Evidence map›Paper›PMID 39513898›Full record

ReviewCells2024

Omega-3 Fatty Acids and Neuroinflammation in Depression: Targeting Damage-Associated Molecular Patterns and Neural Biomarkers.

Ikbal Andrian Malau, Jane Pei-Chen Chang, Yi-Wen Lin, Cheng-Chen Chang, Wei-Che Chiu, Kuan-Pin Su

Abstract readReview
In one paragraph

Review in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
–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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Review
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  5. Article
  6. Evaluating the causal effects of circulating metabolites on major depression disorder.European archives of psychiatry and clinical neuroscience · 2026
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  8. Krenning score enhances integrated biomarker models for survival prediction in PRRT-treated GEP-NET: a retrospective cohort study.Cancer imaging : the official publication of the International Cancer Imaging Society · 2026
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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.

Ikbal Andrian MalauMind-Body Interface Research Center (MBI-Lab), China Medical University Hospital, Taichung 404, Taiwan.ORCID 0000-0002-6716-4830
Jane Pei-Chen ChangMind-Body Interface Research Center (MBI-Lab), China Medical University Hospital, Taichung 404, Taiwan.ORCID 0000-0001-5582-0928
Yi-Wen LinGraduate Institute of Acupuncture Science and Chinese Medicine Research Center, College of Medicine, China Medical University, Taichung 404, Taiwan.
Cheng-Chen ChangDepartment of Psychiatry, Chung Shan Medical University Hospital, Taichung 402, Taiwan.ORCID 0000-0002-9491-6866
Wei-Che ChiuDepartment of Psychiatry, Cathay General Hospital, Taipei 106, Taiwan.ORCID 0000-0001-8549-1432
Kuan-Pin SuMind-Body Interface Research Center (MBI-Lab), China Medical University Hospital, Taichung 404, Taiwan.ORCID 0000-0002-4501-2502

Funding

An-Nan Hospital, China Medical University, Tainan, Taiwan ANHRF 110-13An-Nan Hospital, China Medical University, Tainan, Taiwan ANHRF 111-52An-Nan Hospital, China Medical University, Tainan, Taiwan ANHRF 112-24An-Nan Hospital, China Medical University, Tainan, Taiwan ANHRF 112-47An-Nan Hospital, China Medical University, Tainan, Taiwan ANHRF 113-24An-Nan Hospital, China Medical University, Tainan, Taiwan ANHRF 113-38An-Nan Hospital, China Medical University, Tainan, Taiwan ANHRF 113-40Higher Education Sprout Project by the Ministry of Education (MOE), Taiwan CMRC-CMA-2the China Medical University Hospital, Taichung, Taiwan 111-245the China Medical University Hospital, Taichung, Taiwan 112-086the China Medical University Hospital, Taichung, Taiwan 112-097the China Medical University Hospital, Taichung, Taiwan 112-109the China Medical University Hospital, Taichung, Taiwan 112-232the China Medical University Hospital, Taichung, Taiwan DMR-110-124the China Medical University Hospital, Taichung, Taiwan DMR-HHC-109-11the China Medical University Hospital, Taichung, Taiwan HHC-109-12the China Medical University Hospital, Taichung, Taiwan HHC-110-10the China Medical University Hospital, Taichung, Taiwan HHC-111-8the China Medical University, Taichung, Taiwan CMU 110-AWARD-02the China Medical University, Taichung, Taiwan CMU 110-N-17the China Medical University, Taichung, Taiwan CMU 111-SR-73the National Science and Technology Council (NSTC), Taiwan 110-2314-B-039-029-MY3the National Science and Technology Council (NSTC), Taiwan 110-2320-B-039-047-MY3the National Science and Technology Council (NSTC), Taiwan 110-2813-C-039-327-Bthe National Science and Technology Council (NSTC), Taiwan 111-2314-B-039-041-MY3the National Science and Technology Council (NSTC), Taiwan 111-2321-B-006-008the National Science and Technology Council (NSTC), Taiwan 113-2314-B-039-046the National Science and Technology Council (NSTC), Taiwan 113-2923-B-039-001-MY3the National Science and Technology Council (NSTC), Taiwan NSTC 109-2320-B-038-057-MY3the National Science and Technology Council (NSTC), Taiwan NSTC 110-2320-B-039-048-MY2the National Science and Technology Council (NSTC), Taiwan NSTC 110-2321-B-006-004the National Science and Technology Council (NSTC), Taiwan NSTC 110-2811-B-039-507
6 · The paper itself

Abstract

Major Depressive Disorder (MDD) is a prevalent mental health condition with a complex pathophysiology involving neuroinflammation, neurodegeneration, and disruptions in neuronal and glial cell function. Microglia, the innate immune cells of the central nervous system, release inflammatory cytokines in response to pathological changes associated with MDD. Damage-associated molecular patterns (DAMPs) act as alarms, triggering microglial activation and subsequent inflammatory cytokine release. This review examines the cellular mechanisms underlying MDD pathophysiology, focusing on the lipid-mediated modulation of neuroinflammation. We explore the intricate roles of microglia and astrocytes in propagating inflammatory cascades and discuss how these processes affect neuronal integrity at the cellular level. Central to our analysis are three key molecules: High Mobility Group Box 1 (HMGB1) and S100 Calcium Binding Protein β (S100β) as alarmins, and Neuron-Specific Enolase (NSE) as an indicator of neuronal stress. We present evidence from in vitro and ex vivo studies demonstrating how these molecules reflect and contribute to the neuroinflammatory milieu characteristic of MDD. The review then explores the potential of omega-3 polyunsaturated fatty acids (ω-3 PUFAs) as neuroinflammation modulators, examining their effects on microglial activation, cytokine production, and neuronal resilience in cellular models of depression. We critically analyze experimental data on how ω-3 PUFA supplementation influences the expression and release of HMGB1, S100β, and NSE in neuronal and glial cultures. By integrating findings from lipidomic and cellular neurobiology, this review aims to elucidate the mechanisms by which ω-3 PUFAs may exert their antidepressant effects through modulation of neuroinflammatory markers. These insights contribute to our understanding of lipid-mediated neuroprotection in MDD and may inform the development of targeted, lipid-based therapies for both depression and neurodegenerative disorders.

Indexed as

BiomarkersFatty Acids, Omega-3Neuroinflammatory DiseasesAlarminsAnimalsDepressionHMGB1 ProteinHumansInflammationMajor Depressive DisorderMicrogliaNeuronsAlarminsBiomarkersFatty Acids, Omega-3HMGB1 ProteinDAMPsdepressionHMGB1NSEomega-3 polyunsaturated fatty acidsS100β

Identifiers

PMID39513898
PMCPMC11544853

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.