Evidence map›Paper›PMID 36834868›Full record

ArticleInternational journal of molecular sciences2023

Circulating miR-122-5p, miR-92a-3p, and miR-18a-5p as Potential Biomarkers in Human Liver Transplantation Follow-Up.

Cristina Morsiani, Salvatore Collura, Federica Sevini, Erika Ciurca, Valentina Rosa Bertuzzo, Claudio Franceschi, Gian Luca Grazi, Matteo Cescon, Miriam Capri

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
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

9 authors.

Cristina MorsianiDIMEC-Department of Medicine and Surgery, University of Bologna, Via S. Giacomo 12, 40126 Bologna, Italy.
Salvatore ColluraDIMEC-Department of Medicine and Surgery, University of Bologna, Via S. Giacomo 12, 40126 Bologna, Italy.ORCID 0000-0002-6262-8173
Federica SeviniDIMEC-Department of Medicine and Surgery, University of Bologna, Via S. Giacomo 12, 40126 Bologna, Italy.
Erika CiurcaDIMEC-Department of Medicine and Surgery, University of Bologna, Via S. Giacomo 12, 40126 Bologna, Italy.
Valentina Rosa BertuzzoHepatobiliary and Transplant Surgery Unit, IRCCS, Universitaria Sant'Orsola Hospital, University of Bologna, 40138 Bologna, Italy.ORCID 0000-0002-4339-4877
Claudio FranceschiLaboratory of Systems Medicine of Healthy Aging, Department of Applied Mathematics, Lobachevsky University, 603022 Nizhny Novgorod, Russia.
Gian Luca GraziHepatopancreatobiliary Surgery, IRCCS-Regina Elena National Cancer Institute, 00114 Rome, Italy.
Matteo CesconHepatobiliary and Transplant Surgery Unit, IRCCS, Universitaria Sant'Orsola Hospital, University of Bologna, 40138 Bologna, Italy.
Miriam CapriDIMEC-Department of Medicine and Surgery, University of Bologna, Via S. Giacomo 12, 40126 Bologna, Italy.ORCID 0000-0001-9077-0401

Funding

Ministero dell'Università e della Ricerca PRIN2008
6 · The paper itself

Abstract

The requirement of blood-circulating sensitive biomarkers for monitoring liver transplant (LT) is currently a necessary step aiming at the reduction of standard invasive protocols, such as liver biopsy. In this respect, the main objective of this study is to assess circulating microRNA (c-miR) changes in recipients' blood before and after LT and to correlate their blood levels with gold standard biomarkers and with outcomes such as rejection or complications after graft. An miR profile was initially performed; then, the most deregulated miRs were validated by RT-qPCR in 14 recipients pre- and post-LT and compared to a control group of 24 nontransplanted healthy subjects. MiR-122-5p, miR-92a-3p, miR-18a-5p, and miR-30c-5p, identified in the validation phase, were also analyzed considering an additional 19 serum samples collected from LT recipients and focusing on different follow-up (FU) times. The results showed significant, FU-related changes in c-miRs. In particular, miR-122-5p, miR-92a-3p, and miR-18a-5p revealed the same trend after transplantation and an increase in their level was found in patients with complications, independently from FU times. Conversely, the variations in the standard haemato-biochemical parameters for liver function assessment were not significant in the same FU period, confirming the importance of c-miRs as potential noninvasive biomarkers for monitoring patients' outcomes.

Indexed as

Circulating MicroRNALiver TransplantationMicroRNAsBiomarkersFollow-Up StudiesHumansBiomarkersCirculating MicroRNAMicroRNAsMIRN122 microRNA, humanMIRN18A microRNA, humanMIRN92 microRNA, humanfollow-up timingliver transplantmicroRNAsnoninvasive biomarkers

Identifiers

PMID36834868
PMCPMC9962619

What Socratic 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 Socratic graph.