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Inicio Annals of Hepatology P-13 EVALUATION OF UNDIAGNOSED ALCOHOLIC LIVER DISEASE IN PATIENTS WITH METABOLI...
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Vol. 29. Núm. S3.
Abstracts of the 2023 Annual Meeting of the ALEH
(diciembre 2024)
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Vol. 29. Núm. S3.
Abstracts of the 2023 Annual Meeting of the ALEH
(diciembre 2024)
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P-13 EVALUATION OF UNDIAGNOSED ALCOHOLIC LIVER DISEASE IN PATIENTS WITH METABOLIC DYSFUNCTION-ASSOCIATED FATTY LIVER DISEASE USING THE ANI SCORE
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Carlos Alventosa Mateu1, Mercedes Latorre Sánchez1, Inmaculada Castelló Miralles1, Benjamín Climent Díaz2, Juan José Urquijo Ponce1, Moisés Diago Madrid1
1 Hepatology Unit, Digestive Diseases Department, Consorcio Hospital General Universitario of Valencia, Valencia, España
2 Toxicology Unit, Internal Medicine Department, Consorcio Hospital General Universitario of Valencia, Valencia, España
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Vol. 29. Núm S3

Abstracts of the 2023 Annual Meeting of the ALEH

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Introduction and Objectives

The 2024 EASL-EASD-EASO guidelines on Steatotic Liver Disease emphasize the distinction between Metabolic Dysfunction-Associated Steatotic Liver Disease (MAFLD) and the subcategories with significant alcohol consumption: Alcoholic Liver Disease (ALD) and Metabolic ALD (MetALD). To this aim, a systematic record of alcohol consumption and/or validated biomarkers is recommended.

To evaluate the likelihood of associated but unrecognized alcohol-related liver disease (MetALD/ALD) in patients managed for MAFLD.

Patients / Materials and Methods

A single-center retrospective study that analyzes the probability of MetALD/ALD using the ALD/NAFLD (ANI) score in patients diagnosed with MAFLD during May/June 2024. MAFLD was defined by the presence of hepatic steatosis with alcohol intake <20/30 g/day (iwomen/men), at least one cardiovascular risk factor, and no other discernible cause. Patients with suspected advanced chronic liver disease were excluded. A probability of MetALD/ALD was considered if ANI>0 (indicative of a probability >50%). Sociodemographic variables, alcohol consumption, and hepatic fibrosis were recorded and compared between the ANI>0 and ANI<0 groups, with significance level set at p<0.05.

Results and Discussion

85 patients were included, average age 61.8±9.7 years, 52.9% male. Alcohol consumption was documented in medical history for 63.3% (54/85) of patients, with 53.4% (29/54) reporting no consumption. Per ANI score, 21.2% (18/85) were identified as having a probability of MetALD/ALD (ANI>0), with half of these (9/18) showing a probability >90%. Alcohol intake (10-20/30 g/day) was significantly higher in the ANI>0 group, consisting solely of males. Hepatic fibrosis was more pronounced in this group (7.6±3.6 vs 5.9±1.7) but did not reach statistical significance.

Conclusions

The significant prevalence of unrecognized MetALD/ALD by ANI score suggests that alcohol consumption may be underreported in the ANI>0 group. Therefore, the inclusion of the ANI score as a biomarker for accurate differentiation MAFLD from MetALD/ALD appears to be beneficial.

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Comparison of ANI>0 and ANI<0 groups.

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