Liver stiffness predicts progression to liver‐related events in patients with chronic liver disease – A cohort study of 14 414 patients

Author:

Hegmar Hannes12ORCID,Wester Axel2ORCID,Aleman Soo3,Backman Jens4,Degerman Erik5,Ekvall Håkan6,Lund Katarina7,Lundgren Åsa8,Nasr Patrik29ORCID,Shahnavaz Afshin10,Vessby Johan11,Westin Johan12,Önnerhag Kristina13,Hagström Hannes12ORCID

Affiliation:

1. Division of Hepatology, Department of Upper GI Karolinska University Hospital Stockholm Sweden

2. Department of Medicine Huddinge, Karolinska Institutet Stockholm Sweden

3. Department of Infectious Diseases Karolinska University Hospital Stockholm Sweden

4. Department of Infectious Diseases University Hospital of Umeå Umeå Sweden

5. Department of Infectious Diseases Falun Hospital Falun Sweden

6. Department of Infectious Diseases Sundsvall‐Härnösand Regional Hospital Sundsvall Sweden

7. Department of Infectious Diseases Northern Älvsborg County Hospital Trollhättan Sweden

8. Department of Infectious Diseases Central Hospital Kristianstad Sweden

9. Department of Gastroenterology and Hepatology, Department of Health, Medicine and Caring Sciences Linköping University Linköping Sweden

10. Department of Infectious Diseases Södra Älvsborgs Hospital Borås Sweden

11. Department of Medical Sciences, Gastroenterology Research Group Uppsala University Uppsala Sweden

12. Department of Infectious Diseases Sahlgrenska University Hospital Gothenburg Sweden

13. Department of Gastroenterology and Hepatology Skåne University Hospital Malmö Sweden

Abstract

AbstractBackground & AimsLiver 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.MethodsThis 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.ResultsIncluded 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.ConclusionsIncreased 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.

Funder

Pfizer

Publisher

Wiley

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