Evidence map›Paper›PMID 39333847›Full record

ArticleThe journal of headache and pain2024

Improved polygenic risk prediction in migraine-first patients.

Dora Torok, Peter Petschner, Daniel Baksa, Gabriella Juhasz

Abstract read
In one paragraph

Article in The journal of headache and pain, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. What does a migraine aura look like?-A systematic review.The journal of headache and pain · 2025
    Pooled it
  2. Article
  3. Article
  4. The interictal transcriptomic map of migraine without aura.The journal of headache and pain · 2025
    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

4 authors.

Dora Torok *Department of Pharmacodynamics, Faculty of Pharmaceutical Sciences, Semmelweis University, Nagyvarad ter 4., Budapest, 1096, Hungary.
Peter Petschner *Department of Pharmacodynamics, Faculty of Pharmaceutical Sciences, Semmelweis University, Nagyvarad ter 4., Budapest, 1096, Hungary.
Daniel BaksaDepartment of Pharmacodynamics, Faculty of Pharmaceutical Sciences, Semmelweis University, Nagyvarad ter 4., Budapest, 1096, Hungary.
Gabriella JuhaszDepartment of Pharmacodynamics, Faculty of Pharmaceutical Sciences, Semmelweis University, Nagyvarad ter 4., Budapest, 1096, Hungary. juhasz.gabriella@semmelweis.hu.

Funding

New National Excellence Program ÚNKP-23-4-II-SE-2Postdoctoral Fellowships for Research in Japan, standard program P20809
6 · The paper itself

Abstract

backgroundRecent meta-analyses estimated 14.6% and 11.2% SNP-based heritability of migraine, compared to twin-heritability estimates of 30-60%. This study aimed to investigate heritability estimates in "migraine-first" individuals, patients for whom G43 (migraine with or without aura) was their first medical diagnosis in their lifetime.

findingsUsing data from the UK Biobank (N = 199,929), genome-wide association studies (GWAS) were conducted on 6,139 migraine-first patients and 193,790 healthy controls. SNP-based heritability was estimated using SumHer, yielding 19.37% (± 0.019) for all SNPs and 21.31% (± 0.019) for HapMap3 variants, substantially surpassing previous estimates. Key risk loci included PRDM16, FHL5, ASTN2, STAT6/LRP1, and SLC24A3, and pathway analyses highlighted retinol metabolism and steroid hormone biosynthesis as important pathways in these patients.

conclusionsThe findings underscore that excluding comorbidities at onset time can enhance heritability estimates and genetic signal detection, significantly reducing the extent of "missing heritability" in migraine.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyMultifactorial InheritancePolymorphism, Single NucleotideAdultDNA-Binding ProteinsFemaleHumansLow Density Lipoprotein Receptor-Related Protein-1MaleMiddle AgedMigraine DisordersMigraine with AuraMigraine without AuraTranscription FactorsUnited KingdomDNA-Binding ProteinsLow Density Lipoprotein Receptor-Related Protein-1LRP1 protein, humanPRDM16 protein, humanTranscription FactorsDisease onsetGeneticsMigraineMissing heritability

Identifiers

PMID39333847
PMCPMC11438044

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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.