Evidence map›Paper›PMID 40643612›Full record

ArticlePsychopharmacology2026

Relationships among peri-traumatic circulating endocannabinoids and long-term, negative outcomes following traumatic injury.

Emily A Albertina, Carissa W Tomas, Timothy J Geier, Sydney C Timmer-Murillo, Isela G Pina, Kelley Jazinski-Chambers, Garrett Sauber, Jacklynn M Fitzgerald, Christine L Larson, Terri A deRoon-Cassini and 1 more

Abstract read
In one paragraph

Article in Psychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Emily A AlbertinaDepartment of Psychology, University of Wisconsin, Milwaukee, USA. alberti8@uwm.edu.ORCID http://orcid.org/0000-0002-8681-558X
Carissa W TomasMedical College of Wisconsin Institute for Health and Equity, Division of Epidemiology and Social Sciences, Milwaukee, USA.
Timothy J GeierDivision of Trauma and Acute Care Surgery, Medical College of Wisconsin, Milwaukee, USA.
Sydney C Timmer-MurilloDivision of Trauma and Acute Care Surgery, Medical College of Wisconsin, Milwaukee, USA.
Isela G PinaDivision of Trauma and Acute Care Surgery, Medical College of Wisconsin, Milwaukee, USA.
Kelley Jazinski-ChambersDivision of Trauma and Acute Care Surgery, Medical College of Wisconsin, Milwaukee, USA.
Garrett SauberDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, USA.
Jacklynn M FitzgeraldDepartment of Psychology, Marquette University, Milwaukee, USA.
Christine L LarsonDepartment of Psychology, University of Wisconsin, Milwaukee, USA.
Terri A deRoon-Cassini *Medical College of Wisconsin Comprehensive Injury Center, Division of Data Surveillance & Informatics, Milwaukee, USA.
Cecilia J Hillard *Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, USA.

Funding

Acute Endocannabinoid activity involved in hyperarousal, memory formation, and non-remitting PTSD: A dense sampling approachR56MH116656 · NIMH · MEDICAL COLLEGE OF WISCONSIN · PI DEROON-CASSINI, TERRI A., HILLARD, CECILIA J · 2019 to 2019
$376k
NIMH NIH HHS R56 MH116656
6 · The paper itself

Abstract

rationaleTraumatically injured individuals can develop chronic negative psychological sequelae. Improved understanding of contributing, peri-traumatic risk factors is essential to reduce the risk of these consequences. Previous studies have found that peri-traumatic, circulating endocannabinoid concentrations are positively associated with development of post-traumatic stress disorder (PTSD), chronic pain and depression months later, particularly in members of racial/ethnic groups that have been historically marginalized.

objectivesThis replication study examined relationships among peri-trauma serum endocannabinoid concentrations and long-term consequences in a cohort comprised primarily of individuals from marginalized racial and ethnic groups.

methodsParticipants (n = 100; 81% from marginalized racial and ethnic groups) were traumatically injured adults presenting to the ED of an urban tertiary care hospital. Endocannabinoids N-arachidonoylethanolamine (AEA) and 2-arachidonoylglycerol (2-AG) were measured in serum collected within days (peri-trauma) and 6-10 months following injury (follow-up). Assessments, including PTSD, depression, pain and quality of life were completed. Statistical approaches, including multivariate, hierarchical regressions, were used to determine associations among serum endocannabinoid concentrations and long-term outcomes.

resultsAlthough it did not survive correction for multiple comparisons, peri-trauma serum 2-AG concentrations. Peri-trauma serum 2-AG concentrations were also positively associated with PTSD, pain severity, and functional engagement scores at follow-up. There were no significant associations between circulating 2-AG or AEA and depression.

conclusionsThese findings generally replicate earlier studies demonstrating that serum 2-AG concentrations are biomarkers of risk for PTSD and pain and uncover an additional association with poor functional quality of life. Further studies are needed to determine the underlying mechanisms of these relationships.

Indexed as

DepressionEndocannabinoidsGlyceridesStress Disorders, Post-TraumaticWounds and InjuriesAdultArachidonic AcidsChronic PainCohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedPolyunsaturated AlkamidesQuality of LifeArachidonic AcidsEndocannabinoidsGlyceridesglyceryl 2-arachidonatePolyunsaturated Alkamides2-ArachidonoylglycerolAnandamideCAPS-5Chronic painFunctional engagementPCL-5PTSDRacially/ethnically marginalized

Identifiers

PMID40643612
PMCPMC12904968

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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.