Evidence map›Paper›PMID 25802980›Full record

Trial reportMolecular psychiatry2016

Inflammation as a predictive biomarker for response to omega-3 fatty acids in major depressive disorder: a proof-of-concept study.

M H Rapaport, A A Nierenberg, P J Schettler, B Kinkead, A Cardoos, R Walker, D Mischoulon

2 registry-linked trialsOpen access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Molecular psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 136 papers, 15 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
136citing papers in PubMed, 15 pooled it
8.6field-weighted citation impact, top 1% 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.

NCT02553915 phase2 / phase3completednot on this map

Omega-3 Fatty Acids for MDD With High Inflammation: A Personalized Approach

TypeinterventionalSponsorMassachusetts General HospitalRan2015 to 2022Enrolled61ConditionsMajor Depressive Disorder, Overweight, InflammationArmsPlacebo, EPA 1 g/day, EPA 2 g/day, EPA 4 g/day
NCT03143075 nacompletednot on this mapstarted 2017, after this paper: background citation

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

136 citing papers in PubMed, 15 syntheses or guidelines pooled it, 263 citations in OpenAlex.

  1. Pooled it
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  3. Nutraceuticals in Psychiatric Disorders: A Systematic Review.International journal of molecular sciences · 2024
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  5. Omega-3 fatty acids for depression in adults.The Cochrane database of systematic reviews · 2021
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  13. Efficacy of omega-3 highly unsaturated fatty acids in the treatment of depression.The British journal of psychiatry : the journal of mental science · 2016
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  15. Omega-3 fatty acids for depression in adults.The Cochrane database of systematic reviews · 2015
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76 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

M H RapaportDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
A A NierenbergDepression Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
P J SchettlerDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
B KinkeadDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
A CardoosDepression Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
R WalkerDepression Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
D MischoulonDepression Clinical and Research Program, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Emory University · USHarvard University · USMassachusetts General Hospital · US

Funding

Omega-3 Fatty Acids for Treatment of Major DepressionR01MH074085 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI MISCHOULON, DAVID · 2006 to 2010
$1.7M
Omega-3 Fatty Acids for Treatment of Major Depressive DisorderR01MH073765 · NIMH · CEDARS-SINAI MEDICAL CENTER · PI COHEN, ROBERT MARTIN · 2006 to 2010
$1.7M
NIMH NIH HHS 5R01MH74085NIMH NIH HHS R01 MH073765NIMH NIH HHS R01 MH074085
6 · The paper itself

Abstract

This study explores whether inflammatory biomarkers act as moderators of clinical response to omega-3 (n-3) fatty acids in subjects with major depressive disorder (MDD). One hundred fifty-five subjects with Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV) MDD, a baseline 17-item Hamilton Depression Rating Scale (HAM-D-17) score ⩾ 15 and baseline biomarker data (interleukin (IL)-1ra, IL-6, high-sensitivity C-reactive protein (hs-CRP), leptin and adiponectin) were randomized between 18 May 2006 and 30 June 2011 to 8 weeks of double-blind treatment with eicosapentaenoic acid (EPA)-enriched n-3 1060 mg day(-1), docosahexaenoic acid (DHA)-enriched n-3 900 mg day(-1) or placebo. Outcomes were determined using mixed model repeated measures analysis for 'high' and 'low' inflammation groups based on individual and combined biomarkers. Results are presented in terms of standardized treatment effect size (ES) for change in HAM-D-17 from baseline to treatment week 8. Although overall treatment group differences were negligible (ES=-0.13 to +0.04), subjects with any 'high' inflammation improved more on EPA than placebo (ES=-0.39) or DHA (ES=-0.60) and less on DHA than placebo (ES=+0.21); furthermore, EPA-placebo separation increased with increasing numbers of markers of high inflammation. Subjects randomized to EPA with 'high' IL-1ra or hs-CRP or low adiponectin ('high' inflammation) had medium ES decreases in HAM-D-17 scores vs subjects 'low' on these biomarkers. Subjects with 'high' hs-CRP, IL-6 or leptin were less placebo-responsive than subjects with low levels of these biomarkers (medium to large ES differences). Employing multiple markers of inflammation facilitated identification of a more homogeneous cohort of subjects with MDD responding to EPA vs placebo in our cohort. Studies are needed to replicate and extend this proof-of-concept work.

Indexed as

AdultAgedBiomarkersC-Reactive ProteinDietary SupplementsDocosahexaenoic AcidsDouble-Blind MethodEicosapentaenoic AcidFemaleHumansInterleukin 1 Receptor Antagonist ProteinInterleukin-6LeptinMajor Depressive DisorderMaleMiddle AgedBiomarkersC-Reactive ProteinDocosahexaenoic AcidsEicosapentaenoic AcidIL1RN protein, humanIL6 protein, humanInterleukin 1 Receptor Antagonist ProteinInterleukin-6Leptin

Identifiers

PMID25802980
PMCPMC4581883
OpenAlexW1990532967

What OpenQuestion holds

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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.