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Soluble Urokinase-Type Plasminogen Activator Receptor in Black Americans with CKD. | LitMetric

Background And Objectives: Black Americans with and without kidney disease risk variants face high risk of ESKD. Soluble urokinase-type plasminogen activator receptor (suPAR), a circulating signaling protein and marker of immune activation, constitutes a promising biomarker of CKD-associated risks. We aimed to quantify the associations between serum suPAR concentration and adverse outcomes in Black Americans with and without kidney disease risk variants, over and above iodine-125 iothalamate measured GFR and proteinuria.

Design, Setting, Participants, & Measurements: Using data from the African-American Study of Kidney Disease and Hypertension, a multicenter clinical trial followed by a cohort phase with a median total follow-up of 9.7 years (interquartile range, 6.5-10.9 years), we examined the associations of suPAR with CKD progression (defined as doubling of serum creatinine or ESKD), ESKD, worsening proteinuria (defined as pre-ESKD doubling of 24-hour urine protein-to-creatinine ratio to ≥220 mg/g), and all-cause death.

Results: At baseline, the median suPAR was 4462 pg/ml, mean measured GFR was 46 ml/min per 1.73 m, and median 24-hour urine protein-to-creatinine ratio was 80 mg/g. After controlling for baseline demographics, randomization arm, GFR, proteinuria, risk status, and clinical risk factors, there was a 1.26-times higher risk for CKD progression per SD higher baseline log-transformed suPAR (hazard ratio [HR], 1.26; 95% confidence interval [95% CI], 1.11 to 1.43; <0.001). Higher suPAR was also independently associated with risk of ESKD (HR, 1.36; 95% CI, 1.17 to 1.58; <0.001) and death (HR, 1.25; 95% CI, 1.08 to 1.45; =0.003). suPAR was only associated with worsening proteinuria in patients with two risk alleles (HR, 1.46; 95% CI, 1.08 to 1.99; =0.02).

Conclusions: Higher suPAR was associated with various adverse outcomes in Black Americans with CKD, with and without kidney disease risk variants, independently of proteinuria and GFR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6032570PMC
http://dx.doi.org/10.2215/CJN.13631217DOI Listing

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