Evidence map›Paper›PMID 39186221›Full record

ArticleJournal of endocrinological investigation2025

Effect of docosahexaenoic acid as an anti-inflammatory for Caco-2 cells and modulating agent for gut microbiota in children with obesity (the DAMOCLE study).

C Lammi, E Ottaviano, G Fiore, C Bollati, L d'Adduzio, M Fanzaga, C Ceccarani, S Vizzuso, G Zuccotti, E Borghi and 1 more

Abstract read
In one paragraph

Article in Journal of endocrinological investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
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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

11 authors.

C LammiDepartment of Pharmaceutical Sciences, University of Milan, 20133, Milan, Italy.
E OttavianoDepartment of Health Sciences, University of Milan, 20142, Milan, Italy.
G FioreDepartment of Health Sciences, University of Milan, 20142, Milan, Italy. giulia.fiore@unimi.it.ORCID http://orcid.org/0000-0002-6100-5687
C BollatiDepartment of Pharmaceutical Sciences, University of Milan, 20133, Milan, Italy.
L d'AdduzioDepartment of Pharmaceutical Sciences, University of Milan, 20133, Milan, Italy.
M FanzagaDepartment of Pharmaceutical Sciences, University of Milan, 20133, Milan, Italy.
C CeccaraniInstitute for Biomedical Technologies, CNR, Segrate, Italy.
S VizzusoDepartment of Pediatrics, Vittore Buzzi Children's Hospital, University of Milan, Via Lodovico Castelvetro 32, 20154, Milan, Italy.
G ZuccottiDepartment of Pediatrics, Vittore Buzzi Children's Hospital, University of Milan, Via Lodovico Castelvetro 32, 20154, Milan, Italy.
E BorghiDepartment of Health Sciences, University of Milan, 20142, Milan, Italy.
E VerduciDepartment of Health Sciences, University of Milan, 20142, Milan, Italy.

Funding

NextGenerationEU D93C22000890001
6 · The paper itself

Abstract

purposeDocosahexaenoic acid (DHA) is a long-chain omega-3 polyunsaturated fatty acid. We investigated the dual health ability of DHA to modulate gut microbiota in children with obesity and to exert anti-inflammatory activity on human intestinal Caco-2 cells.

methodsIn a pilot study involving 18 obese children (8-14 years), participants received a daily DHA supplement (500 mg/day) and dietary intervention from baseline (T0) to 4 months (T1), followed by dietary intervention alone from 4 months (T1) to 8 months (T2). Fecal samples, anthropometry, biochemicals and dietary assessment were collected at each timepoint. At preclinical level, we evaluated DHA's antioxidant and anti-inflammatory effects on Caco-2 cells stimulated with Hydrogen peroxide (H

resultsTen children were included in final analysis. No major changes were observed for anthropometric and biochemical parameters, and participants showed a low dietary compliance at T1 and T2. DHA supplementation restored the Firmicutes/Bacteroidetes ratio that was conserved also after the DHA discontinuation at T2. DHA supplementation drove a depletion in Ruminococcaceae and Dialisteraceae, and enrichment in Bacteroidaceae, Oscillospiraceae, and Akkermansiaceae. At genus level, Allisonella was the most decreased by DHA supplementation. In Caco-2 cells, DHA decreased H

conclusionAn improvement in gut dysbiosis of children with obesity seems to be triggered by DHA and to continue after discontinuation. The ability to modulate gut microbiota, matches also with an anti-inflammatory effect of DHA on Caco-2 cells.

Indexed as

Anti-Inflammatory AgentsDocosahexaenoic AcidsGastrointestinal MicrobiomePediatric ObesityAdolescentCaco-2 CellsChildDietary SupplementsFemaleHumansMalePilot ProjectsAnti-Inflammatory AgentsDocosahexaenoic AcidsAnti-inflammatory activityAntioxidant effectCaco-2 cellsChildhood obesityDocosahexaenoic acidGut microbiota

Identifiers

PMID39186221
PMCPMC11785711

What Socratic 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 Socratic graph.