Evidence map›Paper›PMID 37115410›Full record

ArticleAlcohol, clinical & experimental research2023

Evidence for an alcohol-related "harm paradox" in individuals with internalizing disorders: Test and replication in two independent community samples.

Justin J Anker, Paul Thuras, Ruichong Shuai, Lee Hogarth, Matt G Kushner

Open access · hybridAbstract read
In one paragraph

Article in Alcohol, clinical & experimental research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 6 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

5 authors at 3 institutions in 2 countries.

Justin J AnkerDepartment of Psychiatry and Behavioral Sciences, University of Minnesota - Minneapolis, Minneapolis, Minnesota, USA.ORCID 0000-0002-2115-5170
Paul ThurasMinneapolis VA Medical Center, Minneapolis, Minneapolis, Minnesota, USA.
Ruichong ShuaiSchool of Psychology, University of Exeter, Exeter, UK.ORCID 0000-0002-7178-3423
Lee HogarthSchool of Psychology, University of Exeter, Exeter, UK.
Matt G KushnerDepartment of Psychiatry and Behavioral Sciences, University of Minnesota - Minneapolis, Minneapolis, Minnesota, USA.ORCID 0000-0002-8506-2053
University of Exeter · GBUniversity of Minnesota · USMinneapolis VA Medical Center · US

Funding

Validating an Autonomous Interactive Internet-Based Delivery of an Empirically Supported Cognitive Behavioral Therapy for ComorbidityR01AA029077 · NIAAA · UNIVERSITY OF MINNESOTA · PI KUSHNER, MATT G · 2021 to 2025
$2.2M
Physiological Stress Reactivity as a Determinant in Co-occurring Alcohol Use and Anxiety Disorder: Diagnosis and Alcohol Use OutcomesK01AA024805 · NIAAA · UNIVERSITY OF MINNESOTA · PI ANKER, JUSTIN JACK · 2017 to 2021
$726k
NIAAA NIH HHS K01 AA024805NIAAA NIH HHS R01 AA029077
6 · The paper itself

Abstract

backgroundInternalizing (anxiety and mood) disorders (INTD) commonly co-occur (are "comorbid") with alcohol use disorder (AUD). The literature suggests that excessive alcohol use aimed at coping with INTD symptoms is, at best, a partial explanation for the high comorbidity rates observed. We hypothesized that individuals with INTD experience greater susceptibility to developing AUD symptoms due to the partially shared neurobiological dysfunctions underlying both conditions. We probe this hypothesis by testing the prediction that, after accounting for the volume of alcohol intake, individuals with INTD experience higher levels of alcohol-related symptoms.

methodsData from the National Epidemiological Survey on Alcohol-Related Conditions (NESARC) Wave 3 were used for the primary analyses, and NESARC Wave 1 data were used for independent replication analyses. Individuals who reported any alcohol use in the prior year were categorized as: (1) never having had an INTD diagnosis ("INTD-Never"); (2) having a remitted INTD diagnosis only ("INTD-Remitted"); or (3) having current INTD diagnosis ("INTD-Current"). Between-group contrasts of alcohol-related symptoms controlled for total alcohol intake (past year), drinking pattern (e.g., binging) and variables previously shown to mark exaggerated AUD symptoms relative to drinking amount (e.g., SES, gender, and family history).

resultsWith all covariates in the model, individuals in the INTD-Current group and the INTD-Remitted group reported significantly greater alcohol-related symptoms than those in the INTD-Never group but did not themselves differ in level of alcohol-related symptoms. These results were replicated in the NESARC 1 dataset.

conclusionsIndividuals with INTD experience more alcohol-related symptoms than those who drink at the same level. While considering other explanations, we argue that this "harm paradox" is best explained by the view that INTD confers a neurobiologically mediated susceptibility to the development of AUD symptoms.

Indexed as

AlcoholismAlcohol-Related DisordersAlcohol DrinkingAnxiety DisordersComorbidityHumansalcohol use disorderanxiety disordercomorbiditydepressionNESARC

Identifiers

PMID37115410
PMCPMC10416809
OpenAlexW4367311485

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.