| Title: | Development, validation, and prognostic evaluation of LiverPRO for the prediction of significant liver fibrosis in primary care: a prospective cohort study |
| Journal: | The Lancet Gastroenterology & Hepatology |
| Published: | 1 Jan 2025 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/39674225/ |
| DOI: | https://doi.org/10.1016/s2468-1253(24)00274-7 |
Publication 13721
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Abstract
BACKGROUND: Clinically significant liver fibrosis is associated with future adverse events in patients with steatotic liver disease. We designed a software tool for detection of clinically significant liver fibrosis in primary care.</p>
METHODS: In this prospective cohort study, we developed and validated LiverPRO using six independent cohorts from Denmark, Germany, and England that included patients from primary and secondary care with steatotic liver disease related to alcohol or metabolic dysfunction. We used clinically significant fibrosis (histology stage ≥F2) and advanced fibrosis (≥F3) as outcomes for variable selection in the development cohort and built the model with fractional polynomial regression. In all cohorts, we independently validated the tool for prediction of elevated liver stiffness by transient elastography (≥8 kPa and ≥12 kPa) and for the 2-year and 5-year risk of liver-related events. Diagnostic performance was assessed using the area under the receiver operating curve (AUC), with clinical performance evaluated through sensitivity, specificity, and Harrell's C-statistic for prognostic purposes.</p>
FINDINGS: In the development cohort (n=462), we derived 466 multivariable models consisting of age in combination with three to nine variables from a list of nine blood tests (aspartate aminotransferase, alkaline phosphatase, gamma-glutamyl transferase, international normalised ratio, albumin, sodium, bilirubin, platelet count, and cholesterol). In the development cohort, LiverPRO diagnosed clinically significant fibrosis with good accuracy (transient elastography ≥8 kPa area under the receiver operating characteristic curve [AUC] 0·86 [95% CI 0·83-0·90]). In the DECIDE validation cohort (n=6468), LiverPRO detected participants with a transient elastography of 8 kPa or higher with good accuracy (AUC 0·80 [95% CI 0·78-0·82]), comparable to enhanced liver fibrosis testing (0·78 [0·75-0·80]) and the LiverRisk score (0·81 [0·79-0·84]), but superior to the Fibrosis-4 index (0·69 [0·66-0·72]) and NAFLD Fibrosis Score (0·74 [0·72-0·77]). Findings were consistent in three other validation cohorts (n=2554), albeit accuracy was slightly lower. Using a rule-out cutoff of less than 25% (indicating no further examinations required), LiverPRO had a rule-out sensitivity of 80·6% (95% CI 76·4-84·3) and a rule-out negative predictive value of 98·0% (95% CI 97·5-98·4) in the DECIDE cohort. Similarly, with a rule-out cutoff of less than 1·3, FIB-4 had a rule-out sensitivity of 53·8% (48·5-58·9) and a rule-out negative predictive value of 95·8% (95·1-96·4). For rule-in thresholds, using a cutoff of more than 65% (indicating referral to a hepatologist required) LiverPRO had a rule-in specificity of 95·5% (95% CI 94·9-96·0) and a rule-in positive predictive value of 33·0% (95% CI 28·5-37·8) in the DECIDE cohort whereas FIB-4, with a rule-in threshold of 2·67, had a rule-in specificity of 98·7% (94·9-96·0) and a rule-in positive predictive value 35·6% (27·0-44·9). Using UK Biobank data, LiverPRO predicted liver-related events with a C-statistic of 0·80 (0·77-0·84) at 2 years.</p>
INTERPRETATION: LiverPRO reliably identifies clinically significant liver fibrosis and elevated liver stiffness, predicts the risk of liver-related events in primary care, and is adaptable to the availability of different liver blood test analytes. On the basis of these results LiverPRO was certified according to IVDR class b, obtaining European CE approval in 2024.</p>
FUNDING: EU Horizon 2020 research and innovation programme and Novo Nordisk Foundation.</p>
20 Keywords
- Adult
- Aged
- Aspartate Aminotransferases
- Cohort Studies
- Denmark
- Elasticity Imaging Techniques
- England
- Fatty Liver
- Female
- Germany
- Humans
- Liver Cirrhosis
- Male
- Middle Aged
- Platelet Count
- Predictive Value of Tests
- Primary Health Care
- Prognosis
- Prospective Studies
- ROC Curve
30 Authors
- Katrine P Lindvig
- Katrine H Thorhauge
- Johanne K Hansen
- Maria Kjærgaard
- Camilla D Hansen
- Stine Johansen
- Ellen Lyngbeck
- Mads Israelsen
- Peter Andersen
- Katrine T Bech
- Nikolaj Torp
- Helle L Schnefeld
- Sönke Detlefsen
- Sören Möller
- Isabel Graupera
- Morten B Trelle
- Steen Antonsen
- Rebecca Harris
- Line L Kårhus
- Kirsten S Bjørnsbo
- Charlotte Brøns
- Torben Hansen
- Andreas Geier
- Heiner Wedemeyer
- Stefan Zeuzem
- Jörn M Schattenberg
- Pere Ginès
- Indra Neil Guha
- Aleksander Krag
- Maja Thiele
1 Application
| Application ID | Title |
|---|---|
| 94859 | THE LIVERPRO SCORE, A MULTIVARIABLE MODEL FOR PREDICTION OF SIGNIFICANT FIBROSIS IN PRIMARY CARE: DEVELOPMENT, VALIDATION AND COMPARISON WITH NON-INVASIVE FIBROSIS TESTS |
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