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Published on: November 7, 2020
YKL-40: Revolutionizing cardiac risk prediction and therapy in liver transplantation
Ileana Lulic1,2, Dinka Lulic3,4, Ivan Durekovic1
1Department of Anesthesiology, Intensive Care and Pain Medicine, Clinical Hospital Merkur, Zagreb 10000, Croatia.
Insights
YKL-40, a biomarker, shows promise in predicting cardiovascular risks for liver transplant (LT) patients. Integrating YKL-40 into risk models can improve patient selection and care.
Area of Science:
- Biomedical research
- Cardiovascular medicine
- Transplantation science
Background:
- Cardiovascular complications are a major cause of death in liver transplantation (LT).
- Current risk assessment strategies for LT patients have limitations.
- YKL-40, a glycoprotein, is linked to inflammation, endothelial dysfunction, and fibrosis.
Abstract:
Cardiovascular complications remain a leading cause of morbidity and mortality in liver transplantation (LT), exposing the limitations of current risk assessment strategies. YKL-40, a glycoprotein involved in inflammation, endothelial dysfunction, and fibrotic remodeling, has emerged as a biomarker associated with adverse cardiovascular outcomes and liver disease severity. Its inclusion in structured cardiovascular assessment frameworks may improve transplant-specific risk scores and support earlier identification of high-risk LT recipients. Mechanistically, YKL-40 contributes to vascular injury and myocardial dysfunction via nuclear factor-κB and STAT3 signaling, and is under investigation as a biomarker in preclinical studies aimed at cardiovascular risk modulation in LT. Integration of YKL-40 into predictive models, particularly those supported by artificial intelligence, may enhance individualized perioperative decision-making. This editorial outlines translational directions for integrating YKL-40 into cardiovascular risk models and therapeutic research, supporting its clinical adoption in precision-guided LT care.
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