies, there is no evidence confirming their long-term efficacy in sickle cell disease (SCD). In a single-centre, retrospective study, we evaluated the long-term effect of RAAS blocking agents on proteinuria and declining estimated glomerular filtration rates (eGFR). Eighty-six patients on RAAS blocking agents for proteinuria, followed for a median of 2·28 years, were compared with 68 patients with proteinuria followed for 2·24 years who were not receiving such treatment. The log odds of proteinuria decreased over time in patients on RAAS blocking agents (β: -0·23, P = 0·03) and in the non-treatment group (β: -0·54, P < 0·0001), but was not statistically different between both groups (β: 0·31, P = 0·063). The eGFR declined over time in patients on RAAS blocking agents (β: -2·78, P < 0·0001) and in those not on such treatment (β: -4·7, P < 0·0001), and was statistically different between both groups (β: 1·9, P = 0·0002). Baseline eGFR was associated with mortality (Hazard rato: 0·97, P < 0·0001), but RAAS blocking agents had no significant effect on mortality. These data suggest that RAAS blockade may slow the loss of kidney function in SCD.
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