Evidence map›Paper›PMID 30291441›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2019

Impact of FAAH genetic variation on fronto-amygdala function during emotional processing.

Anne Gärtner, Denise Dörfel, Kersten Diers, Stephanie H Witt, Alexander Strobel, Burkhard Brocke

Abstract read
PubMed Publisher
In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Short- and long-term effects of emotion up- and down-regulation.Imaging neuroscience (Cambridge, Mass.) · 2023
    Article
  7. FAAH polymorphism (rs324420) modulates extinction recall in healthy humans: an fMRI study.European archives of psychiatry and clinical neuroscience · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. The contributions of the endocannabinoid system and stress on the neural processing of reward stimuli.Progress in neuro-psychopharmacology & biological psychiatry · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. A Guide to Targeting the Endocannabinoid System in Drug Design.International journal of molecular sciences · 2020
    Review
  18. Article
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Anne GärtnerFaculty of Psychology, Technische Universität Dresden, Dresden, Germany. anne_gaertner@tu-dresden.de.
Denise DörfelFaculty of Psychology, Technische Universität Dresden, Dresden, Germany.
Kersten DiersFaculty of Psychology, Technische Universität Dresden, Dresden, Germany.
Stephanie H WittDepartment of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Alexander StrobelFaculty of Psychology, Technische Universität Dresden, Dresden, Germany.
Burkhard BrockeFaculty of Psychology, Technische Universität Dresden, Dresden, Germany.
TU Dresden · DECentral Institute of Mental Health · DE

Funding

Deutsche Forschungsgemeinschaft SFB 940
6 · The paper itself

Abstract

Recent translational studies identified a common endocannabinoid polymorphism, FAAH C385A, in the gene for the fatty acid amide hydrolase (FAAH). This polymorphism alters endocannabinoid anandamide levels, which are known to be involved in the fronto-amygdala circuitry implicated in mood regulation and anxiety-like behaviors. While it has been shown that the variant that selectively enhances fronto-amygdala connectivity at rest is associated with decreased anxiety-like behaviors, no study so far has investigated whether this finding of FAAH-related differential plasticity extends to task-related differential functional expression and regulation during negative emotional processing. Using an imaging genetics approach, this study aimed to replicate and extend prior findings by examining functional activity and task-related connectivity in fronto-amygdala regions during emotion reactivity and emotional down-regulation of negative affect. Therefore, 48 healthy young adults underwent a functional MRI resting state measurement, completed an emotion regulation paradigm and provided self-reports on anxiety and use of emotion regulation strategies. In line with previous studies, preliminary evidence suggests that A-allele carriers demonstrate stronger fronto-amygdala connectivity during rest. In addition, exploratory whole-brain analyses indicate differential functional activity of A-allele carriers during emotion reactivity and emotion regulation. There were no associations with anxiety-related self-reports and use of emotional regulation strategies. Further research using larger samples and polygenic approaches is indicated to clarify the precise role and its underlying mechanisms in emotion processing.

Indexed as

AnxietyAdolescentAdultAmidohydrolasesAmygdalaConnectomeEmotionsFatty Acid Amide HydrolasesFemaleGenotypeHumansMagnetic Resonance ImagingMalePrefrontal CortexYoung AdultAmidohydrolasesFatty Acid Amide HydrolasesAmygdalaEmotion reactivityEmotion regulationFAAH C385AfMRIFronto-amygdalaFunctional connectivityGeneticsIndividual differences

Identifiers

PMID30291441
OpenAlexW2895210437

What OpenQuestion holds

Textmetadata
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.