Evidence map›Paper›PMID 39118031›Full record

SynthesisBMC psychiatry2024

Peripheral endocannabinoids in major depressive disorder and alcohol use disorder: a systematic review.

J J Fuentes, J Mayans, M Guarro, I Canosa, J I Mestre-Pintó, F Fonseca, M Torrens

Erratum issuedAbstract readSystematic Review
In one paragraph

Synthesis in BMC psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

J J FuentesMental Health Institute, Hospital del Mar, Barcelona, Spain.
J MayansDepartment of Psychiatry, Parc Sanitari Sant Joan de Déu, Sant Boi de Llobregat, Spain.
M GuarroMental Health Institute, Hospital del Mar, Barcelona, Spain.
I CanosaMental Health Institute, Hospital del Mar, Barcelona, Spain.
J I Mestre-PintóHospital del Mar Research Institute, Barcelona, Spain.
F FonsecaMental Health Institute, Hospital del Mar, Barcelona, Spain. mffonseca@psmar.cat.
M TorrensMental Health Institute, Hospital del Mar, Barcelona, Spain.

Funding

AGAUR-Gencat 2017 SGR 316, 2017 SGR 530Ministerio de Economía y Competitividad MTM2015-64465-C2-1-RRed de Investigación en Atención Primaria de Adicciones (RIAPAd) RD21/0009/0001
6 · The paper itself

Abstract

backgroundMajor Depressive Disorder (MDD) and Alcohol Use Disorder (AUD) are two high-prevalent conditions where the Endocannabinoid system (ECS) is believed to play an important role. The ECS regulates how different neurotransmitters interact in both disorders, which is crucial for controlling emotions and responses to stress and reward stimuli. Measuring peripheral endocannabinoids (eCBs) in human serum and plasma can help overcome the limitations of detecting endocannabinoid levels in the brain. This systematic review aims to identify levels of peripheral eCBs in patients with MDD and/or AUD and find eCBs to use as diagnostic, prognostic biomarkers, and potential therapeutic targets.

methodsWe conducted a systematic literature search according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines from the earliest manuscript until October 22, 2023, in three electronic databases. We included studies of human adults who had a current diagnosis of AUD and/or MDD and evaluated plasma or serum endocannabinoids. We carefully considered known variables that may affect endocannabinoid levels.

resultsWe included 17 articles in this systematic review, which measured peripheral eCBs in 170 AUD and 359 MDD patients. Stressors increase peripheral 2-arachidonyl-glycerol (2-AG) concentrations, and 2-AG may be a particular feature of depression severity and chronicity. Anxiety symptoms are negatively correlated with anandamide (AEA) concentrations, and AEA significantly increases during early abstinence in AUD. Studies suggest a negative correlation between Oleoylethanolamide (OEA) and length of abstinence in AUD patients. They also show a significant negative correlation between peripheral levels of AEA and OEA and fatty acid amide hydrolase (FAAH) activity. Eicosapentaenoylethanolamide (EPEA) is correlated to clinical remission rates in depression. Included studies show known variables such as gender, chronicity, symptom severity, comorbid psychiatric symptoms, length of abstinence in the case of AUD, and stress-inducibility that can affect peripheral eCBs.

conclusionsThis systematic review highlights the important role that the ECS plays in MDD and AUD. Peripheral eCBs appear to be useful biomarkers for these disorders, and further research may identify potential therapeutic targets. Using accessible biological samples such as blood in well-designed clinical studies is crucial to develop novel therapies for these disorders.

Indexed as

AlcoholismEndocannabinoidsMajor Depressive DisorderArachidonic AcidsBiomarkersGlyceridesHumansPolyunsaturated AlkamidesanandamideArachidonic AcidsBiomarkersEndocannabinoidsGlyceridesglyceryl 2-arachidonatePolyunsaturated AlkamidesAlcohol use disorderBiomarkersEndocannabinoidsMajor depressive disorder

Identifiers

PMID39118031
PMCPMC11308641

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.