Abstract 4372594: Cholate clearance as assessed by HepQuant-SHUNT is predictive of clinical outcomes in individuals with Fontan circulation

Y Yuli Kim (Hospital of the University of Penn, Philadelphia, Pennsylvania, United States) D Daniel Ganger (Northwestern University, Chicago, Illinois, United States) A Alexis Tomlinson (Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States) I Isabella Farkas (Hospital of the University of Penn, Philadelphia, Pennsylvania, United States) J Jeanne Gottstsein (Northwestern University, Chicago, Illinois, United States) J Jack Rychik (Cardiology (D.J.G., J.R.), Children’s Hospital of Philadelphia, PA.) J Joanne Imperial (HepQuant LLC, Denver, Colorado, United States) M Michael McRae (HepQuant LLC, Denver, Colorado, United States) G Greg Everson (HepQuant LLC, Denver, Colorado, United States) M Maarouf Hoteit (Penn Medicine, Philadelphia, Pennsylvania, United States)

Abstract

Introduction: Fontan-associated liver disease [FALD] is universal in individuals with Fontan circulation [FC]. The dual cholate clearance test is a noninvasive, flow-dependent measure of liver function, and is abnormal in those with FC. We aim to explore the association between cholate clearance and clinical outcomes in this population. Hypothesis: Higher SHUNT% (systemic hepatic filtration rate [HFR]/portal HFR, an estimate of porto-systemic shunting) is associated with increased risk of death/transplant and is predictive of adverse clinical events. Methods: Two center prospective study of Fontan patients ≥ 18 years from University of Pennsylvania [Penn] and Northwestern University [NW]. Hepatic clearance of orally administered d4-cholate and intravenously administered 13C-cholate were measured in peripheral venous samples and calculated as portal HFR, systemic HFR, and SHUNT%. Primary outcome was transplant-free survival. Association between SHUNT% and transplant-free survival was assessed by Kaplan-Meier curves and the log-rank test for elevated SHUNT (>30%) and Cox regression for continuous SHUNT%. Secondary outcome was composite of death, transplant, new onset heart failure, ascites, protein losing enteropathy, or hepatocellular carcinoma. Logistic regression was used to evaluate the association between continuous SHUNT% and composite outcome. Sensitivity, specificity, and AUC were calculated. Results: Fifty participants (35 Penn, 15 NW) were enrolled. The Penn cohort was younger (median age 30 [IQR 25 – 37] vs 36 [IQR 30 – 41] years; p= 0.075) with shorter median follow-up (4.0 [IQR 3.4 – 4.8] vs 7.1 [IQR 5.0 – 8.9] years; p = 0.006). The composite outcome was reached in 14/50 (29%) including death (n=4), combined heart-liver transplant (n=4), or both (n=2). Unadjusted 1-year, 3-year, and 5-year transplant-free survival was 96%, 94%, and 79%, respectively. Figure 1 shows survival probability by SHUNT%. For every 10% incremental increase in SHUNT%, there was a 60% higher risk of death/transplant (95% CI 1.14 – 2.27; p = 0.006) and 70% higher odds of composite outcome (95% CI 1.05 – 3.03; p=0.045), adjusted for institution. SHUNT% >30% and institution identified those with composite outcome with sensitivity 64%, specificity 91%, and accuracy 83% (Figure 1). Conclusions: Higher SHUNT% is associated with lower transplant-free survival in individuals with FC and has modest discrimination in identifying those who experience future adverse clinical events.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (10)

Y

Yuli Kim

Hospital of the University of Penn, Philadelphia, Pennsylvania, United States

D

Daniel Ganger

Northwestern University, Chicago, Illinois, United States

A

Alexis Tomlinson

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States

I

Isabella Farkas

Hospital of the University of Penn, Philadelphia, Pennsylvania, United States

J

Jeanne Gottstsein

Northwestern University, Chicago, Illinois, United States

J

Jack Rychik

Cardiology (D.J.G., J.R.), Children’s Hospital of Philadelphia, PA.

J

Joanne Imperial

HepQuant LLC, Denver, Colorado, United States

M

Michael McRae

HepQuant LLC, Denver, Colorado, United States

G

Greg Everson

HepQuant LLC, Denver, Colorado, United States

M

Maarouf Hoteit

Penn Medicine, Philadelphia, Pennsylvania, United States