Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 24, Issue 3, Pages -Publisher
MDPI
DOI: 10.3390/ijms24031826
Keywords
acute kidney injury; pre-renal; intrinsic; injury biomarkers; anamnesis; etiopathology
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Acute kidney injury (AKI) is a sudden renal dysfunction syndrome with severe consequences, and its etiology plays a role in the prognosis. Differentiating between pre-renal and intrinsic AKI is challenging using international diagnostic criteria, so additional biochemical criteria and patient history are necessary. A composite biochemical criterion, based on the congruency of at least two ratios, is proposed to minimize confounding factors. Urinary injury biomarkers, such as NGAL and KIM-1, better coincide with the biochemical classification and support an etiological diagnosis based on objective parameters.
Acute kidney injury (AKI) is a syndrome of sudden renal excretory dysfunction with severe health consequences. AKI etiology influences prognosis, with pre-renal showing a more favorable evolution than intrinsic AKI. Because the international diagnostic criteria (i.e., based on plasma creatinine) provide no etiological distinction, anamnestic and additional biochemical criteria complement AKI diagnosis. Traditional, etiology-defining biochemical parameters, including the fractional excretion of sodium, the urinary-to-plasma creatinine ratio and the renal failure index are individually limited by confounding factors such as diuretics. To minimize distortion, we generated a composite biochemical criterion based on the congruency of at least two of the three biochemical ratios. Patients showing at least two ratios indicative of intrinsic AKI were classified within this category, and those with at least two pre-renal ratios were considered as pre-renal AKI patients. In this study, we demonstrate that the identification of intrinsic AKI by a collection of urinary injury biomarkers reflective of tubular damage, including NGAL and KIM-1, more closely and robustly coincide with the biochemical than with the anamnestic classification. Because there is no gold standard method for the etiological classification of AKI, the mutual reinforcement provided by the biochemical criterion and urinary biomarkers supports an etiological diagnosis based on objective diagnostic parameters.
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