Evidence map›Paper›PMID 42704308›Full record

ArticleAlcohol, clinical & experimental research2026

Classification of Alcohol Use Disorder With Explainable AI.

Alexander S Hatoum, Alex P Miller, Hunter L Mathews, Aaron J Gorelik, David A A Baranger, Zhen Luo, Jodi Kutzer, Emma C Johnson, Arpana Agrawal, Ryan Bogdan

Abstract read
In one paragraph

Article in Alcohol, clinical & experimental research, 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

10 authors.

Alexander S HatoumDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID https://orcid.org/0000-0002-8002-7267
Alex P MillerDepartment of Psychiatry, Indiana University School of Medicine, Bloomington, Indiana, USA.ORCID https://orcid.org/0000-0001-9163-8947
Hunter L MathewsDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID https://orcid.org/0000-0001-8564-7783
Aaron J GorelikDepartment of Psychological & Brain Sciences, Washington Univeristy in Saint Louis, St. Louis, Missouri, USA.ORCID https://orcid.org/0000-0002-2589-1220
David A A BarangerDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Zhen LuoDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri, USA.
Jodi KutzerDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri, USA.
Emma C JohnsonDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID https://orcid.org/0000-0003-0394-777X
Arpana AgrawalDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri, USA.
Ryan BogdanDepartment of Psychological & Brain Sciences, Washington Univeristy in Saint Louis, St. Louis, Missouri, USA.

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JAY Arnold TISCHFIELD · 1989 to 2026
$162.7M
7/7 Psychiatric Genomics Consortium: Advancing Discovery and ImpactR01DA054869 · NIDA · WASHINGTON UNIVERSITY · PI AGRAWAL, ARPANA, EDENBERG, HOWARD J · 2021 to 2025
$3.3M
Mass Multivariate Derivation and Validation of AUD Biotypes using Developmental Imaging and Genomic ApproachesK01AA030083 · NIAAA · WASHINGTON UNIVERSITY · PI Alexander S Hatoum · 2022 to 2026
$897k
Identifying genetic sources of comorbidity between cannabis and schizophrenia using genome-wide and integrative omics dataK01DA051759 · NIDA · WASHINGTON UNIVERSITY · PI JOHNSON, EMMA COVEY · 2021 to 2025
$816k
Neurogenetic influences linking impulsive personality traits and alcohol use disorder progression across developmentK01AA031724 · NIAAA · INDIANA UNIVERSITY INDIANAPOLIS · PI Alex Parker Miller · 2024 to 2026
$548k
Reciprocal longitudinal associations between brain function and alcohol use trajectories in adolescents and young adultsR00AA030808 · NIAAA · MEDICAL COLLEGE OF WISCONSIN · PI David A Baranger · 2025 to 2026
$498k
Reciprocal longitudinal associations between brain function and alcohol use trajectories in adolescents and young adultsK99AA030808 · NIAAA · WASHINGTON UNIVERSITY · PI BARANGER, DAVID A · 2023 to 2024
$346k
NIAAA NIH HHS AA008401NIAAA NIH HHS AA030083NIAAA NIH HHS AA030808NIAAA NIH HHS AA031724NIAAA NIH HHS K01 AA030083NIAAA NIH HHS K01 AA031724NIAAA NIH HHS K99 AA030808NIAAA NIH HHS R00 AA030808NIAAA NIH HHS U10 AA008401NIDA NIH HHS DA051759NIDA NIH HHS DA054869NIDA NIH HHS K01 DA051759NIDA NIH HHS R01 DA054869
6 · The paper itself

Abstract

backgroundThe wide-ranging correlates (e.g., demographic, socioeconomic status [SES], brain, genetics) of alcohol use disorder (AUD) are typically characterized by small effects and studied in isolation. Novel multivariable nonlinear approaches may help characterize the multifaceted correlates of AUD and identify its strongest predictors.

methodHere, using Gradient Boosted Machines (GBMs), we classify AUD in the UK Biobank (N = 12,178) from features (n = 440) within the following 5 domains: (1) demographic (n = 12), (2) socioeconomic status (n = 18), (3) non-substance mental health (n = 55), (4) non-alcohol substance involvement (n = 6), and (5) biological features (n = 342). We use Explainable Artificial Intelligence (xAI) to characterize each respective feature's contribution to model performance and its heterogeneity, as well as the extent to which features from each domain collectively contribute to model performance.

resultsIn an out-of-sample hold-out test set (n = 6089), our model classified lifetime AUD well (AUC = 0.80). Notably, feature importance analyses revealed that demographic (age, sex, income), substance use (ever smoke tobacco or ever use cannabis), and mental health questionnaires (social isolation) were most informative to classifying AUD. The gradient boosted machine significantly outperformed a linear model and implicated non-zero pairwise interactions among variables, suggesting potential heterogeneity of AUD presentation by income and sex. Further, incrementally incorporating neuroimaging and genetic data as features led to small but consistent improvement in classifying AUD, with small effect sizes distributed across a number of variables (0%-2% gain based on overall model classification). This suggests the continued importance of biological features in classifying AUD beyond psychological and demographic measures, though classification with single selected brain regions may be limited.

conclusionMultimodal multivariable approaches considering nonlinear relationships may improve our understanding of AUD correlates. Particularly, accounting for interactions with demographic factors and integrating information across biological features may enhance model performance.

Indexed as

AlcoholismArtificial IntelligenceAgedBoosting Machine Learning AlgorithmsClassification AlgorithmsFemaleHumansMaleMiddle AgedUK BiobankUnited Kingdomalcohol use disorderexplainable AIgeneticmachine learningneuroimaging

Identifiers

PMID42704308
PMCPMC13549157

What OpenQuestion holds

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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.