Evidence map›Paper›PMID 28360598›Full record

ArticleNoro psikiyatri arsivi2014

Genetic Susceptibility to Multiple Sclerosis: The Role of FOXP3 Gene Polymorphism.

Nihal Işik, Nüket Yildiz Manukyan, İlknur Aydin Cantürk, Fatma Candan, Ayşen Ünsal Çakmak, Güher Saru Han Direskeneli

Open access · greenAbstract read
In one paragraph

Article in Noro psikiyatri arsivi, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 77% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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.

Nihal IşikClinic of Neurology, Medeniyet University Göztepe Training and Research Hospital, İstanbul, Turkey.
Nüket Yildiz ManukyanClinic of Neurology, Ministry Health Fatih Sultan Mehmet Training and Research Hospital, İstanbul, Turkey.
İlknur Aydin CantürkClinic of Neurology, Medeniyet University Göztepe Training and Research Hospital, İstanbul, Turkey.
Fatma CandanClinic of Neurology, Medeniyet University Göztepe Training and Research Hospital, İstanbul, Turkey.
Ayşen Ünsal ÇakmakClinic of Neurology, Medeniyet University Göztepe Training and Research Hospital, İstanbul, Turkey.
Güher Saru Han DireskeneliDepartment of Neurology, İstanbul University İstanbul Faculty of Medicine, İstanbul, Turkey.
Istanbul Medeniyet University · TRFatih Sultan Mehmet Eğitim Ve Araştırma Hastanesi · TRIstanbul University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIt is well recognized that both genetic and environmental factors play an important role in the pathogenesis of multiple sclerosis (MS). Immune pathogenesis of MS focuses on pathogenic CD4+ T lymphocytes. CD4+CD25+ regulatory T cells have suppressive function in this cell group. FOXP3 (forkhead boxP3) transcription factor is a key structure in the development and function of regulatory cells. Functional alterations in FOXP3 gene expression have been observed in various autoimmune diseases.

methodsWe screened a non-synonymous coding single nucleotide polymorphism (exon +2710 C/T) (rs2232369) of human FOXP3 gene in 148 MS patients (118 with Relapsing Remitting MS, 30 with Secondary Progressive MS) and 102 age- and sex-matched healthy controls. The association of polymorphisms with susceptibility, and course of the disease was evaluated.

resultsWe could not detect any single nucleotide polymorphism in MS patients, however, polymorphic allele was detected in 3% of the control group. Consequently, a genetic association between the FOXP3 gene polymorphism and MS was not revealed.

conclusionThe distribution of this polymorphism has not been screened in any other MS populations before. Although we could not succeed to find any association between susceptibility to MS and screened FOXP3 gene polymorphisms, we suggest that this particular polymorphism is not appropriate for these kind of studies in the future.

Indexed as

FOXP3genotypeMultiple Sclerosispolymorphism

Identifiers

PMID28360598
PMCPMC5370262
OpenAlexW2333981978

What OpenQuestion holds

Textmetadata
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.