Evidence map›Paper›PMID 25162199›Full record

ArticleJAMA psychiatry2014

Interaction of the ADRB2 gene polymorphism with childhood trauma in predicting adult symptoms of posttraumatic stress disorder.

Israel Liberzon, Anthony P King, Kerry J Ressler, Lynn M Almli, Peng Zhang, Sean T Ma, Gregory H Cohen, Marijo B Tamburrino, Joseph R Calabrese, Sandro Galea

Abstract read
In one paragraph

Article in JAMA psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 4 pooled it
4.8field-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

45 citing papers in PubMed, 4 syntheses or guidelines pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Locus coeruleus: a new look at the blue spot.Nature reviews. Neuroscience · 2020
    Review
  19. Review
  20. βAnnual review of pharmacology and toxicology · 2020
    Review
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 at 7 institutions in 1 country.

Israel LiberzonDepartment of Psychiatry, University of Michigan, Ann Arbor2Veterans Affairs Ann Arbor Health System, Ann Arbor, Michigan.
Anthony P KingDepartment of Psychiatry, University of Michigan, Ann Arbor2Veterans Affairs Ann Arbor Health System, Ann Arbor, Michigan.
Kerry J ResslerEmory University, Atlanta, Georgia.
Lynn M AlmliEmory University, Atlanta, Georgia.
Peng ZhangThe Johns Hopkins University, Baltimore, Maryland.
Sean T MaDepartment of Psychiatry, University of Michigan, Ann Arbor.
Gregory H CohenColumbia University, New York, New York.
Marijo B TamburrinoUniversity of Toledo, Toledo, Ohio.
Joseph R CalabreseCase Western University, Cleveland, Ohio.
Sandro GaleaColumbia University, New York, New York.
Columbia University · USEmory University · USUniversity of Michigan–Ann Arbor · USJohns Hopkins University · USUniversity of Toledo · USVA Ann Arbor Healthcare System · USWestern University of Health Sciences · US

Funding

Genetic and Trauma-Related Risk Factors for PTSDR01MH071537 · NIMH · EMORY UNIVERSITY · PI RESSLER, KERRY J. · 2005 to 2014
$8.5M
NIMH NIH HHS R01 MH071537
6 · The paper itself

Abstract

importancePosttraumatic stress disorder (PTSD), while highly prevalent (7.6% over a lifetime), develops only in a subset of trauma-exposed individuals. Genetic risk factors in interaction with trauma exposure have been implicated in PTSD vulnerability.

objectiveTo examine the association of 3755 candidate gene single-nucleotide polymorphisms with PTSD development in interaction with a history of childhood trauma. DESIGN, SETTING, AND

participantsGenetic association study in an Ohio National Guard longitudinal cohort (n = 810) of predominantly male soldiers of European ancestry, with replication in an independent Grady Trauma Project (Atlanta, Georgia) cohort (n = 2083) of predominantly female African American civilians. MAIN OUTCOMES AND MEASURES: Continuous measures of PTSD severity, with a modified (interview) PTSD checklist in the discovery cohort and the PTSD Symptom Scale in the replication cohort.

resultsControlling for the level of lifetime adult trauma exposure, we identified the novel association of a single-nucleotide polymorphism within the promoter region of the ADRB2 (Online Mendelian Inheritance in Man 109690) gene with PTSD symptoms in interaction with childhood trauma (rs2400707, P = 1.02 × 10-5, significant after correction for multiple comparisons). The rs2400707 A allele was associated with relative resilience to childhood adversity. An rs2400707 × childhood trauma interaction predicting adult PTSD symptoms was replicated in the independent predominantly female African American cohort. CONCLUSIONS AND RELEVANCE: Altered adrenergic and noradrenergic function has been long believed to have a key etiologic role in PTSD development; however, direct evidence of this link has been missing. The rs2400707 polymorphism has been linked to function of the adrenergic system, but, to our knowledge, this is the first study to date linking the ADRB2 gene to PTSD or any psychiatric disorders. These findings have important implications for PTSD etiology, chronic pain, and stress-related comorbidity, as well as for both primary prevention and treatment strategies.

Indexed as

AdolescentAdultAllelesChild AbuseFemaleGenome-Wide Association StudyGenotyping TechniquesHumansMaleMiddle AgedPolymorphism, Single NucleotideReceptors, Adrenergic, beta-2Stress Disorders, Post-TraumaticYoung AdultADRB2 protein, humanReceptors, Adrenergic, beta-2

Identifiers

PMID25162199
PMCPMC4597911
OpenAlexW2127201367

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.