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      Renal functional reserve and renal recovery after acute kidney injury.

      Nephron. Clinical practice
      Acute Kidney Injury, complications, physiopathology, therapy, Age Factors, Cardio-Renal Syndrome, Cardiovascular System, Comorbidity, Creatinine, blood, Dietary Proteins, diagnostic use, Female, Glomerular Filtration Barrier, Glomerular Filtration Rate, Humans, Kidney, Kidney Function Tests, methods, Living Donors, Male, Pregnancy, Pregnancy Complications, Recovery of Function, Renal Insufficiency, Chronic, etiology, Stress, Physiological, Tissue and Organ Procurement, standards

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          Abstract

          Renal functional reserve (RFR) represents the capacity of the kidney to increase glomerular filtration rate (GFR) in response to certain physiological or pathological stimuli or conditions. Once baseline GFR is determined, RFR can be assessed clinically after an oral protein load or intravenous amino acid infusion. In clinical practice, baseline GFR displays variable levels due to diet or other factors. RFR is the difference between peak 'stress' GFR induced by the test (p.o. or i.v.) and the baseline GFR. In clinical scenarios where hyperfiltration is present (high baseline GFR due to pregnancy, hypertension or diabetic nephropathy, in solitary kidney or kidney donors), RFR may be fully or partially used to achieve normal or supranormal renal function. Since commonly used renal function markers, such as GFR, may remain within normal ranges until 50% of nephrons are lost or in patients with a single remnant kidney, the RFR test may represent a sensitive and early way to assess the functional decline in the kidney. RFR assessment may become an important tool to evaluate the ability of the kidney to recover completely or partially after a kidney attack. In case of healing with a defect and progressive fibrosis, recovery may appear complete clinically, but a reduced RFR may be a sign of a maladaptive repair or subclinical loss of renal mass. Thus, a reduction in RFR may represent the equivalent of renal frailty or susceptibility to insults. The main aim of this article is to review the concept of RFR, its utility in different clinical scenarios, and future perspective for its use. 2014 S. Karger AG, Basel.

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          Most cited references15

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          Age changes in glomerular filtration rate, effective renal plasma flow, and tubular excretory capacity in adult males.

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            Predicting progression to chronic kidney disease after recovery from acute kidney injury.

            This review examines the association between acute kidney injury (AKI) and subsequent risk for chronic kidney disease (CKD) development. The discussion focuses on patients who fully recover from an episode of AKI, the majority of whom do not receive follow-up care with nephrology services. Several studies have demonstrated a strong association between AKI and later CKD risk. Animal models provide evidence for a causal link between AKI and CKD while also elucidating some of the potential mechanisms for this progression. Large observational studies have quantified the risk of CKD following AKI recovery, and clinical and emerging biomarker risk factors have been identified. The association between AKI with incomplete recovery or nonrecovery and CKD is evident. Recent studies demonstrate that even AKI with apparent full recovery confers an increased risk for subsequent CKD development. Risk prediction models have been developed and require further refinement and validation. The ability to identify patients with AKI recovery who are at high risk for later CKD development is an important clinical and research goal, as there exists a significant opportunity to improve care in this population.
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              Renal functional reserve in humans

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