Evidence map›Paper›PMID 36536364›Full record

ArticleBMC psychiatry2022

Efficacy of eicosapentaenoic acid in inflammatory depression: study protocol for a match-mismatch trial.

Klara Suneson, Filip Ängeby, Jesper Lindahl, Gustav Söderberg, Johanna Tjernberg, Daniel Lindqvist

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMC psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03143075 (Do Omega-3 Fatty Acids Have an Antidepressant Effect in Patients With Signs of Peripheral Inflammation?), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 57% 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.

NCT03143075 nacompletednot on this map

Do Omega-3 Fatty Acids Have an Antidepressant Effect in Patients With Signs of Peripheral Inflammation?

TypeinterventionalSponsorRegion SkaneRan2017 to 2023Enrolled95ConditionsMajor Depressive DisorderArmsEicosapentaenoic acid enriched omega-3 fatty acids, 2 g/day
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

6 authors at 1 institution in 1 country.

Klara SunesonDepartment of Clinical Sciences Lund, Psychiatry, Faculty of Medicine, Lund University, 221 85, Lund, Sweden. klara.suneson@med.lu.se.ORCID 0000-0002-7104-1892
Filip ÄngebyOffice for Psychiatry and Habilitation, Psychiatric Clinic Lund, Region Skåne, 221 85, Lund, Sweden.
Jesper LindahlDepartment of Clinical Sciences Lund, Psychiatry, Faculty of Medicine, Lund University, 221 85, Lund, Sweden.
Gustav SöderbergDepartment of Clinical Sciences Lund, Psychiatry, Faculty of Medicine, Lund University, 221 85, Lund, Sweden.
Johanna TjernbergDepartment of Clinical Sciences Lund, Psychiatry, Faculty of Medicine, Lund University, 221 85, Lund, Sweden.
Daniel LindqvistDepartment of Clinical Sciences Lund, Psychiatry, Faculty of Medicine, Lund University, 221 85, Lund, Sweden.
Lund University · SE

Funding

Vetenskapsrådet 2020-01428
6 · The paper itself

Abstract

backgroundMost antidepressant treatment studies have included patients strictly based on the Diagnostic and Statistical Manual of Mental Disorders definition of Major Depressive Disorder (MDD). Given the heterogeneity of MDD, this approach may have obscured inter-patient differences and hampered the development of novel and targeted treatment strategies. An alternative strategy is ​​to use biomarkers to delineate endophenotypes of depression and test if these can be targeted via mechanism-based interventions. Several lines of evidence suggest that "inflammatory depression" is a clinically meaningful subtype of depression. Preliminary data indicate that omega-3 fatty acids, with their anti-inflammatory and neuroprotective properties, may be efficacious in this subtype of depression, and this study aims to test this hypothesis.

methodWe conduct a match-mismatch-trial to test if add-on omega-3 fatty acid eicosapentaenoic acid (EPA) reduces depressive symptoms in patients with MDD and systemic low-grade inflammation. MDD patients on a stable antidepressant treatment are stratified at baseline on high sensitivity-C-reactive protein (hs-CRP) levels to a high-inflammation group (hs-CRP ≥ 3 mg/L) or a low-inflammation group (hs-CRP < 3 mg/L). Both groups receive add-on EPA (2 g per day) for 8 weeks with three study visits, all including blood draws. Patients and raters are blind to inflammation status. Primary outcome measure is change in Hamilton Depression Rating Scale score between baseline and week 8. We hypothesize that the inflammation group has a superior antidepressant response to EPA compared to the non-inflammation group. Secondary outcomes include a composite score of "inflammatory depressive symptoms", quality of life, anxiety, anhedonia, sleep disturbances, fatigue, cognitive performance and change in biomarkers relating to inflammation, oxidative stress, metabolomics and cellular aging. DISCUSSION: In this study we will, for the first time using a match-mismatch trial design, test if omega-3 is an efficacious treatment for inflammatory depression. If our study is successful, it could add to the field of precision psychiatry.

trial registrationThis trial was registered May 8, 2017 on clinicaltrials.gov under the reference number NCT03143075.

Indexed as

Eicosapentaenoic AcidMajor Depressive DisorderAntidepressive AgentsBiomarkersC-Reactive ProteinDepressionDouble-Blind MethodHumansInflammationQuality of LifeTreatment OutcomeAntidepressive AgentsBiomarkersC-Reactive ProteinEicosapentaenoic AcidInflammationMajor Depressive DisorderN-3 PUFA

Identifiers

PMID36536364
PMCPMC9761617
OpenAlexW4312113223

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.