Evidence map›Paper›PMID 42796966›Full record

Trial reportNutrients2026

Omega-3 Supplementation Modulates Whole-Blood EPA and DHA Without Improving Patient-Reported Outcomes in Youth with Migraine: A Quasi-Randomized Pilot Trial.

Samantha Glover, Anne E Sanders, Daisy Zamora, Keturah R Faurot, Saame Raza Shaikh, Kimon Divaris, Klaus Werner, Steven P Trau, Jaclyn Bain, Jialiu Xie and 5 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Nutrients, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Samantha GloverDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0009-0002-7049-3405
Anne E SandersDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0003-2607-9514
Daisy ZamoraDepartment of Physical Medicine and Rehabilitation, School of Medicine, University of North Carolina, Chapel Hill, NC 27514, USA.ORCID 0000-0003-2114-5156
Keturah R FaurotDepartment of Physical Medicine and Rehabilitation, School of Medicine, University of North Carolina, Chapel Hill, NC 27514, USA.ORCID 0000-0001-6122-7821
Saame Raza ShaikhDepartment of Nutrition, Gillings School of Global Public Health and School of Medicine, University of North Carolina, Chapel Hill, NC 27599, USA.
Kimon DivarisDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0003-1290-7251
Klaus WernerDivision of Pediatric Neurology, Duke University Medical Center, Durham, NC 27705, USA.
Steven P TrauDepartment of Neurology, School of Medicine, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0002-1068-9951
Jaclyn BainDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0009-0000-9405-703X
Jialiu XieDepartment of Biostatistics, Gillings School of Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0002-0560-7982
Sydney DanzeDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.
Sajan SinghDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.
Thomas SouthernDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0009-0006-5890-2527
Joseph IskanderDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.
Caroline M SawickiDepartment of Pediatric Dentistry and Dental Public Health, Adams School of Dentistry, University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0001-9295-9849

Funding

North Carolina Translational and Clinical Sciences Institute (NC TraCS)UM1TR004406 · NCATS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NICHOLAS J SHAHEEN · 2023 to 2026
$37.5M
UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Venkata Saroja Voruganti · 1999 to 2026
$31.6M
NCATS NIH HHS UM1 TR004406NIDDK NIH HHS P30 DK056350NIDDK NIH HHS P30DK056350
6 · The paper itself

Abstract

BACKGROUND/

objectivesOmega-3 polyunsaturated fatty acids (PUFAs) influence lipid-mediated inflammatory pathways implicated in migraine, yet randomized trial data evaluating biologic effects of omega-3 supplementation in youth with migraine remain limited. This pilot quasi-randomized clinical trial aimed to determine whether 12 weeks of omega-3 PUFA supplementation produces measurable changes in whole-blood EPA and DHA levels in children and adolescents with migraine, and to characterize changes in patient-reported measures of pain, migraine-related disability, and psychological distress.

methodsWe conducted a parallel-group, quasi-randomized, double-blind, placebo-controlled trial in children and adolescents (ages 10-17) with migraine diagnosed per International Classification of Headache Disorders, 3rd edition criteria, recruited from pediatric neurology clinics at two academic medical centers. Of 57 participants allocated 1:1 to daily omega-3 PUFA supplementation (340 mg EPA + 510 mg DHA) or coconut oil placebo for 12 weeks, 44 completed the study and were analyzed. The primary outcome was change in whole-blood omega-3 PUFA index. Secondary outcomes included patient-reported measures of pain intensity, pain interference, migraine-related disability, and psychological distress. Exploratory outcomes included changes in omega-6/omega-3 and arachidonic acid/eicosapentaenoic acid (AA/EPA) ratios. Between-group differences were evaluated using ANCOVA adjusting for baseline values.

resultsOmega-3 supplementation significantly altered lipid biomarker profiles. Compared with placebo, the intervention group demonstrated greater increases in omega-3 PUFA index (adjusted mean difference 1.64; 95% CI 0.94-2.35;

conclusionsOmega-3 PUFA supplementation significantly altered lipid biomarker profiles in youth with migraine over 12 weeks, supporting a measurable whole-blood EPA + DHA response in this proof-of-concept trial. Future larger-scale trials with longer duration are needed to evaluate clinical effects.

Indexed as

Dietary SupplementsDocosahexaenoic AcidsEicosapentaenoic AcidFatty Acids, Omega-3Migraine DisordersPatient Reported Outcome MeasuresAdolescentChildDouble-Blind MethodFemaleHumansMalePilot ProjectsTreatment OutcomeDocosahexaenoic AcidsEicosapentaenoic AcidFatty Acids, Omega-3dietary supplementationlipid biomarkersomega-3 fatty acidspediatric migraine

Identifiers

PMID42796966
PMCPMC13610828

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.