Evidence map›Paper›PMID 41935312›Full record

SynthesisThe journal of headache and pain2026

Migraine in pediatric population: the role of biochemical markers.

Gabriele Monte, Carmen Granata, Fabiana Ursitti, Giorgia Sforza, Massimiliano Valeriani, Laura Papetti

Abstract readSystematic Review
In one paragraph

Synthesis in The journal of headache and pain, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

Gabriele MonteDevelopmental Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Piazza di Sant'Onofrio 4, 00165, Rome, Italy. gabriele.monte@opbg.net.
Carmen GranataChild Neurology and Psychiatry Unit, Systems Medicine Department, Tor Vergata University of Rome, Rome, Italy.
Fabiana UrsittiDevelopmental Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Piazza di Sant'Onofrio 4, 00165, Rome, Italy.
Giorgia SforzaDevelopmental Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Piazza di Sant'Onofrio 4, 00165, Rome, Italy.
Massimiliano ValerianiDevelopmental Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Piazza di Sant'Onofrio 4, 00165, Rome, Italy.
Laura PapettiDevelopmental Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Piazza di Sant'Onofrio 4, 00165, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiagnosis of migraine remains primarily clinical, and objective biological markers are lacking. Although biomarker research has expanded considerably in adults, evidence in pediatric populations remains fragmented and heterogeneous. This systematic review aimed to synthesize current data on biochemical markers in pediatric migraine and to evaluate their potential diagnostic, monitoring, prognostic, and treatment-response roles.

methodsThe review was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. PubMed, Embase and Scopus were searched up to January 1st, 2026. Studies investigating biochemical markers in individuals younger than 18 years diagnosed with episodic or chronic migraine according to International Classification of Headache Disorders 3rd edition (ICHD-3) criteria were included. Biomarkers assessed in blood, saliva, urine, cerebrospinal fluid, or stool were considered. Due to substantial heterogeneity in study design, sampling timing and laboratory methods, findings were synthesized narratively.

resultsTwenty-eight studies met inclusion criteria. Neuropeptides were the most extensively investigated biomarkers. Ictal elevation of calcitonin gene-related peptide (CGRP) was the most reproducible finding, supporting a disease-activity monitoring role, whereas interictal levels showed inconsistent results. Pituitary adenylate cyclase–activating polypeptide 38 (PACAP-38) and vasoactive intestinal peptide (VIP) demonstrated variable associations and may contribute within multimarker panels. Mitochondrial stress markers (growth differentiation factor-15, fibroblast growth factor-21 and hypoxia-inducible factor-1α) were elevated during attacks and in chronic migraine, suggesting links with metabolic stress and disease burden. MicroRNAs emerged as preliminary treatment-responsive candidates. Gut microbiota studies showed consistent β-diversity alterations and shifts in tryptophan metabolism; ratio-based kynurenine metabolites displayed promising diagnostic performance. Among inflammatory markers, tumor necrosis factor (TNF)-axis activation and interleukin (IL)-12p70 were the most reproducible signals.

conclusionsNo single biomarker currently supports standalone clinical application. Pathway-based multimarker approaches may improve biological stratification and monitoring in pediatric migraine. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

BiomarkersMigraine DisordersChildHumansBiomarkersBiomarkersCGRPChildrenCytokinesMicrobiotaMigraineMitochondrial dysfunction

Identifiers

PMID41935312
PMCPMC13059414

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.