Evidence map›Paper›PMID 30482723›Full record

ArticleEBioMedicine2018

Circulating miRNAs as footprints for liver fibrosis grading in schistosomiasis.

Pengfei Cai, Yi Mu, Remigio M Olveda, Allen G Ross, David U Olveda, Donald P McManus

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

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  9. Serum non-coding RNAs for diagnosis and stage of liver fibrosis.Journal of clinical laboratory analysis · 2022
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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 3 countries.

Pengfei CaiMolecular Parasitology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Australia. Electronic address: Pengfei.Cai@qimrberghofer.edu.au.
Yi MuMolecular Parasitology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Remigio M OlvedaDepartment of Health, Research Institute for Tropical Medicine, Manila, Philippines.
Allen G RossMenzies Health Institute Queensland, Griffith University, Gold Coast, Australia; icddr b, Dhaka, Bangladesh.
David U OlvedaMenzies Health Institute Queensland, Griffith University, Gold Coast, Australia.
Donald P McManusMolecular Parasitology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Australia. Electronic address: Don.McManus@qimrberghofer.edu.au.
QIMR Berghofer Medical Research Institute · AUGriffith University · AUInternational Centre for Diarrhoeal Disease Research · BDResearch Institute for Tropical Medicine · PH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic infection with Schistosoma japonicum or S. mansoni results in hepatic fibrosis of the human host. Staging fibrosis is crucial for the prognosis and to determine the rapid need of treatment in patients with schistosomiasis.

methodsTo establish whether there is a correlation between circulating microRNA (miRNA) level and fibrosis progression in schistosomiasis, ten miRNAs were selected to assess their potential in grading schistosomiasis liver fibrosis. This was done firstly in two mouse strains (C57BL/6 and BALB/c) to determine the temporal expression profiles in serum over the course of S. japonicum infection, and then within a cohort of 163 schistosomiasis japonica patients with different grades of liver fibrosis. FINDING: Four miRNAs (miR-150-5p, let-7a-5p, let-7d-5p and miR-146a-5p) were able to distinguish patients with mild versus severe fibrosis. The level of serum miR-150-5p showed the most promising potential for grading hepatic fibrosis in schistosomiasis. The diagnostic performance of miR-150-5p in discriminating mild from severe fibrosis is comparable with that of the ELF test and serum HA level. In addition, the serum levels of the four miRNAs rebounded in infected C57BL/6 mice, after 6 months post treatment, following the regression of liver fibrosis, thereby providing further support for the utility of these miRNAs in grading schistosomal hepatic fibrosis.

interpretationCirculating miRNAs can be a supplementary tool for assessing hepatic fibrosis in human schistosomiasis. FUND: National Health and Medical Research Council (NHMRC) of Australia (APP1102926, APP1037304 and APP1098244).

Indexed as

Schistosoma japonicumSchistosoma mansoniAdultAnimalsCell-Free Nucleic AcidsFemaleHumansLiver CirrhosisMaleMice, Inbred BALB CMicroRNAsMiddle AgedSchistosomiasis japonicaSchistosomiasis mansoniCell-Free Nucleic AcidsMicroRNAsBiomarkerhepatic fibrosismicroRNAsSchistosoma japonicumschistosome

Identifiers

PMID30482723
PMCPMC6286190
OpenAlexW2898149625

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.