Endotrophin as a Biomarker for Severe Acute Kidney Injury and Major Adverse Kidney Events

Background The search for novel biomarkers in AKI continues, both for being able to predict adverse events in AKI but also for confirming pathogenic pathways as potential therapeutic targets. Endotrophin (ETP) is an emerging biomarker in a number of fibroinflammatory diseases. We sought to test the association of ETP with the development of a major adverse kidney event (MAKE) in critically ill adult patients. Methods Single-center prospective study of critically ill adult patients with stage 2-3 AKI and patients without AKI. Serum ETP was measured early in the first 3 days of critical care admission, 5-7 days later, and in some patients, 4-6 weeks later. The primary outcome was MAKE assessed at hospital discharge, a composite of mortality, RRT at discharge, and eGFR reduction of >= 25% from baseline. Results Among 121 patients evaluated in this study, serum ETP was significantly higher in patients with AKI versus those without (P < 0.05). In multivariable logistic regression analysis, higher tertiles of ETP were significantly associated with MAKE at discharge, controlled for relevant covariates. Furthermore, sustained elevations in ETP 5-7 days later, as opposed to reductions toward normal, were also associated with MAKE. In patients seen in the clinic 4-6 weeks post-AKI, ETP remained elevated. In the acute period, ETP levels correlated most with TNF-alpha and neutrophil gelatinase-associated lipocalin. Conclusions Higher levels of serum ETP early in the intensive care unit admission, as well as sustained elevations of ETP within a 5-day to 7-day period, are associated with MAKE at hospital discharge. ETP is a potential biomarker of AKI-related outcomes and a promising therapeutic target to minimize sequelae of AKI.