Evidence map›Paper›PMID 33762637›Full record

ArticleScientific reports2021

Common variants in KCNK5 and FHL5 genes contributed to the susceptibility of migraine without aura in Han Chinese population.

Zhao Jiang, Longrui Zhao, Xiaojie Zhang, Wenjuan Zhang, Yuxing Feng, Tao Li

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Genetics of migraine: where are we now?The journal of headache and pain · 2023
    Review
  3. Article
  4. 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 at 3 institutions in 1 country.

Zhao Jiang *Department of Forensic Medicine, School of Medicine and Forensics, Xi'an Jiaotong University Health Science Center, 76 Yanta West Road, Xi'an, 710061, Shaanxi, China.
Longrui Zhao *Department of Forensic Medicine, School of Medicine and Forensics, Xi'an Jiaotong University Health Science Center, 76 Yanta West Road, Xi'an, 710061, Shaanxi, China.
Xiaojie ZhangDepartment of Neurology, Xianyang Hospital of Yan'an University, Xi'an, Shaanxi, China.
Wenjuan ZhangDepartment of Neurology, Xijing Hospital of Air Force Medical University, Xi'an, Shaanxi, China.
Yuxing FengDepartment of Rehabilation and Pain Medicine, the Ninth People's Hospital of Chongqing, Chongqing, China.
Tao LiDepartment of Forensic Medicine, School of Medicine and Forensics, Xi'an Jiaotong University Health Science Center, 76 Yanta West Road, Xi'an, 710061, Shaanxi, China. litao050428@mail.xjtu.edu.cn.
Xi'an Jiaotong University · CNXijing Hospital · CNYan'an University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recent genome-wide meta study suggested that rs67338227 in the FHL5 gene and rs10456100 in the KCNK5 gene are associated with migraine from 27 population-based cohorts excluding Chinese population. Given that migraine without aura (MO) is the most common subtype of migraine, our aim was to systematically investigate the relationship of common variants in FHL5 and KCNK5 genes with the susceptibility to MO and provide clues as to the nature of the mechanisms involved in the etiology of migraine. A total of 3306 subjects including 1042 patients with MO and 2264 controls were recruited for the discovery stage, and 2530 individuals including 842 patients with MO and 1688 controls for the replication stage. Twenty-two tag SNPs (7 from FHL5 and 15 from KCNK5) were selected for genotyping. Genetic associations were analyzed at both single-marker and haplotype levels. Potential functional consequences of the significant SNPs were analyzed using gene expression data obtained from the GTEx database. Two SNPs, rs10456100 (KCNK5, P = 9.01 × 10

Indexed as

AdultAsian PeopleCase-Control StudiesChinaFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansLIM Domain ProteinsLinkage DisequilibriumMaleMiddle AgedMigraine without AuraPolymorphism, Single NucleotidePotassium Channels, Tandem Pore DomainFHL5 protein, humanKCNK5 protein, humanLIM Domain ProteinsPotassium Channels, Tandem Pore DomainTranscription Factors

Identifiers

PMID33762637
PMCPMC7990926
OpenAlexW3136873721

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.