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Liver stiffness predicts progression to liver-related events in patients with chronic liver disease - A cohort study of 14 414 patients. | LitMetric

AI Article Synopsis

  • Liver stiffness measurement (LSM) via vibration-controlled transient elastography (VCTE) is a key non-invasive indicator for assessing liver fibrosis, though its ability to predict future liver complications in diverse populations remains uncertain.
  • A study of 14,414 patients showed that higher LSM values significantly correlated with increased risks of developing cirrhosis and hepatocellular carcinoma (HCC), with over 28% of patients having high LSM (≥25 kPa) developing serious conditions.
  • The findings indicate that VCTE effectively predicts liver disease progression, supporting its use in clinical decision-making for monitoring and treating patients with chronic liver conditions.

Article Abstract

Background & Aims: Liver stiffness measurement (LSM) by vibration-controlled transient elastography (VCTE) is a non-invasive diagnostic biomarker of liver fibrosis. It is uncertain if LSM can predict risk for future liver-related outcomes in large, heterogenous populations.

Methods: This Swedish multi-centre cohort study included patients (n = 14 414) from 16 sites who underwent LSM by VCTE between 2008 and 2020. Outcomes were ascertained from national registers. We investigated progression to cirrhosis with portal hypertension or hepatocellular carcinoma (HCC), separately. Cox regression was used to obtain hazard ratios (HRs). Harrel's C-index was used to measure discrimination of VCTE.

Results: Included patients had a median age of 46 (interquartile range 34-57), median LSM of 5.9 kPa (4.6-8.0), 59% were male, and the majority had hepatitis C (50.1%). During a median follow-up of 5.9 (4.3-8.0) years, 402 patients (2.7%) developed cirrhosis with portal hypertension. In patients with an LSM ≥25 kPa, 28.7% developed cirrhosis with portal hypertension within 5 years of follow-up, while only .6% of patients with an LSM <10 kPa did. This translated to a HR of 48.3 (95% confidence interval = 37.6-62.0). VCTE had a high discriminative ability, with C-indices above .80 for most liver diseases, including .82 for MASLD. Similar findings were seen for incident HCC.

Conclusions: Increased LSM by VCTE was associated with an increased risk of progression to both cirrhosis with portal hypertension, and to HCC, and had a high discriminative ability across different aetiologies of chronic liver diseases. These results support the use of VCTE to guide follow-up and treatment decisions.

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Source
http://dx.doi.org/10.1111/liv.15919DOI Listing

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