Evidence map›Paper›PMID 33723218›Full record

ArticleTranslational psychiatry2021

Predicting alcohol use disorder remission: a longitudinal multimodal multi-featured machine learning approach.

Sivan Kinreich, Vivia V McCutcheon, Fazil Aliev, Jacquelyn L Meyers, Chella Kamarajan, Ashwini K Pandey, David B Chorlian, Jian Zhang, Weipeng Kuang, Gayathri Pandey and 14 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% of its field
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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

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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

24 authors at 7 institutions in 2 countries.

Sivan KinreichDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA. sivan.kinreich@downstate.edu.ORCID 0000-0001-6480-1622
Vivia V McCutcheonDepartment of Psychiatry, Washington University School of Medicine in St Louis, St Louis, MO, USA.
Fazil AlievDepartment of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0001-8357-4699
Jacquelyn L MeyersDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.ORCID 0000-0003-3863-8555
Chella KamarajanDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.ORCID 0000-0003-2291-6880
Ashwini K PandeyDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.ORCID 0000-0002-2688-7901
David B ChorlianDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.
Jian ZhangDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.
Weipeng KuangDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.
Gayathri PandeyDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.
Stacey Subbie-Saenz de ViteriDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.
Meredith W FrancisBrown School of Social Work / Department of Psychiatry, Washington University in Saint Louis, St. Louis, MO, USA.
Grace ChanDepartment of Psychiatry, University of Connecticut School of Medicine, Farmington, CT, USA.ORCID 0000-0002-1257-6889
Jessica L BourdonDepartment of Psychiatry, Washington University School of Medicine in St Louis, St Louis, MO, USA.ORCID 0000-0002-7291-1431
Danielle M DickDepartment of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.ORCID 0000-0002-1636-893X
Andrey P AnokhinDepartment of Psychiatry, Washington University School of Medicine in St Louis, St Louis, MO, USA.
Lance BauerDepartment of Psychiatry, University of Connecticut School of Medicine, Farmington, CT, USA.
Victor HesselbrockDepartment of Psychiatry, University of Connecticut School of Medicine, Farmington, CT, USA.
Marc A SchuckitDepartment of Psychiatry, University of California, San Diego School of Medicine, La Jolla, CA, USA.
John I NurnbergerDepartments of Psychiatry and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID 0000-0002-7674-1767
Tatiana M ForoudDepartment of Medical and Molecular Genetics at Indiana University School of Medicine, Indianapolis, IN, USA.
Jessica E SalvatoreDepartment of Psychology, Virginia Commonwealth University, Richmond, VA, USA.
Kathleen K BucholzDepartment of Psychiatry, Washington University School of Medicine in St Louis, St Louis, MO, USA.
Bernice PorjeszDepartment of Psychiatry, State University of New York, Downstate Medical Center, Brooklyn, NY, USA.
State University of New York · USWashington University in St. Louis · USUniversity of Connecticut · USIndiana University School of MedicineVirginia Commonwealth University · USKarabük University · TRUniversity of California San Diego · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JAY Arnold TISCHFIELD · 1989 to 2026
$162.7M
Transdisciplinary Training in Addictions ResearchT32DA015035 · NIDA · WASHINGTON UNIVERSITY · PI Leopoldo J Cabassa, Patricia A Cavazos-Rehg · 2002 to 2026
$5.3M
DEVELOPMENT OF A COGNITIVE SCREENING BATTERY FOR AGEDR43AG008401 · NIA · POWELL ASSOCIATES · PI WURGAFT, LEWIS D · 1989 to 1989
–
NIAAA NIH HHS U10 AA008401NIDA NIH HHS T32 DA015035
6 · The paper itself

Abstract

Predictive models for recovering from alcohol use disorder (AUD) and identifying related predisposition biomarkers can have a tremendous impact on addiction treatment outcomes and cost reduction. Our sample (N = 1376) included individuals of European (EA) and African (AA) ancestry from the Collaborative Study on the Genetics of Alcoholism (COGA) who were initially assessed as having AUD (DSM-5) and reassessed years later as either having AUD or in remission. To predict this difference in AUD recovery status, we analyzed the initial data using multimodal, multi-features machine learning applications including EEG source-level functional brain connectivity, Polygenic Risk Scores (PRS), medications, and demographic information. Sex and ancestry age-matched stratified analyses were performed with supervised linear Support Vector Machine application and were calculated twice, once when the ancestry was defined by self-report and once defined by genetic data. Multifeatured prediction models achieved higher accuracy scores than models based on a single domain and higher scores in male models when the ancestry was based on genetic data. The AA male group model with PRS, EEG functional connectivity, marital and employment status features achieved the highest accuracy of 86.04%. Several discriminative features were identified, including collections of PRS related to neuroticism, depression, aggression, years of education, and alcohol consumption phenotypes. Other discriminated features included being married, employed, medication, lower default mode network and fusiform connectivity, and higher insula connectivity. Results highlight the importance of increasing genetic homogeneity of analyzed groups, identifying sex, and ancestry-specific features to increase prediction scores revealing biomarkers related to AUD remission.

Indexed as

AlcoholismAlcohol DrinkingBrainHumansMachine LearningMaleSupport Vector Machine

Identifiers

PMID33723218
PMCPMC7960734
OpenAlexW3136951845

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.