Evidence map›Paper›PMID 31438837›Full record

ArticleBMC immunology2019

Genetic polymorphisms and epigenetic regulation of survivin encoding gene, BIRC5, in multiple sclerosis patients.

Dariush Rahban, Forogh Mohammadi, Mehdi Alidadi, Taha Ghantabpour, Pedram Abbasi Ghasem Kheyli, Majid Ahmadi

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

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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

6 authors at 4 institutions in 1 country.

Dariush RahbanDepartment of Nanomedicine, School of Advanced Medical Technologies, Tehran University of Medical Sciences, Tehran, Iran. rahbandariush@gmail.com.
Forogh MohammadiAgriculture faculty, Department of Veterinary, Kermanshah Branch, Islamic Azad University, Kermanshah, Iran.
Mehdi AlidadiDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Taha GhantabpourDepartment of Anatomy, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Pedram Abbasi Ghasem KheyliParamedical Department, Shiraz University of Medical Sciences, Shiraz, Iran.
Majid AhmadiStem Cell Research Center, Tabriz University of Medical Sciences, Daneshghah St., Imam Reza Hospital, Tabriz, Iran. ahmadi.m@tbzmed.ac.ir.
Tehran University of Medical Sciences · IRImam Reza Hospital · IRIslamic Azad University of Kermanshah · IRShiraz University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe persistent the inflammatory condition in multiple sclerosis (MS) may due to the aberrant regulation of the elimination of the pathogenic autoreactive lymphocytes through apoptosis. Survivin, encoded by the BIRC5 gene, has been indicated to be involved in the regulation of apoptosis. This survey intended to investigate the genetic and microRNA mediated regulation of survivin in relapsing-remitting MS (RRMS) disease.

resultsIt was observed that the C allele (OR = 1.38, 95% CI = 1.05-1.348, P = 0.022) and CC genotype (OR = 1.84, 95% CI = 1.06-3.19; P = 0.029) in the rs9904341 polymorphism increased the disease risk. Furthermore, miR-34a was significantly downregulated (Fold change = 0.41, P = 0.001) in the PBMCs from RRMS subjects. Survivin mRNA expression in PBMCs and serum survivin level were increased in RRMS patients in comparison to the controls. Downregulation of miR-34a was negatively correlated with increased survivin level.

conclusionAlthough the genetic polymorphism of BIRC5 gene was associated with the disease risk, miR-34a was suggested to be involved in the regulation of survivin in the RRMS patients.

Indexed as

Epigenesis, GeneticGenetic Predisposition to DiseasePolymorphism, Single NucleotideAdultAllelesApoptosisBiomarkersCase-Control StudiesFemaleGenotypeHumansLeukocytes, MononuclearMaleMicroRNAsMiddle AgedMultiple SclerosisBiomarkersBIRC5 protein, humanMicroRNAsSurvivinApoptosisBIRC5 genemicroRNAMultiple sclerosisSurvivin

Identifiers

PMID31438837
PMCPMC6704704
OpenAlexW2969532133

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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.