1322-P: Combination of LiverSTAT (LST) and Fibroscan (LSM) Outperforms FIB-4 and LSM for MASLD Advanced Fibrosis (AF) F3F4
Background: LiverSTAT (LST) is a new blood test for MASLD stratification. Aims: To retrospectively compare the efficacy of two combinations in one-step approach with two combinations: LST&LSM versus FIB-4&LSM, for the identification of advanced fibrosis (F3F4) in a multicenter multiethnic me...
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Published in | Diabetes (New York, N.Y.) Vol. 73; no. Supplement_1; p. 1 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
American Diabetes Association
14.06.2024
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Subjects | |
Online Access | Get full text |
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Summary: | Background: LiverSTAT (LST) is a new blood test for MASLD stratification.
Aims: To retrospectively compare the efficacy of two combinations in one-step approach with two combinations: LST&LSM versus FIB-4&LSM, for the identification of advanced fibrosis (F3F4) in a multicenter multiethnic meta-dataset of MASLD patients.
Methods: Retrospective data from 5 hepatology centers from MASLD patients that underwent liver biopsy (LB) along with LSM, FIB-4 and LST. Efficiency has been assessed using concordance rates, number needed to screen (NNS) on subject with LB F3F4.
Results: Data from 786 patients (22%US, 39%Asia, 39%EU) was analyzed [age 57.1years, female 54.5%, BMI 31.4, ALT 52U/L]. LB prevalence of F3F4 was 32.8%.In the overall cohort, LB confirmed F3F4 among concordant LST&LSM and FIB-4&LSM, respectively, in 107/142(75%) vs 54/64(84.4%) with a screening efficiency (NNS) of 1.8 vs 2.2; the combination LST&LSM correctly identified twice more F3F4 patients than FIB-4&LSM.In the subgroup with LB≥20mm, LB confirmed F3F4 among concordant LST&LSM and FIB-4&LSM in 43/50(86%) vs 30/33(90%), NNS 1.6 and 1.8, respectively; the combination LST&LSM correctly identified 43% more F3F4 patients than FIB-4&LSM.DFP rate was higher with FIB4-&LSM than with LST&LSM (11.3% vs. 7%).
Conclusion: The combination LST&LSM outperforms FIB-4&LSM for the identification of MASH advanced fibrosis F3F4. |
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Bibliography: | ObjectType-Conference Proceeding-1 SourceType-Scholarly Journals-1 content type line 14 |
ISSN: | 0012-1797 1939-327X |
DOI: | 10.2337/db24-1322-P |