Evidence map›Paper›PMID 37553799›Full record

ArticleAnnals of clinical and translational neurology2023

Vitamin D receptor and binding protein genes variants in patients with migraine.

Elena García-Martín, Santiago Navarro-Muñoz, Pedro Ayuso, Christopher Rodríguez, Mercedes Serrador, Hortensia Alonso-Navarro, Marisol Calleja, Silvina Espada-Rubio, Francisco Navacerrada, Laura Turpín-Fenoll and 7 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 31% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

17 authors at 3 institutions in 1 country.

Elena García-MartínUniversidad de Extremadura, University Institute of Molecular Pathology Biomarkers, Cáceres, Spain.ORCID 0000-0002-8094-046X
Santiago Navarro-MuñozSection of Neurology, Hospital La Mancha-Centro, Alcázar de San Juan, Spain.
Pedro AyusoUniversidad de Extremadura, University Institute of Molecular Pathology Biomarkers, Cáceres, Spain.
Christopher RodríguezUniversidad de Extremadura, University Institute of Molecular Pathology Biomarkers, Cáceres, Spain.
Mercedes SerradorDepartment of Family Medicine, Hospital "Príncipe de Asturias", Universidad de Alcalá, Alcalá de Henares, Madrid, Spain.
Hortensia Alonso-NavarroSection of Neurology, Hospital Universitario del Sureste, Madrid, Spain.ORCID 0000-0001-8644-2210
Marisol CallejaSection of Neurology, Hospital Universitario del Sureste, Madrid, Spain.
Silvina Espada-RubioSection of Neurology, Hospital Universitario del Sureste, Madrid, Spain.
Francisco NavacerradaSection of Neurology, Hospital Universitario del Sureste, Madrid, Spain.
Laura Turpín-FenollSection of Neurology, Hospital La Mancha-Centro, Alcázar de San Juan, Spain.
Marta Recio-BermejoSection of Neurology, Hospital La Mancha-Centro, Alcázar de San Juan, Spain.
Rafael García-RuizSection of Neurology, Hospital La Mancha-Centro, Alcázar de San Juan, Spain.
Jorge Millán-PascualSection of Neurology, Hospital La Mancha-Centro, Alcázar de San Juan, Spain.
José Francisco Plaza-NietoSection of Neurology, Hospital Universitario del Sureste, Madrid, Spain.
Esteban García-AlbeaDepartment of Medicine-Neurology, Universidad de Alcalá, Alcalá de Henares, Madrid, Spain.
José A G AgúndezUniversidad de Extremadura, University Institute of Molecular Pathology Biomarkers, Cáceres, Spain.ORCID 0000-0001-6895-9160
Félix Javier Jiménez-JiménezSection of Neurology, Hospital Universitario del Sureste, Madrid, Spain.ORCID 0000-0002-7558-7323
Hospital Universitario del Sureste · ESUniversidad de Extremadura · ESUniversidad de Alcalá · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesSeveral studies have shown a relationship between vitamin D and migraine, including the association between decreased serum 25-hydroxyvitamin D in patients with migraine and the positive effects of vitamin D supplementations in the therapy of this disease. Two single-nucleotide variants (SNVs) vitamin D receptor (VDR) gene, VDR rs2228570, and VDR rs731236 have shown an association with migraine risk in a previous case-control association study, while an exome sequencing study identified a rare variant in GC vitamin D binding protein gene. This study aims to look for the association between several common variants in these two genes and the risk for migraine.

methodsWe genotyped 290 patients diagnosed with migraine and 300 age-matched controls using specific TaqMan assays for VDR rs2228570, VDR rs731236, VDR rs7975232, VDR rs739837, VDR rs78783628, GC rs7041, and GC rs4588 SNVs.

resultsWe did not find an association between these SNVs and the risk for migraine. None of these SNVs were related to the positivity of a family history of migraine or with the presence of aura. The VDR rs731236A allele showed a significant association with the triggering of migraine attacks by ethanol (Pc = 0.007).

conclusionsIn summary, the results of the current study suggest a lack of association between common SNVs in the VDR and GC gene and the risk of developing migraine. The possible relationship between VDR rs731236 and the triggering of migraine episodes with ethanol deserves future studies.

Indexed as

Polymorphism, Single NucleotideReceptors, CalcitriolEthanolGenotypeHumansVitamin DEthanolReceptors, CalcitriolVitamin D

Identifiers

PMID37553799
PMCPMC10578880
OpenAlexW4385683993

What Socratic holds

Textmetadata
LicenceCC BY
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.