Evidence map›Paper›PMID 35524830›Full record

ArticleCurrent microbiology2022

hsa-miR-17-5p: A Possible Predictor of Ombitasvir/Paritaprevir/Ritonavir + Dasabuvir ± Ribavirin Therapy Efficacy in Hepatitis C Infection.

Zehra Öksüz, Enver Üçbilek, Mehmet Sami Serin, Serkan Yaraş, Gülhan Örekici Temel, Orhan Sezgin

Abstract read
PubMed Publisher
In one paragraph

Article in Current microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 1 country.

Zehra ÖksüzDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, Mersin University, Mersin, Turkey. zehraoksz@gmail.com.ORCID http://orcid.org/0000-0002-1542-0556
Enver ÜçbilekDepartment of Gastroenterology, Faculty of Medicine, Mersin University, Mersin, Turkey.ORCID http://orcid.org/0000-0002-2935-5580
Mehmet Sami SerinDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.ORCID http://orcid.org/0000-0002-5113-5509
Serkan YaraşDepartment of Gastroenterology, Faculty of Medicine, Mersin University, Mersin, Turkey.ORCID http://orcid.org/0000-0003-1404-7515
Gülhan Örekici TemelDepartment of Biostatistics, Faculty of Medicine, Mersin University, Mersin, Turkey.ORCID http://orcid.org/0000-0002-2835-6979
Orhan SezginDepartment of Gastroenterology, Faculty of Medicine, Mersin University, Mersin, Turkey.ORCID http://orcid.org/0000-0002-6704-4716
Mersin Üniversitesi · TR

Funding

Türkiye Bilimsel ve Teknolojik Araştirma Kurumu 218S809
6 · The paper itself

Abstract

Although persistent sustained viral response rates are increased in hepatitis C infection following administration of direct-acting antiviral (DAA) agents, the pre-use predictive parameters of these antivirals and the clinical progression in patients post-treatment remain unknown. To obtain data pertaining to the predictive parameters prior to the use of ombitavir/paritaprevir/ritonavir + dasabuvir and the clinical progression in patients following antiviral treatment. The expression profiles of miR-223-3p, miR-17-5p, miR-24-3p, and TLR2 - 196 to - 174 del/ins polymorphisms from the blood/serum of 34 hepatitis C virus (HCV)-infected patients pre- and post-ombitavir/paritaprevir/ritonavir + dasabuvir treatment were determined by RT-qPCR. The expression levels of miR-17-5p (P < 0.001) and miR-24-3p (P = 0.011) were significantly downregulated post-treatment as compared with those pre-treatment; however, there was no significant difference between these two groups in terms of miR-223-3p expression. In addition, there was no significant difference in TLR2 genotype or allele distribution between pre-and post-treatment (P > 0.05); nevertheless, the TLR2 del allele was decreased post-treatment (16.2%) as compared with that pre-treatment (19.1%), although the difference was not statistically significant. Moreover, a significant difference was found between the mRNA levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and HCV RNA pre-and post-treatment (P < 0.05). Further, miR-17-5p expression correlated with both ALT and AST mRNA levels post-treatment (P.

Indexed as

Antiviral AgentsHepatitis CMacrocyclic CompoundsMicroRNAs2-NaphthylamineAnilidesCarbamatesCyclopropanesDrug Therapy, CombinationHumansLactams, MacrocyclicProlineRibavirinRitonavirRNA, MessengerSulfonamides2-NaphthylamineAnilidesAntiviral AgentsCarbamatesCyclopropanesdasabuvirLactams, MacrocyclicMacrocyclic CompoundsMicroRNAsMIRN17 microRNA, humanombitasvirparitaprevirProlineRibavirinRitonavirRNA, MessengerSulfonamidesToll-Like Receptor 2UracilValine

Identifiers

PMID35524830
OpenAlexW4229012092

What OpenQuestion holds

Textmetadata
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.