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Sakura Horie, Fumiaki Shikata, Norihiko Oka, Toru Okamura, Yoshikiyo Matsunaga, Kenta Matsui, Tsutomu Hataoka, Tadashi Kitamura, Masaomi Fukuzumi, Ryoichi Kondo, Yoichiro Hirata, Kagami Miyaji, Liver fibrosis marker is a potential predictor of the development of Fontan-associated liver diseases, European Journal of Cardio-Thoracic Surgery, Volume 67, Issue 4, April 2025, ezaf100, https://doi.org/10.1093/ejcts/ezaf100
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Abstract
To evaluate how well liver fibrosis markers (fibrosis-4 index, aspartate aminotransferase to platelet ratio index, and model for end-stage liver disease excluding international normalized ratio score) can predict early detection of Fontan-associated liver disease and to identify risk factors for Fontan-associated liver disease development.
This retrospective multicentre study included patients who underwent the Fontan procedure between 2004 and 2020 with at least 3 years of follow-up. Blood tests and imaging were conducted to diagnose Fontan-associated liver disease. The predictive value of these markers was assessed using receiver operating characteristic curve analysis. Risk factors for Fontan-associated liver disease development were identified using Fine–Gray subdistribution hazard analysis.
This study included 137 patients. The fibrosis-4 index, measured at 2 years post-Fontan, was a strong predictor for Fontan-associated liver disease development 10 years later (area under the curve: 0.81, optimal cutoff value: 0.17, 83.1% sensitivity, and 73.0% specificity). Fine–Gray subdistribution hazard analysis shows that a fibrosis-4 index level was a key risk factor for Fontan-associated liver disease. Patients with a fibrosis-4 index >0.17 after 2 years had a higher incidence of Fontan-associated liver disease after 10 years (45.6%) than patients with fibrosis-4 index ≤0.17 (3.9%, P = 0.002). These patients also had higher pulmonary artery pressure 5 years later.
The fibrosis-4 may be a useful marker for early detection of Fontan-associated liver disease, which, in this study, was identified as a risk factor for the disease’s development.
Kitasato University, No. B23-130; 7 February 2024.