Evidence map›Paper›PMID 34036107›Full record

Observational studyJournal of immunology research2021

miR-183-5p Is a Potential Molecular Marker of Systemic Lupus Erythematosus.

Shaolan Zhou, Jing Zhang, Pengfei Luan, Zhanbing Ma, Jie Dang, Hong Zhu, Qian Ma, Yanfeng Wang, Zhenghao Huo

Erratum issuedOpen access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of immunology research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Shaolan ZhouDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0002-0915-3818
Jing ZhangDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.
Pengfei LuanDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0003-0831-5587
Zhanbing MaDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0002-8392-3008
Jie DangDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0001-9138-3083
Hong ZhuDepartment of Rheumatology, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0003-3999-9408
Qian MaDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0002-3272-9723
Yanfeng WangDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0002-2318-3132
Zhenghao HuoDepartment of Medical Genetics and Cell Biology, College of Basic Medicine, Ningxia Medical University, Yinchuan, Ningxia, China.ORCID https://orcid.org/0000-0003-3625-2931
Ningxia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate microRNA (miRNA) expression profiles in individuals with systemic lupus erythematosus (SLE) and identify the valuable miRNA biomarkers in diagnosing and monitoring SLE.

methodsNext-generation sequencing (NGS) was performed to assess miRNA amounts in peripheral blood mononuclear cells (PBMCs) from four SLE cases and four healthy controls. Quantitative polymerase chain reaction (qPCR) was carried out for validating candidate miRNAs in 32 SLE cases and 32 healthy controls. In addition, receiver operating characteristic (ROC) curve analysis was completed to evaluate diagnostic performance. Finally, the associations of candidate miRNAs with various characteristics of SLE were analyzed.

resultsA total of 157 miRNAs were upregulated, and 110 miRNAs were downregulated in PBMCs from SLE cases in comparison to healthy controls, of which the increase of miR-183-5p and decrease of miR-374b-3p were validated by qPCR and both showed good diagnostic performance for SLE diagnosis. Besides, miR-183-5p expression levels displayed a positive association with SLE disease activity index (SLEDAI) and anti-dsDNA antibody amounts.

conclusionOur data indicated that miR-183-5p is a promising biomarker of SLE.

Indexed as

AdultAntibodies, AntinuclearBiomarkersCase-Control StudiesFemaleGene Expression ProfilingHealthy VolunteersHumansLeukocytes, MononuclearLupus Erythematosus, SystemicMaleMicroRNAsROC CurveUp-RegulationYoung AdultAntibodies, Antinuclearanti-dsDNA autoantibodyBiomarkersMicroRNAsMIRN183 microRNA, human

Identifiers

PMID34036107
PMCPMC8124875
OpenAlexW3163304342

What OpenQuestion holds

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LicenceCC BY
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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.