Evidence map›Paper›PMID 37626629›Full record

ArticleBiomedicines2023

New Diagnostic and Prognostic Models for the Development of Alcoholic Cirrhosis Based on Genetic Predisposition and Alcohol History.

Monica Mischitelli, Alessandra Spagnoli, Aurelio Abbatecola, Claudia Codazzo, Marta Giacomelli, Simona Parisse, Rosellina Margherita Mancina, Claudia Rotondo, Fabio Attilia, Stefano Ginanni Corradini and 1 more

Abstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Monica MischitelliDepartment of Translational and Precision Medicine, "Sapienza" University of Rome, Viale dell'Università 37, 00185 Rome, Italy.
Alessandra SpagnoliSection of BioMedical Statistics, Department of Public Health and Infectious Disease, Sapienza University, 00185 Rome, Italy.
Aurelio AbbatecolaDepartment of Translational and Precision Medicine, "Sapienza" University of Rome, Viale dell'Università 37, 00185 Rome, Italy.
Claudia CodazzoDepartment of Mental Health ASL RM1, UOSD CRARL, Sapienza University, 00186 Rome, Italy.
Marta GiacomelliDepartment of Translational and Precision Medicine, "Sapienza" University of Rome, Viale dell'Università 37, 00185 Rome, Italy.
Simona ParisseDepartment of Translational and Precision Medicine, "Sapienza" University of Rome, Viale dell'Università 37, 00185 Rome, Italy.ORCID 0000-0002-9953-009X
Rosellina Margherita MancinaWallenberg Laboratory, Department of Molecular and Clinical Medicine, Institute of Medicine, University of Gothenburg, 40530 Gothenburg, Sweden.ORCID 0000-0002-1126-3071
Claudia RotondoDepartment of Mental Health ASL RM1, UOSD CRARL, Sapienza University, 00186 Rome, Italy.
Fabio AttiliaDepartment of Mental Health ASL RM1, UOSD CRARL, Sapienza University, 00186 Rome, Italy.
Stefano Ginanni CorradiniDepartment of Translational and Precision Medicine, "Sapienza" University of Rome, Viale dell'Università 37, 00185 Rome, Italy.ORCID 0000-0002-0839-1961
Flaminia FerriDepartment of Translational and Precision Medicine, "Sapienza" University of Rome, Viale dell'Università 37, 00185 Rome, Italy.ORCID 0000-0001-8553-5589

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver cirrhosis development is a multifactorial process resulting from a combination of environmental and genetic factors. The aim of the study was to develop accurate non-invasive diagnostic and prognostic models for alcoholic cirrhosis. Consecutive subjects with at-risk alcohol intake were retrospectively enrolled (110 cirrhotic patients and 411 non-cirrhotics). At enrollment, the data about lifetime drinking history were collected and all patients were tested for Patatin-like phospholipase domain-containing protein 3 (PNPLA3) rs738409, Transmembrane 6 Superfamily 2 (TM6SF2) rs58542926, and hydroxysteroid 17-beta dehydrogenase 13 (HSD17B13) rs72613567 variants. In cross-sectional analyses, models for the diagnosis of cirrhosis were developed using multivariate logistic regression. A predictive score for cirrhosis development over 24 years was built by evaluating time-dependent AUC curves. The best diagnostic accuracy was demonstrated by the model, which also includes daily alcohol consumption, duration of hazardous alcohol use, and genetic variants, with AUCs of 0.951 (95% CI 0.925-0.977) and 0.887 (95% CI 0.925-0.977) for cirrhosis and compensated cirrhosis, respectively. The predictive model for future cirrhosis development (AUC of 0.836 95% CI: 0.769-0.904) accounted for age at onset of at-risk alcohol consumption and the number of PNPLA3 and HSD17B13 variant alleles. We have developed accurate genetic and alcohol consumption models for the diagnosis of alcoholic cirrhosis and the prediction of its future risk.

Indexed as

alcoholic liver diseasecirrhosis diagnosiscirrhosis predictiongeneticsHSD17B13PNPLA3

Identifiers

PMID37626629
PMCPMC10452718

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