Although it is recognized that sickle cell disease (SCD) is characterized by the presence of endothelial dysfunction, the contribution of endothelial dysfunction to disease pathophysiology remains poorly defined. We, and others, have previously reported on an association of pulmonary hypertension and nephropathy in patients with SCD, suggesting that they may share a similar pathophysiology. More recently, we have found that SCD patients with macroalbuminuria (urine albumin excretion >300 mg/g creatinine) have significantly elevated levels of both soluble vascular cell adhesion molecule-1 (VCAM-1), a measure of endothelial activation, and soluble fms-like tyrosine kinase-1 (sFLT-1), a member of the VEGF receptor family. sFLT-1 is known to induce endothelial dysfunction by sequestration of VEGF in plasma and/or by the formation of inactive receptors and reduced signal transduction. In addition, we found that sFLT-1 was significantly correlated with soluble VCAM-1 in SCD patients. This data, combined with the association of sFLT-1 with proteinuria in other disease states (such as preeclampsia) suggests that by inducing endothelial dysfunction, sFLT-1 may play an important role in the development of albuminuria in SCD. In the current application, we will define the contribution of endothelial dysfunction as well as the sFLT-1/VEGF axis to the pathogenesis of albuminuria in SCD patients and transgenic sickle cell mice. Furthermore, we will evaluate the effect of atorvastatin, an agent that is known to attenuate endothelial dysfunction and decrease sFLT-1 release, on endothelial dysfunction and albuminuria. With the limited therapies available for the treatment of SCD-related nephropathy, the demonstration of a role for endothelial dysfunction in the pathogenesis of albuminuria will facilitate the development of more effective treatments.
The contribution of endothelial dysfunction to the pathophysiology of sickle cell disease (SCD) remains poorly defined. However, patients with certain SCD-related complications such as albuminuria and pulmonary hypertension are known to exhibit evidence of endothelial dysfunction based on increased levels of soluble vascular cell adhesion molecule-1 (VCAM-1). Furthermore, these patients manifest evidence of increased levels of soluble fms-like tyrosine kinase-1 (sFLT-1), a member of the VEGF receptor family that is known to induce endothelial dysfunction. In this application, we will explore the contribution of endothelial dysfunction, as well as the sFLT-1/VEGF axis to the pathogenesis of albuminuria in SCD by addressing the following specific aims: We will evaluate the association of albuminuria with endothelial dysfunction, assessed non-invasively by ultrasound imaging of the brachial artery, in patients with sickle cell disease;we will test the hypothesis that in transgenic sickle cell mice, altered regulation of VEGF by sFLT-1 results in glomerular endothelial dysfunction and albuminuria;and finally, we will evaluate the effect of atorvastatin on endothelial dysfunction and albuminuria in patients with sickle cell disease.
|Ataga, Kenneth I; Stocker, Jonathan (2015) The trials and hopes for drug development in sickle cell disease. Br J Haematol 170:768-80|
|Freeman, Ashley T; Ataga, Kenneth I (2015) Pulmonary endarterectomy as treatment for chronic thromboembolic pulmonary hypertension in sickle cell disease. Am J Hematol 90:E223-4|
|Ataga, Kenneth I; Hinderliter, Alan; Brittain, Julia E et al. (2015) Association of pro-inflammatory high-density lipoprotein cholesterol with clinical and laboratory variables in sickle cell disease. Hematology 20:289-96|
|Wongtong, Naritsara; Jones, Susan; Deng, Yu et al. (2015) Monocytosis is associated with hemolysis in sickle cell disease. Hematology 20:593-7|
|Desai, Payal C; Deal, Allison M; Pfaff, Emily R et al. (2015) Alloimmunization is associated with older age of transfused red blood cells in sickle cell disease. Am J Hematol 90:691-5|
|Buckner, Tyler W; Ataga, Kenneth I (2014) Does hydroxyurea prevent pulmonary complications of sickle cell disease? Hematology Am Soc Hematol Educ Program 2014:432-7|
|Ataga, Kenneth I; Klings, Elizabeth S (2014) Pulmonary hypertension in sickle cell disease: diagnosis and management. Hematology Am Soc Hematol Educ Program 2014:425-31|
|Ataga, Kenneth I; Derebail, Vimal K; Archer, David R (2014) The glomerulopathy of sickle cell disease. Am J Hematol 89:907-14|
|Laurin, Louis-Philippe; Nachman, Patrick H; Desai, Payal C et al. (2014) Hydroxyurea is associated with lower prevalence of albuminuria in adults with sickle cell disease. Nephrol Dial Transplant 29:1211-8|
|Desai, Payal C; Ataga, Kenneth I (2013) The acute chest syndrome of sickle cell disease. Expert Opin Pharmacother 14:991-9|
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