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Progression of liver fibrosis and liver-related event risk in MASLD at high cardiovascular risk

Progression of liver fibrosis and liver-related event risk in MASLD at high cardiovascular risk
Progression of liver fibrosis and liver-related event risk in MASLD at high cardiovascular risk
Background & aims: patients with metabolic dysfunction-associated steatotic liver disease (MASLD) and high cardiovascular risk often have advanced liver fibrosis, but data on associations and outcomes are limited. The aim of this study was to evaluate the relationships between cardiovascular risk categories and liver fibrosis severity, liver fibrosis progression, and liver-related events (LREs) in MASLD.

Methods: patients with MASLD from the VCTE-Prognosis cohort were stratified into low, intermediate, and high cardiovascular risk categories using the Framingham Risk Score (FRS), Primary Care Equivalents (PCE), or Predicting Risk of Cardiovascular Disease EVENTs (PREVENT) scores. Outcomes included the prevalence of advanced fibrosis (liver stiffness ≥10 kPa), liver stiffness progression (≥20% increase and Baveno category upshift), and LRE (hepatocellular carcinoma, hepatic decompensation, liver transplantation, or liver-related mortality). Associations were assessed using multivariable logistic regression and Fine-Gray competing-risks models.

Results: among 9312 patients with MASLD (mean age, 54.4 ± 11.0 years; 56.8% male; 87.4% Asian), advanced fibrosis prevalence increased with cardiovascular risk: adjusted odds ratios (ORs) were 2.72 (95% confidence interval [CI], 2.25–3.28; P < .001) for FRS, 1.83 (95% CI, 1.46–2.29; P < .001) for PCE, and 2.93 (95% CI, 2.33–3.69; P < .001) for PREVENT. Over a median follow-up of 4.5 years, liver stiffness progression occurred in 5.0% of patients, more frequently in high-risk groups (adjusted subdistribution hazard ratio [SHR], 1.56; 95% CI, 1.14–2.15; P = .006 for PCE and adjusted SHR, 1.85; 95% CI, 1.33–2.56; P < .001 for PREVENT). LREs occurred in 1.4% of patients, with higher incidence in high-risk groups (adjusted SHR, 2.12; 95% CI, 1.19–3.77; P = .010 for FRS; adjusted SHR, 2.01; 95% CI, 1.08–3.74; P = .027 for PCE; and adjusted SHR, 2.80; 95% CI, 1.40–5.61; P = .004 for PREVENT).

Conclusions: higher cardiovascular risk is associated with greater prevalence of advanced liver fibrosis, liver stiffness progression, and LRE incidence in MASLD.

1542-3565
Zhou, Xiao-Dong
8a33ecdb-a642-40cd-b64c-d1bc6bcb3efb
Chen, Qin-Fen
e486ccf6-db17-4094-89dd-ac2607b4a320
Kim, Seung Up
82515251-999b-4a89-b388-6aaa6931745e
Byrne, Chrisopher D.
1370b997-cead-4229-83a7-53301ed2a43c
et al.
Zhou, Xiao-Dong
8a33ecdb-a642-40cd-b64c-d1bc6bcb3efb
Chen, Qin-Fen
e486ccf6-db17-4094-89dd-ac2607b4a320
Kim, Seung Up
82515251-999b-4a89-b388-6aaa6931745e
Byrne, Chrisopher D.
1370b997-cead-4229-83a7-53301ed2a43c

et al. (2026) Progression of liver fibrosis and liver-related event risk in MASLD at high cardiovascular risk. Clinical Gastroenterology and Hepatology. (doi:10.1016/j.cgh.2026.01.038).

Record type: Article

Abstract

Background & aims: patients with metabolic dysfunction-associated steatotic liver disease (MASLD) and high cardiovascular risk often have advanced liver fibrosis, but data on associations and outcomes are limited. The aim of this study was to evaluate the relationships between cardiovascular risk categories and liver fibrosis severity, liver fibrosis progression, and liver-related events (LREs) in MASLD.

Methods: patients with MASLD from the VCTE-Prognosis cohort were stratified into low, intermediate, and high cardiovascular risk categories using the Framingham Risk Score (FRS), Primary Care Equivalents (PCE), or Predicting Risk of Cardiovascular Disease EVENTs (PREVENT) scores. Outcomes included the prevalence of advanced fibrosis (liver stiffness ≥10 kPa), liver stiffness progression (≥20% increase and Baveno category upshift), and LRE (hepatocellular carcinoma, hepatic decompensation, liver transplantation, or liver-related mortality). Associations were assessed using multivariable logistic regression and Fine-Gray competing-risks models.

Results: among 9312 patients with MASLD (mean age, 54.4 ± 11.0 years; 56.8% male; 87.4% Asian), advanced fibrosis prevalence increased with cardiovascular risk: adjusted odds ratios (ORs) were 2.72 (95% confidence interval [CI], 2.25–3.28; P < .001) for FRS, 1.83 (95% CI, 1.46–2.29; P < .001) for PCE, and 2.93 (95% CI, 2.33–3.69; P < .001) for PREVENT. Over a median follow-up of 4.5 years, liver stiffness progression occurred in 5.0% of patients, more frequently in high-risk groups (adjusted subdistribution hazard ratio [SHR], 1.56; 95% CI, 1.14–2.15; P = .006 for PCE and adjusted SHR, 1.85; 95% CI, 1.33–2.56; P < .001 for PREVENT). LREs occurred in 1.4% of patients, with higher incidence in high-risk groups (adjusted SHR, 2.12; 95% CI, 1.19–3.77; P = .010 for FRS; adjusted SHR, 2.01; 95% CI, 1.08–3.74; P = .027 for PCE; and adjusted SHR, 2.80; 95% CI, 1.40–5.61; P = .004 for PREVENT).

Conclusions: higher cardiovascular risk is associated with greater prevalence of advanced liver fibrosis, liver stiffness progression, and LRE incidence in MASLD.

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More information

Accepted/In Press date: 24 January 2026
e-pub ahead of print date: 6 February 2026

Identifiers

Local EPrints ID: 510645
URI: http://eprints.soton.ac.uk/id/eprint/510645
ISSN: 1542-3565
PURE UUID: 4164b3d4-af8d-4029-b19d-cc1ed8aa0de0
ORCID for Chrisopher D. Byrne: ORCID iD orcid.org/0000-0001-6322-7753

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Date deposited: 15 Apr 2026 16:34
Last modified: 18 Apr 2026 01:38

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Contributors

Author: Xiao-Dong Zhou
Author: Qin-Fen Chen
Author: Seung Up Kim
Corporate Author: et al.

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