Evidence map›Paper›PMID 32860939›Full record

ArticleBrain, behavior, and immunity2020

Differential effect of interferon-alpha treatment on AEA and 2-AG levels.

Zuzanna Zajkowska, Alessandra Borsini, Naghmeh Nikkheslat, Alice Russell, Graziella F Romano, Simona Tomassi, Nilay Hepgul, Daniel Forton, Kosh Agarwal, Matthew Hotopf and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Brain, behavior, and immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
0.4field-weighted citation impact, top 49% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. 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

13 authors at 4 institutions in 1 country.

Zuzanna ZajkowskaDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK. Electronic address: Zuzanna.zajkowska@kcl.ac.uk.
Alessandra BorsiniDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK.
Naghmeh NikkheslatDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK.
Alice RussellDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK.
Graziella F RomanoDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK.
Simona TomassiDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK.
Nilay HepgulDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK.
Daniel FortonDepartment of Gastroenterology & Hepatology, St George's University of London, UK.
Kosh AgarwalInstitute of Liver Studies, King's College Hospital, UK.
Matthew HotopfDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK; National Institute for Health Research (NIHR), Mental Health Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London, UK.
Valeria MondelliDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK; National Institute for Health Research (NIHR), Mental Health Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London, UK.
Patricia ZunszainDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK.
Carmine M ParianteDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, UK; National Institute for Health Research (NIHR), Mental Health Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London, UK.
King's College London · GBKing's College Hospital · GBNational Institute for Health Research · GBSt George's, University of London · GB

Funding

Medical Research Council G108/603Medical Research Council MR/J002739/1Medical Research Council MR/N029488/1Wellcome Trust
6 · The paper itself

Abstract

The endocannabinoid (eCB) system is one of the key players in immunoregulation, and reduced activity of the eCB system has been linked with depressive-like behaviours in animal studies and depression in clinical samples. There is a well-established link between immune activation and depression, such as following the administration of the pro-inflammatory cytokine, interferon-α (IFN-α), used to treat hepatitis C viral (HCV) infection. However, the role of peripheral endocannabinoids (eCBs), anandamide (AEA) and 2-arachidonoylglycerol (2-AG), following immunotherapy with IFN-α and in IFN-α -induced depression, have not been examined yet. In this study, we investigated whether circulating AEA and 2-AG were modified by treatment with IFN-α and whether they were involved in the development of IFN-α-induced depression. We also explored whether circulating eCBs were associated with peripheral cytokines during and after IFN-α treatment. We measured serum concentrations of AEA and 2-AG using High Performance Liquid Chromatography with Tandem Mass Spectrometry, and serum concentrations of cytokines using Meso Scale Discovery electrochemiluminescence V-PLEX assay, in 70 patients with HCV infection and 41 healthy subjects. We assessed HCV patients at baseline, IFN-α-treatment weeks (TW) 4 and 24, end of treatment (END) and at six months follow-up (FU). We assessed depression using M.I.N.I. International Neuropsychiatric Interview. We found a different pattern of change in peripheral AEA and 2-AG during and after IFN-α treatment. Whilst 2-AG increased earlier in immunotherapy (TW4), remained elevated throughout treatment, and reduced at six months follow-up (FU), AEA increased later in treatment (TW24) and remained elevated six months post-treatment. We also found that baseline levels of AEA were lower in HCV patients compared with healthy controls, whereas there were no differences in 2-AG levels. Interestingly, AEA, but not 2-AG, was significantly, negatively correlated with interleukin (IL)-2 and IL-17a at six months follow-up. We did not find any difference in both eCBs between patients with and without IFN-α-induced depression, at any time point. Our findings suggest that AEA and 2-AG are involved in different stages of immunoregulation following IFN-α treatment, where AEA might be involved in chronic inflammation. Lack of association between peripheral eCBs and IFN-α-induced depression suggests that different biological mechanisms may underpin inflammation-induced depression compared with classic "psychiatric" depression, or that any changes in the eCB system in depression may not be captured by peripheral AEA and 2-AG.

Indexed as

Interferon-alphaSilverAnimalsCytokinesEndocannabinoidsHumansInflammationCytokinesEndocannabinoidsInterferon-alphaSilver2-Aracgidonoylglycerol (2-AG)Anandamide (AEA)CytokinesDepressionEndocannabinoid systemHepatitis CIFN-α-induced depressionImmune systemInflammationInterferon-α (IFN-α)

Identifiers

PMID32860939
PMCPMC7575143
OpenAlexW3080980191

What OpenQuestion holds

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LicenceCC BY
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.