Evidence map›Paper›PMID 38355214›Full record

ArticleLupus science & medicine2024

Potential involvement of circulating exosomal miRNA-146a in disease activity and

Poorichaya Somparn, Aunaymon Srichaimongkol, Suwaphit Jungjing, Bunsita Wanthong, Saharat Nanthawong, Leelahavanichkul Asada, Marut Tangwattanachuleepron, Pornpimol Rianthavorn

Open access · goldAbstract read
In one paragraph

Article in Lupus science & medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. 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

8 authors at 2 institutions in 1 country.

Poorichaya SomparnCenter of Excellence in Systems Biology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.ORCID 0000-0002-7422-1135
Aunaymon SrichaimongkolMaster of Science, Major in Medical Sciences, COMMON COURSE, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Suwaphit JungjingMaster of Science, Major in Medical Sciences, COMMON COURSE, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Bunsita WanthongFaculty of Allied Health Sciences, Burapha University, Chonburi, Thailand.
Saharat NanthawongCenter of Excellence in Systems Biology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Leelahavanichkul AsadaCenter of Excellence on Translational Research in Inflammation and Immunology, Department of Microbiology, Chulalongkorn University, Bangkok, Thailand.
Marut Tangwattanachuleepron *Faculty of Allied Health Sciences, Burapha University, Chonburi, Thailand pornpimol.r@chula.ac.th tp.marut@gmail.com.
Pornpimol Rianthavorn *Department of Pediatrics, Chulalongkorn University, Bangkok, Thailand pornpimol.r@chula.ac.th tp.marut@gmail.com.ORCID 0000-0003-2671-7416
Chulalongkorn University · THBurapha University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundJuvenile SLE (JSLE) is a complex autoimmune disorder that predominantly affects children and adolescents with several unique challenges, and microRNA-146a (miRNA-146a) might be an interesting anti-inflammatory molecule. Because exosomes in the blood might protect miRNAs, the association between circulating exosomal miRNA-146a and lupus proinflammatory genes, such as

methodsBlood samples from 12 patients were collected every 3 months until 1 year with the recorded disease activity, and quantitative real-time PCR was used to determine the circulating exosomal miRNA-146a and the gene expression (

resultsThe mean age was 12.60±0.43 years at diagnosis and all patients had a complete response at 12 months. According to the nanoparticle tracking analysis, the abundance of exosomes was significantly lower at 3, 6 and 12 months compared with 0 months, while the level of circulating exosomal miRNA-146a was significantly higher at 12 months than at diagnosis (p<0.001). There was a negative correlation between the level of circulating exosomal miRNA-146a expression and the level of

conclusionThis suggests that miRNA-146a might serve as a non-invasive biomarker to evaluate the response to treatment in patients with juvenile lupus nephritis.

Indexed as

Lupus Erythematosus, SystemicLupus NephritisMicroRNAsAdolescentChildGene ExpressionHumansIntracellular Signaling Peptides and ProteinsLeukocytes, MononuclearRNA, MessengerTNF Receptor-Associated Factor 6Intracellular Signaling Peptides and ProteinsMicroRNAsMIRN146 microRNA, humanRNA, MessengerTifab protein, humanTNF Receptor-Associated Factor 6InflammationLupus Erythematosus, SystemicTumor Necrosis Factor Receptor-Associated Peptides and Proteins

Identifiers

PMID38355214
PMCPMC10868173
OpenAlexW4391808950

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.