Liver stiffness as a cornerstone in heart disease risk assessment

Author:

Boeckmans Joost12ORCID,Sandrin Laurent3ORCID,Knackstedt Christian45ORCID,Schattenberg Jörn M.16ORCID

Affiliation:

1. Metabolic Liver Research Center, I. Department of Medicine University Medical Center Mainz Mainz Germany

2. In Vitro Liver Disease Modelling Team, Department of In Vitro Toxicology and Dermato‐Cosmetology, Faculty of Medicine and Pharmacy Vrije Universiteit Brussel Brussels Belgium

3. Echosens Paris France

4. Department of Cardiology Maastricht University Medical Center+ Maastricht the Netherlands

5. Faculty of Health, Medicine, and Life Sciences CARIM School for Cardiovascular Diseases Maastricht the Netherlands

6. Department of Medicine II Saarland University Medical Center Homburg Germany

Abstract

AbstractMetabolic dysfunction‐associated steatotic liver disease (MASLD) typically presents with hepatic fibrosis in advanced disease, resulting in increased liver stiffness. A subset of patients further develops liver cirrhosis and hepatocellular carcinoma. Cardiovascular disease is a common comorbidity in patients with MASLD and its prevalence is increasing in parallel. Recent evidence suggests that especially liver stiffness, whether or not existing against a background of MASLD, is associated with heart diseases. We conducted a narrative review on the role of liver stiffness in the prediction of highly prevalent heart diseases including heart failure, cardiac arrhythmias (in particular atrial fibrillation), coronary heart disease, and aortic valve sclerosis. Research papers were retrieved from major scientific databases (PubMed, Web of Science) until September 2023 using ‘liver stiffness’ and ‘liver fibrosis’ as keywords along with the latter cardiac conditions. Increased liver stiffness, determined by vibration‐controlled transient elastography or hepatic fibrosis as predicted by biomarker panels, are associated with a variety of cardiovascular diseases, including heart failure, atrial fibrillation, and coronary heart disease. Elevated liver stiffness in patients with metabolic liver disease should lead to considerations of cardiac workup including N‐terminal pro–B‐type natriuretic peptide/B‐type natriuretic peptide determination, electrocardiography, and coronary computed tomography angiography. In addition, patients with MASLD would benefit from heart disease case‐finding strategies in which liver stiffness measurements can play a key role. In conclusion, increased liver stiffness should be a trigger to consider a cardiac workup in metabolically compromised patients.

Publisher

Wiley

Subject

Hepatology

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