Evidence map›Paper›PMID 27054010›Full record

ArticleElectronic physician2016

The Role of MicroRNAs in Response to Interferon Treatment of Chronic Hepatitis C patients.

Eman El-Ahwany, Faten Nagy, Mona Zoheiry, Maged ELGhannam, Mohamed Shemis, Mohamed Aboul-Ezz, Suher Zada

Abstract read
In one paragraph

Article in Electronic physician, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Eman El-AhwanyImmunology Department, Theodor Bilharz Research Institute, Giza, Egypt.
Faten NagyImmunology Department, Theodor Bilharz Research Institute, Giza, Egypt.
Mona ZoheiryImmunology Department, Theodor Bilharz Research Institute, Giza, Egypt.
Maged ELGhannamHepato-gastroenterology Department, Theodor Bilharz Research Institute, Giza, Egypt.
Mohamed ShemisBiochemistry Departm, Theodor Bilharz Research Institute, Giza, Egypt.
Mohamed Aboul-EzzHepato-gastroenterology Department, Theodor Bilharz Research Institute, Giza, Egypt.
Suher ZadaBiology Department, the American University in Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTreatment of HCV using a combination of pegylated interferon (PEG-IFN) and ribavirin fails in about 40% of the patients with HCV genotype 4 infections, and it is physically and economically demanding. Thus, it is highly important to identify factors that can help to predict the likelihood that a patient will respond to this treatment.

methodsIn this study, five miRNAs, i.e., miRNA-122, miRNA-199, miRNA-192, miRNA-30, and miRNA-128, were selected according to previous studies that demonstrated their noticeable functions in viral replication, indicating that they potentially could be used by host cells to control viral infections. The five miRNAs were measured using real-time, reverse transcription-polymerase chain reactions. The data were analyzed using the t-test and chi-squared test.

resultsWe found that the expression level of miRNA-122 was significantly increased in the responders' group (p < 0.01) over that in the non-responders' groups before and after treatment; both increased significantly (p < 0.01) compared with the normal control group.

conclusionmiR-122 might be a useful predictor for virological responses to treatment with PEG-interferon plus ribavirin therapy in patients with HCV.

Indexed as

Chronic Hepatitis CHCVInterferonmicroRNApegylated interferon

Identifiers

PMID27054010
PMCPMC4821316

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