Evidence map›Paper›PMID 41521699›Full record

ArticleLiver international : official journal of the International Association for the Study of the Liver2026

Genetic Information Enhances a Novel Non-Invasive Steatosis Index and Outperforms Existing Steatosis Indices.

Yousif Alyousifi, Chinmay Raut, Vincent L Chen, Antonino Oliveri, Yanhua Chen, Elizabeth K Speliotes

Abstract read
In one paragraph

Article in Liver international : official journal of the International Association for the Study of the Liver, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Yousif AlyousifiDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-1530-4317
Chinmay RautDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-0663-383X
Vincent L ChenDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-0157-6066
Antonino OliveriDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0003-2621-6443
Yanhua ChenDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Elizabeth K SpeliotesDivision of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Funding

Integrative Polygenic Genetic Studies of Non-alcoholic Fatty Liver DiseaseR01DK131787 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SPELIOTES, ELIZABETH K · 2022 to 2025
$2.7M
Identification and Characterization of Loci Associated with Non-alcoholic Fatty Liver DiseaseR01DK128871 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALLRED, NICHOLETTE D., SPELIOTES, ELIZABETH K · 2021 to 2024
$2.6M
Multi Ancestry Whole Genome Sequencing Analyses of MASLD with Functional Follow UpR01DK141823 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Nicholette D. Allred, Elizabeth K Speliotes · 2025 to 2026
$1.5M
Predictive models for incident cirrhosis in non-alcoholic fatty liver disease using genetic and electronic medical record-based risk factorsK08DK132312 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Vincent Lingzhi Chen · 2022 to 2026
$834k
NIDDK NIH HHS K08 DK132312NIDDK NIH HHS R01 DK128871NIDDK NIH HHS R01 DK131787NIDDK NIH HHS R01 DK141823
6 · The paper itself

Abstract

BACKGROUND AND

aimsEarly detection of individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) is important as interventions to reduce steatosis can prevent progression to advanced liver disease. Identification of individuals with hepatic steatosis relies on imaging techniques, which are costly and often unavailable in large populations. Identifying hepatic steatosis through blood tests and demographics may serve as a cost-effective alternative to identifying hepatic steatosis. Here, we aim to identify demographic, serum and genetic variables that can help predict hepatic steatosis in two large population-based cohorts.

methodsWe analysed data from 32 008 participants in the UK Biobank (UKBB) with liver fat quantified using magnetic resonance proton density fat fraction (MRI-PDFF). We created non-invasive models to predict steatosis, the Enhanced Steatosis Indexes (ESIs), using logistic regression. Candidate predictors included variables from the literature and genetic markers. ESI-1 variables included demographic and serum values. ESI-2 included the ESI-1 variables plus the genetic markers. We trained and tested these models in UKBB and validated them in the Framingham Heart Study (FHS).

resultsIn UKBB, ESI-1 and ESI-2 predicted ≥ 5% PDFF with AUC 0.844 and 0.858, respectively, outperforming DSI, HSI, FSI and FLI (AUC 0.818-0.834 vs. ESI-1 and AUC 0.830-0.844 vs. ESI-2). In FHS, ESI-1 and ESI-2 predicted CT-measured liver steatosis with AUC 0.803 and 0.808, respectively.

conclusionsWe developed a non-invasive model to diagnose steatosis that outperforms existing steatosis models. Including genetic information improved the performance of ESI-2. Deployment of our models can facilitate non-invasive screening of steatosis so that, with early intervention, disease progression can be prevented. IMPACT AND IMPLICATIONS: We developed a non-invasive model based on demographic, serum laboratory and genetic predictors that outperforms existing steatosis indices in identifying individuals with hepatic steatosis. This Enhanced Steatosis Index (ESI) enables more accurate and personalised early detection of hepatic steatosis, a highly prevalent yet underdiagnosed condition. By leveraging readily available clinical measures and genetic data, both ESI-1 and ESI-2 improve risk stratification and support large-scale screening and early intervention efforts. These advances have the potential to provide more affordable, accurate and targeted screening, facilitating earlier treatment, reducing the burden of metabolic liver disease and helping to address disparities in the diagnosis and management of hepatic steatosis.

Indexed as

Fatty LiverNon-alcoholic Fatty Liver DiseaseAgedBiomarkersEarly DiagnosisFemaleGenetic MarkersHumansLiverLogistic ModelsMagnetic Resonance ImagingMaleMiddle AgedUK BiobankUnited KingdomBiomarkersGenetic Markersblood testhepatic steatosisliver steatosismachine learningnon‐invasive scorepolygenic risk score

Identifiers

PMID41521699
PMCPMC13434854

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.