Predicting Progression of Chronic Kidney Disease in Sickle Cell Anemia Using Machine Learning Models (PREMIER)

点击翻译按钮获取中文摘要

ABSTRACT Sickle cell disease (SCD) is characterized by a vasculopathy affecting multiple end organs, with complications including chronic kidney disease (CKD). Albuminuria, an early measure of glomerular injury, is common in SCD and predicts progressive kidney disease. Kidney function decline is faster in SCD patients than in the general African American population. The prevalence of rapid decline in SCD is 3-fold higher than in the general population. Furthermore, high-risk APOL1 variants are associated with an increased risk of albuminuria and progression of CKD in SCD. Kidney disease, regardless of severity, and rapid eGFR decline are associated with increased mortality in SCD. As such, early identification of patients at risk for progression of CKD is important to address potentially modifiable risk factors, slow eGFR decline and reduce mortality. Despite the high prevalence of CKD and its contribution to increased morbidity and mortality, available treatments for SCD-related kidney disease remain limited. Although angiotensin converting enzyme inhibitors (ACE-I), angiotensin receptor blockers (ARBs), and hydroxyurea decrease albuminuria in short-term studies, their benefits in preventing or slowing progressive loss of kidney function in SCD remain undefined. We have recently reported that machine learning (ML) models can identify patients at high risk for rapid decline in kidney function. Further, higher hemoglobin concentration is also an independent predictor of decreased odds of rapid kidney function decline. With the contribution of intravascular hemolysis to the pathophysiology of SCD-related glomerulopathy, voxelotor, a small molecule which modifies sickle hemoglobin oxygen affinity and improves sickle RBC survival, may decrease glomerular injury and slow the progression of CKD in individuals with SCD. In this application, we propose the conduct of a prospective, multicenter study to build a ML-based predictive model for progression of CKD in adults with SCD. Furthermore, in individuals predicted to be at risk for rapid decline in kidney function, based on the presence of persistent albuminuria (urine ACR ≥ 100 mg/g), we will evaluate the effect of voxelotor on albuminuria, rapid decline in kidney function and progression of CKD. With advances in the understanding of the pathophysiology of SCD and its complications, combined with an increasing number of approved drug therapies, early identification of patients at risk for progressive kidney disease and subsequent increased risk of death is necessary to modify known risk factors, initiate targeted therapies and possibly increase life expectancy. Further, with the known contribution of hemolytic anemia to the pathogenesis of SCD-related glomerulopathy and progressive kidney disease, drugs that decrease hemolysis are likely to be beneficial in preventing and/or slowing the progression of kidney disease in this patient population.