Key result
Higher urinary retinol-binding protein is linked to lower eGFR in stage 3 and 4 CKD.
Why the study?
Whether urinary retinol-binding protein is a biomarker of renal damage and CKD progression in general chronic kidney disease was not known.
Is urinary retinol-binding protein associated with renal function and cardiovascular risk factors in patients with stages 3 and 4 CKD?
Cross-Sectional (n=454)
No
Is urinary retinol-binding protein associated with renal function and cardiovascular risk factors in patients with stages 3 and 4 CKD?
Effect estimate: β -0.02 (95% CI -0.02; -0.01)
p-value: p=<0.0001
Urinary RBP is inversely associated with eGFR in stages 3 and 4 CKD and improves the diagnostic accuracy for reduced renal function, suggesting its potential as a biomarker beyond specific tubulopathies.
Urinary RBP links independently to lower eGFR in general CKD; leaves open its value for progression prediction pending longitudinal data.
The role of urinary retinol-binding protein (RBP) as a biomarker of CKD in proximal tubular diseases, glomerulopathies and in transplantation is well established. However, whether urinary RBP is also a biomarker of renal damage and CKD progression in general CKD is not known. In this study, we evaluated the association of urinary RBP with renal function and cardiovascular risk factors in the baseline data of the Progredir Study, a CKD cohort in Sao Paulo, Brazil, comprising 454 participants with stages 3 and 4 CKD. In univariate analysis, urinary RBP was inversely related to estimated glomerular filtration rate (CKD-EPI eGFR) and several cardiovascular risk factors. After adjustments, however, only CKD-EPI eGFR, albuminuria, systolic blood pressure, anemia, acidosis, and left atrium diameter remained significantly related to urinary RBP. The inverse relationship of eGFR to urinary RBP (β-0.02 ± 95CI -0.02; -0.01, p<0.0001 for adjusted model) remained in all strata of albuminuria, even after adjustments: in normoalbuminuria (β-0.008 ± 95CI (-0.02; -0.001, p = 0.03), in microalbuminuria (β-0.02 ± 95CI (-0.03; -0.02, p<0,0001) and in macroalbuminuria (β-0.02 ± 95CI (-0.03; -0.01, p<0,0001). Lastly, urinary RBP was able to significantly increase the accuracy of a logistic regression model (adjusted for sex, age, SBP, diabetes and albuminuria) in diagnosing eGFR<35 ml/min/1.73m2 (AUC 0,77, 95%CI 0,72-0,81 versus AUC 0,71, 95%CI 0,65-0,75, respectively; p = 0,05). Our results suggest that urinary RBP is significantly associated to renal function in CKD in general, a finding that expands the interest in this biomarker beyond the context of proximal tubulopathies, glomerulopathies or transplantation. Urinary RBP should be further explored as a predictive marker of CKD progression.
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Domingos et al. (2016) conducted a cross-sectional in Stages 3 and 4 Chronic Kidney Disease (CKD) (n=454). Urinary retinol-binding protein (RBP) was evaluated on Estimated glomerular filtration rate (CKD-EPI eGFR) (β -0.02, 95% CI -0.02; -0.01, p=<0.0001). Urinary retinol-binding protein was significantly and inversely associated with estimated glomerular filtration rate (β -0.02) in patients with stages 3 and 4 chronic kidney disease.
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