TY - JOUR
T1 - Diagnostic performance of 2D-shear wave elastography and serum fibrosis markers for evaluation of hepatic graft fibrosis in pediatric liver-inclusive transplant recipients
T2 - A prospective pilot study
AU - Vo, Hanh D.
AU - Radio, Stanley J.
AU - Granader, Elon J.
AU - Wojkiewicz, Laura E.
AU - Turner, Patricia
AU - Mauch, Teri J.
N1 - Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022/6
Y1 - 2022/6
N2 - Background: Liver biopsy is the gold standard for hepatic fibrosis staging, but it is invasive and has potential severe complications. We aimed to determine the diagnostic performance of 2D-SWE and serum markers to predict significant hepatic graft fibrosis (≥F2) in pediatric liver-inclusive transplant recipients. Methods: This prospective, cross-sectional pilot study included children younger than 19 years who had received a LT or LSBT and underwent a liver biopsy performed for clinical indications. LS was measured using 2D-SWE. The AUROC was calculated to evaluate the diagnostic performance of 2D-SWE and biomarkers (AST/ALT ratio, APRI, FIB4) for predicting significant fibrosis. Results: Twenty-two children (13 males, 8 LSBT) were included. Eighteen (81.8%) children received a whole liver graft. Thirteen (59.1%) patients had hepatic fibrosis (≥F1) and four (18.2%) had significant fibrosis. The AUROCs of AST/ALT ratio, APRI, and FIB4 for predicting significant hepatic graft fibrosis were 0.71 (p =.29), 0.85 (p =.0001), and 0.76 (p =.03), respectively. When FIB4 was calculated using the hepatic graft's age, its AUROC improved to 0.85 (p <.0001). The AUROC of 2D-SWE for predicting significant hepatic graft fibrosis was 0.80 (p =.046). When 2D-SWE was combined with APRI or FIB4, its AUROC improved to 0.82 (p =.08) and 0.87 (p =.002), respectively. Conclusions: APRI and FIB4 can accurately predict significant hepatic graft fibrosis. 2D-SWE may serve as a valuable adjunct tool to detect significant graft fibrosis, especially when combined with these serum markers.
AB - Background: Liver biopsy is the gold standard for hepatic fibrosis staging, but it is invasive and has potential severe complications. We aimed to determine the diagnostic performance of 2D-SWE and serum markers to predict significant hepatic graft fibrosis (≥F2) in pediatric liver-inclusive transplant recipients. Methods: This prospective, cross-sectional pilot study included children younger than 19 years who had received a LT or LSBT and underwent a liver biopsy performed for clinical indications. LS was measured using 2D-SWE. The AUROC was calculated to evaluate the diagnostic performance of 2D-SWE and biomarkers (AST/ALT ratio, APRI, FIB4) for predicting significant fibrosis. Results: Twenty-two children (13 males, 8 LSBT) were included. Eighteen (81.8%) children received a whole liver graft. Thirteen (59.1%) patients had hepatic fibrosis (≥F1) and four (18.2%) had significant fibrosis. The AUROCs of AST/ALT ratio, APRI, and FIB4 for predicting significant hepatic graft fibrosis were 0.71 (p =.29), 0.85 (p =.0001), and 0.76 (p =.03), respectively. When FIB4 was calculated using the hepatic graft's age, its AUROC improved to 0.85 (p <.0001). The AUROC of 2D-SWE for predicting significant hepatic graft fibrosis was 0.80 (p =.046). When 2D-SWE was combined with APRI or FIB4, its AUROC improved to 0.82 (p =.08) and 0.87 (p =.002), respectively. Conclusions: APRI and FIB4 can accurately predict significant hepatic graft fibrosis. 2D-SWE may serve as a valuable adjunct tool to detect significant graft fibrosis, especially when combined with these serum markers.
KW - 2D-shear wave elastography
KW - children
KW - fibrosis markers
KW - liver elasticity
KW - liver graft fibrosis
KW - liver transplant
UR - http://www.scopus.com/inward/record.url?scp=85122687666&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85122687666&partnerID=8YFLogxK
U2 - 10.1111/petr.14225
DO - 10.1111/petr.14225
M3 - Article
C2 - 35005824
AN - SCOPUS:85122687666
SN - 1397-3142
VL - 26
JO - Pediatric Transplantation
JF - Pediatric Transplantation
IS - 4
M1 - e14225
ER -