Evidence map›Paper›PMID 40474763›Full record

Observational studyAlcohol, clinical & experimental research2025

The reciprocal relationship between posttraumatic stress disorder symptoms and alcohol use in a large multisite longitudinal sample stratified by sex: A random-intercept cross-lagged panel model.

Cecilia A Hinojosa, Sanne J H van Rooij, Negar Fani, Robyn A Ellis, Henri M Garrison-Desany, Stacey L House, Francesca L Beaudoin, Xinming An, Thomas C Neylan, Gari D Clifford and 8 more

Abstract readComparative StudyMulticenter StudyObservational Study
In one paragraph

Observational study in Alcohol, clinical & experimental research, 2025. 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

18 authors.

Cecilia A HinojosaDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0002-2577-6142
Sanne J H van RooijDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia, USA.
Negar FaniDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia, USA.
Robyn A EllisDivision of Alcohol, Drugs, & Addiction, McLean Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Henri M Garrison-DesanyDepartment of Social and Behavioral Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Stacey L HouseDepartment of Emergency Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Francesca L BeaudoinDepartment of Epidemiology, Brown University, Providence, Rhode Island, USA.
Xinming AnInstitute for Trauma Recovery, Department of Anesthesiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Thomas C NeylanDepartment of Psychiatry, University of California San Francisco, San Francisco, California, USA.
Gari D CliffordDepartment of Biomedical Informatics, Emory University School of Medicine, Atlanta, Georgia, USA.
Sarah D LinnstaedtInstitute for Trauma Recovery, Department of Anesthesiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Laura T GermineInstitute for Technology in Psychiatry, McLean Hospital, Belmont, Massachusetts, USA.
Scott L RauchInstitute for Technology in Psychiatry, McLean Hospital, Belmont, Massachusetts, USA.
AURORA Study Group
Karestan C KoenenDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Harvard University, Boston, Massachusetts, USA.
Kerry J ResslerDepartment of Psychiatry, Harvard Medical School, Boston, Massachusetts, USA.
Samuel A McLeanDepartment of Emergency Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Jennifer S StevensDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, Georgia, USA.

Funding

Longitudinal Assessment of Post-traumatic SyndromesU01MH110925 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KESSLER, RONALD C, KOENEN, KARESTAN C · 2016 to 2020
$25.8M
Clinical Features and Neuropathological Basis of Sleep Wake Behavior in Alzheimer's and PSPR01AG060477 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Lea Tenenholz Grinberg, Thomas C Neylan · 2019 to 2026
$8.2M
Investigating Fear System Myelination in PTSD Using In Vivo and Post Mortem DataR01MH132617 · NIMH · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI HUBER, BERTRAND R, NEYLAN, THOMAS C · 2023 to 2025
$2.1M
MAYDAY FundNIA NIH HHS R01 AG060477NIH HHS U01MH110925NIMH NIH HHS R01 MH132617NIMH NIH HHS U01 MH110925US Army Medical Research and Material CommanUS Army Medical Research and Material Command
6 · The paper itself

Abstract

backgroundPosttraumatic stress disorder (PTSD) and alcohol use disorder (AUD) often co-occur. There is a lack of longitudinal studies measuring the naturalistic development of PTSD and alcohol use problems in individuals with recent trauma exposure. This study aimed to compare the temporal relationships between posttraumatic stress symptoms and alcohol use over 6 months following trauma exposure in males and females.

methodsLarge-scale longitudinal observational emergency department (ED)-based study of individuals with recent trauma exposure. Individuals with recent trauma exposure (n = 2942, 62% female) were recruited from 29 EDs across the United States within 72 h of trauma exposure from 2017 to 2021. PTSD symptoms, measured via the PTSD Checklist for the DSM-5, and alcohol use measured via the PhenX toolkit, were assessed at five time points: ED visit, 2 weeks, 8 weeks, 3 months, and 6 months following trauma.

resultsPTSD symptoms predicted lower future alcohol use between the pretrauma to two-week time points (b = -0.08, p = 0.01) and higher use between the 3- to 6-month time points (b = 0.06, p = 0.01). There were no time points in which alcohol use predicted future PTSD symptoms. When stratifying by sex, male participants showed reciprocal associations, with alcohol use early after trauma predicting PTSD symptoms between 2 and 8 weeks (b = 0.08, p = 0.01), while PTSD symptoms predicted alcohol use between the 3- to 6-month time points (b = 0.10, p = 0.01). Female participants showed a different reciprocal pattern, with pretrauma PTSD symptoms predicting lower alcohol use 2 weeks posttrauma (b = -0.08, p = 0.04), while alcohol use subsequently predicted greater PTSD symptoms from 8 weeks to 3 months (b = 0.04, p = 0.04); these findings did not survive Bonferroni correction.

conclusionsMales and females exhibit complex temporal development patterns of PTSD symptoms and alcohol use that align with the mutual maintenance hypothesis in males but the susceptibility hypothesis in females. These patterns are masked in analyses that do not stratify by sex.

Indexed as

Alcohol DrinkingAlcoholismStress Disorders, Post-TraumaticAdultEmergency Service, HospitalFemaleHumansLongitudinal StudiesMaleMiddle AgedSex FactorsUnited StatesYoung Adultalcohol drinkingbiological sexemergency departmentposttraumatic stress disorderrandom‐intercept cross‐lagged panel modeltrauma

Identifiers

PMID40474763
PMCPMC12997135

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.