Evidence map›Paper›PMID 26923505›Full record

ArticleBiological psychiatry2016

Interactions Between Anandamide and Corticotropin-Releasing Factor Signaling Modulate Human Amygdala Function and Risk for Anxiety Disorders: An Imaging Genetics Strategy for Modeling Molecular Interactions.

Catherine H Demers, Emily Drabant Conley, Ryan Bogdan, Ahmad R Hariri

Abstract read
In one paragraph

Article in Biological psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Biomarkers of stress resilience: A review.Neuroscience applied · 2024
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  4. Review
  5. Genes · 2023
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  11. Article
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  14. Article
  15. Article
  16. Article
  17. Integrating Endocannabinoid Signaling and Cannabinoids into the Biology and Treatment of Posttraumatic Stress Disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Review
  18. Article
  19. Article
  20. 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

4 authors at 3 institutions in 1 country.

Catherine H DemersPsychological and Brain Sciences, Washington University in St. Louis, St. Louis, Missouri.
Emily Drabant Conley23andMe, Inc., Mountain View, California.
Ryan BogdanPsychological and Brain Sciences, Washington University in St. Louis, St. Louis, Missouri; Division of Biology and Biomedical Sciences, Washington University in St. Louis, St. Louis, Missouri. Electronic address: rbogdan@wustl.edu.
Ahmad R HaririDepartment of Psychology and Neuroscience, Laboratory of NeuroGenetics, Duke University, Durham, North Carolina.
Washington University in St. Louis · US23andMe (United States) · USDuke University · US

Funding

Quantifying Individual Differences in Midlife Structural Brain Integrity Associated with Later AD/ADRD RiskR01AG049789 · NIA · DUKE UNIVERSITY · PI AHMAD R. HARIRI, TERRIE E MOFFITT · 2015 to 2026
$10.6M
Personality and Health in Later Life: Psychosocial and Biological MechanismsR01AG045231 · NIA · WASHINGTON UNIVERSITY · PI OLTMANNS, THOMAS · 2014 to 2018
$2.9M
T32 Training Grant in Epidemiology, Services and Prevention ResearchT32DA007313 · NIDA · WASHINGTON UNIVERSITY · PI PRICE, RUMI KATO · 1999 to 2013
$2.9M
Training At The Interface of Psychology, Neuroscience, and GeneticsT32GM081739 · NIGMS · WASHINGTON UNIVERSITY · PI BARCH, DEANNA · 2007 to 2016
$2.1M
Self-Regulation Failure: Identifying and Modifying a Risk PhenotypeR01DA031579 · NIDA · DUKE UNIVERSITY · PI HARIRI, AHMAD R., STRAUMAN, TIMOTHY J · 2010 to 2012
$1.9M
Neurogenetic Pathways to Drug Use in Young AdultsR01DA033369 · NIDA · DUKE UNIVERSITY · PI HARIRI, AHMAD R. · 2013 to 2016
$1.4M
NIA NIH HHS R01 AG045231NIA NIH HHS R01 AG049789NIDA NIH HHS R01 DA031579NIDA NIH HHS R01 DA033369NIDA NIH HHS T32 DA007313NIGMS NIH HHS T32 GM081739
6 · The paper itself

Abstract

backgroundPreclinical models reveal that stress-induced amygdala activity and impairment in fear extinction reflect reductions in anandamide driven by corticotropin-releasing factor receptor type 1 (CRF1) potentiation of the anandamide catabolic enzyme fatty acid amide hydrolase.

methodsHere, we provide clinical translation for the importance of these molecular interactions using an imaging genetics strategy to examine whether interactions between genetic polymorphisms associated with differential anandamide (FAAH rs324420) and CRF1 (CRHR1 rs110402) signaling modulate amygdala function and anxiety disorder diagnosis.

resultsAnalyses revealed that individuals with a genetic background predicting relatively high anandamide and CRF1 signaling exhibited blunted basolateral amygdala habituation, which further mediated increased risk for anxiety disorders among these same individuals.

conclusionsThe convergence of preclinical and clinical data suggests that interactions between anandamide and CRF1 represent a fundamental molecular mechanism regulating amygdala function and anxiety. Our results further highlight the potential of imaging genetics to powerfully translate complex preclinical findings to clinically meaningful human phenotypes.

Indexed as

AnxietyAmidohydrolasesAmygdalaArachidonic AcidsCorticotropin-Releasing HormoneCRF Receptor, Type 1EndocannabinoidsFatty Acid Amide HydrolasesFemaleGenotypeHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleOxygenPolymorphism, Single NucleotideAmidohydrolasesanandamideArachidonic AcidsCorticotropin-Releasing HormoneCRF Receptor, Type 1EndocannabinoidsFatty Acid Amide HydrolasesOxygenPolyunsaturated AlkamidesReceptors, Corticotropin-Releasing HormoneAmygdalaAnxietyCRHR1FAAHHabituationImaging genetics

Identifiers

PMID26923505
PMCPMC4935637
OpenAlexW2225107683

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.