Evidence map›Paper›PMID 37085790›Full record

SynthesisBMC neurology2023

Enlightening the association between TNF-α -308 G > A and migraine: a meta-analysis with meta-regression and trial sequential analysis.

Amrit Sudershan, Srishty Sudershan, Mohd Younis, Meenakshi Bhagat, Agar Chander Pushap, Hardeep Kumar, Parvinder Kumar

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in BMC neurology, 2023. 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
2.0field-weighted citation impact, top 14% 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, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Role of TNFPain research & management · 2024
    Review
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

7 authors at 4 institutions in 1 country.

Amrit SudershanInstitute of Human Genetics, University of Jammu, Jammu & Kashmir, Jammu, India, 180006.
Srishty SudershanDepartment of Zoology, University of Jammu, Jammu and Kashmir, Jammu, India, 180006.
Mohd YounisInstitute of Human Genetics, University of Jammu, Jammu & Kashmir, Jammu, India, 180006.
Meenakshi BhagatDepartment of Zoology, University of Jammu, Jammu and Kashmir, Jammu, India, 180006.
Agar Chander PushapDepartment of Education, Dakshina Bharat Hindi Prachar Sabha, Madras, India, 600017.
Hardeep KumarDepartment of Neurology, Super Specialty Hospital, Jammu and Kashmir, Jammu, India, 180006.
Parvinder KumarInstitute of Human Genetics, University of Jammu, Jammu & Kashmir, Jammu, India, 180006. Parvinderkb2003@gmail.com.
University of Jammu · INDakshina Bharat Hindi Prachar Sabha · INJammu Hospital · INUniversity of Kashmir · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMigraine is a complex neurological disorder that is characterized by a "lower threshold of neuronal hyperexcitability" with distinctive periodicity and complex vascular dysfunction. Genetic factors have impacted incredibly on the susceptibility of migraine and one such example is the TNF-α 308G > A.

aimTherefore, we aim to provide a glimpse of the association of the TNF-α 308G > A risk on the susceptibility of migraine.

methodThe pooled odds ratio with the associated 95% of confidence interval were calculated using different genetic models. Heterogeneity was accessed by using Cochran's Q Test and I

resultA total of 13 studies with cases: 7193 and controls: 23,091 were included and after using different genetic models, no overall association with migraine and its clinical subtype migraine with aura was observed (Allele model "OR: 1.28, 95% C.I. [0.96-1.69] and OR: 0.99,95% C.I. [0.69-1.42]) respectively. Interestingly, after sub-grouping using the "ethnicity criteria" in the migraine group, it was observed that the allelic genetic model and the dominant model were found to be significantly associated with the Asian ethnic group (OR: 1.79, 95% C.I. [1.13-2.84], and OR: 1.85, 95% C.I. [1.0927; 3.1580].

conclusionIn conclusion, the present meta-analysis has provided evidence that 308G > A increases the risk of migraine only in the Asian population.

Indexed as

Asian PeopleGenetic Predisposition to DiseaseMigraine DisordersTumor Necrosis Factor-alphaAsianHumansPolymorphism, Single NucleotideTNF protein, humanTumor Necrosis Factor-alpha-308 g > aMigrainers1800629TNF-α

Identifiers

PMID37085790
PMCPMC10120225
OpenAlexW4366742725

What OpenQuestion 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 OpenQuestion graph.