Abstract

Background & AimsChronic liver disease (CLD) represents a major risk for mortality and, while challenging, early detection is key to improve overall outcome. Triggering receptor expressed on myeloid cells 2 (TREM2)-expressing macrophages and systemic levels of soluble TREM2 (sTREM2) appear critical in the development of CLD and seem relevant in its detection. The aim of this study was to examine sTREM2 as a marker for early CLD and its potential to predict posthepatectomy liver failure (PHLF) in patients undergoing partial hepatectomy. MethodsSTREM2 was assessed in plasma of 108 patients undergoing liver resection. Blood was drawn prior to surgery (preop) and on the first and fifth postoperative day. ResultsPreop sTREM2 levels were similar across different indications for resection (p=0.091). Higher preop sTREM2 levels were associated with advanced hepatic fibrosis (p=0.030) and PHLF (p=0.007). Fibrosis-4 index (FIB-4) (p=0.619) and Model for End Stage Liver Disease (MELD) (p=0.590) did not show a difference between patients grouped by their CLD. Comparing the area under the curve from receiver operating characteristic analysis, sTREM2 (AUC=0.708) outperformed FIB-4 (AUC=0.529), MELD (AUC=0.587), Child-Pugh grading (AUC=0.570) and liver maximum capacity test (LiMAx) (AUC=0.516) in predicting PHLF. Similarly, in uni- and multivariate analysis only sTREM2 proved predictive for PHLF (p=0.023). A high- (p=0.003) and low-risk cutoff (p=0.011) for systemic sTREM2 levels were able to identify patients at risk for adverse outcome after surgery. Finally, high sTREM2 was associated with decreased overall survival after liver surgery (p<0.001). ConclusionsCirculating sTREM2 shows sensitivity for early-stage, asymptomatic liver disease, irrespective of the underlying indication for liver surgery. Assessment of CLD via sTREM2 monitoring could improve early detection of CLD and improve outcome after liver surgery. Impact and ImplicationsSoluble TREM2 (sTREM2) has previously been established to correlate with the degree of chronic liver disease. We found that even in patients undergoing liver resection, who generally do not suffer from end stage liver disease, sTREM2 reflects liver fibrosis status and predicts postoperative development of liver dysfunction. This is especially relevant for liver surgeons and patients, as postoperative liver dysfunction is the main reason for postoperative mortality. Our findings are also important for hepatologists, as early detection of liver fiboris and cirrhosis is paramount for overall patient survival and we can show that even in a cohort with a median MELD of 6, sTREM2 is able to distuinguish patients based on their liver fibrosis status.

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