Evidence map›Paper›PMID 35332405›Full record

ArticleClinical rheumatology2022

Association of a miRNA-binding site polymorphism in IL-16 gene with disease risk and clinical characteristics of rheumatoid arthritis and systemic lupus erythematosus.

Somayeh Zeinalzadeh, Nahid Kheradmand, Ghazal Rasouli, Emran Esmaeilzadeh, Bahram Pakzad, Javad Behroozi, Mohsen Chamanara, Mojtaba Yousefi Zoshk, Naeim Ehtesham, Mehrdad Nasrollahzadeh Sabet

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Article in Clinical rheumatology, 2022. 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
0.9field-weighted citation impact, top 28% 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, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Polymorphisms in microRNA binding site ofExperimental and therapeutic medicine · 2023
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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

10 authors at 4 institutions in 1 country.

Somayeh ZeinalzadehFetal Health Research Center, Hope Generation Foundation, Tehran, Iran.
Nahid KheradmandDepartment of Medical Genetics and Molecular Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Ghazal RasouliFaculty of Basic Sciences, Central Tehran Branch, Islamic Azad University, Isfahan, Iran.
Emran EsmaeilzadehFetal Health Research Center, Hope Generation Foundation, Tehran, Iran.
Bahram PakzadDivision of Rheumatology, Department of Internal Medicine, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran.
Javad BehrooziResearch Center for Cancer Screening and Epidemiology, AJA University of Medical Sciences, Tehran, Iran.
Mohsen ChamanaraToxicology Research Center, Aja University of Medical Sciences, Tehran, Iran.
Mojtaba Yousefi ZoshkTrauma Research Center, Aja University of Medical Sciences, Tehran, Iran.
Naeim EhteshamFetal Health Research Center, Hope Generation Foundation, Tehran, Iran.
Mehrdad Nasrollahzadeh SabetSchool of Medicine, Aja University of Medical Science, Tehran, Iran. M.nasrollahzadehs@yahoo.com.ORCID http://orcid.org/0000-0003-3402-4628
Aja University of Medical Sciences · IRIslamic Azad University, Isfahan · IRMashhad University of Medical Sciences · IRUniversity of Isfahan · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introduction/objectives. Single nucleotide polymorphisms (SNPs) located at the 3'-UTR region of the target genes of microRNAs (miRNAs) can dysregulate their expression via disrupting the binding site of miRNAs. Interleukin-16 (IL-16) is involved in the pathogenesis of rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE). In the current study, we assessed the possible association between rs1131445 polymorphism in IL-16 gene with risk and clinical characteristics of RA and SLE in the Iranian population.

methodsIn this case-control study, 120 patients with RA, 120 patients with SLE, and 120 unrelated healthy subjects were collected to estimate rs1131445 (T > C) polymorphism in IL-16 gene using real-time PCR high-resolution melting (HRM) method.

resultsOur results demonstrated considerable associations between TC genotype and C allele of rs1131445 with enhanced risk of RA (OR

conclusionThese results proposed a significant association between IL-16 polymorphism and augmented risk of RA and clinical characteristics of RA and SLE.

Indexed as

Arthritis, RheumatoidInterleukin-16Lupus Erythematosus, SystemicMicroRNAsBinding SitesCase-Control StudiesGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansIranPolymorphism, Single NucleotideIl16 protein, humanInterleukin-16MicroRNAsIL-16MicroRNAsRheumatoid arthritisSingle nucleotide polymorphismSystemic lupus erythematosus

Identifiers

PMID35332405
OpenAlexW4220733734

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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.