AI Article Synopsis

  • This study examined the prognostic value of urinary liver-type fatty-acid-binding protein (L-FABP) levels in predicting long-term adverse outcomes for patients in cardiac intensive care units, along with serum creatinine-defined acute kidney injury (AKI).
  • Out of 1119 patients (average age 68), nearly half had acute coronary syndrome, and about one-third had acute decompensated heart failure; key findings indicated that elevated L-FABP levels and creatinine-defined AKI both significantly correlated with increased risk of death or progression to end-stage kidney disease over an average follow-up of 41 months.
  • The study concluded that measuring L-FABP on admission could enhance long-term risk assessment

Article Abstract

We prospectively investigated the prognostic value of urinary liver-type fatty-acid-binding protein (L-FABP) levels on hospital admission, both independently and in combination with serum creatinine-defined acute kidney injury (AKI), to predict long-term adverse outcomes in 1119 heterogeneous patients (mean age; 68 years) treated at medical (non-surgical) cardiac intensive care units (CICUs). Patients with stage 5 chronic kidney disease were excluded from the study. Of these patients, 47% had acute coronary syndrome and 38% had acute decompensated heart failure. The creatinine-defined AKI was diagnosed according to the "Kidney Disease: Improving Global Outcomes" criteria. The primary endpoint was a composite of all-cause death or progression to end-stage kidney disease, indicating the initiation of maintenance dialysis therapy or kidney transplantation. Creatinine-defined AKI occurred in 207 patients, with 44 patients having stage 2 or 3 disease. During a mean follow-up period of 41 months after enrollment, the primary endpoint occurred in 242 patients. Multivariate Cox regression analyses revealed L-FABP levels as independent predictors of the primary endpoint ( < 0.001). Adding L-FABP to a baseline model with established risk factors further enhanced reclassification and discrimination beyond that of the baseline model alone, for primary-endpoint prediction (both; < 0.01). On Kaplan-Meier analyses, increased L-FABP (≥4th quintile value of 9.0 ng/mL) on admission or presence of creatinine-defined AKI, correlated with an increased risk of the primary endpoint ( < 0.001). Thus, urinary L-FABP levels on admission are potent and independent predictors of long-term adverse outcomes, and they might improve the long-term risk stratification of patients admitted at medical CICUs, when used in combination with creatinine-defined AKI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073895PMC
http://dx.doi.org/10.3390/jcm9020482DOI Listing

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