Evidence map›Paper›PMID 35157730›Full record

ArticlePloS one2022

Serum miR-192-5p levels predict the efficacy of pegylated interferon therapy for chronic hepatitis B.

Yoshihito Nagura, Kentaro Matsuura, Etsuko Iio, Koji Fujita, Takako Inoue, Akihiro Matsumoto, Eiji Tanaka, Shuhei Nishiguchi, Jong-Hon Kang, Takeshi Matsui and 9 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Hepatitis B Virus and microRNAs: A Bioinformatics Approach.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Review
  8. 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

19 authors at 12 institutions in 1 country.

Yoshihito NaguraDepartments of Virology & Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.
Kentaro MatsuuraDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.
Etsuko IioDepartments of Virology & Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.
Koji FujitaDepartment of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Miki, Kagawa, Japan.
Takako InoueDepartment of Clinical Laboratory Medicine, Nagoya City University Hospital, Nagoya, Aichi, Japan.
Akihiro MatsumotoDepartment of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.
Eiji TanakaDepartment of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Nagano, Japan.
Shuhei NishiguchiDivision of Hepatobiliary and Pancreatic Disease, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
Jong-Hon KangDivision of Center for Gastroenterology, Teine Keijinkai Hospital, Sapporo, Hokkaido, Japan.
Takeshi MatsuiDivision of Center for Gastroenterology, Teine Keijinkai Hospital, Sapporo, Hokkaido, Japan.
Masaru EnomotoDepartment of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Osaka, Japan.
Hiroki IkedaDivision of Gastroenterology and Hepatology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Tsunamasa WatanabeDivision of Gastroenterology and Hepatology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan.
Chiaki OkuseDivision of General Internal Medicine, Department of Internal Medicine, Kawasaki Municipal Tama Hospital, Kawasaki, Kanagawa, Japan.
Masataka TsugeDepartment of Gastroenterology and Metabolism, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Hiroshima, Japan.ORCID 0000-0001-7591-8287
Masanori AtsukawaDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Nippon Medical School, Tokyo, Japan.ORCID 0000-0003-3374-7111
Masakuni TateyamaDepartment of Gastroenterology and Hepatology Faculty of Life Sciences, Kumamoto University, Kumamoto, Kumamoto, Japan.
Hiromi KataokaDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.ORCID 0000-0001-9491-0723
Yasuhito TanakaDepartments of Virology & Liver Unit, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.ORCID 0000-0002-2473-6966
Nagoya City University · JPShinshu University · JPSt. Marianna University School of Medicine · JPTeine Keijinkai Hospital · JPHiroshima University · JPHyogo Medical University · JPKagawa University · JPKawasaki Municipal Hospital · JPKumamoto University · JPNagoya City University Hospital · JPNippon Medical School · JPOsaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We examined the association between serum miRNA (-192-5p, -122-3p, -320a and -6126-5p) levels and the efficacy of pegylated interferon (Peg-IFN) monotherapy for chronic hepatitis B (CHB) patients. We enrolled 61 CHB patients treated with Peg-IFNα-2a weekly for 48 weeks, of whom 12 had a virological response (VR) and 49 did not VR (non-VR). A VR was defined as HBV DNA < 2,000 IU/ml, hepatitis B e antigen (HBeAg)-negative, and nucleos(t)ide analogue free at 48 weeks after the end of treatment. The non-VR group showed a significantly higher HBeAg-positivity rate, ALT, HBV DNA, and serum miR-192-5p levels at baseline (P = 0.024, P = 0.020, P = 0.007, P = 0.021, respectively). Serum miR-192-5p levels at 24-weeks after the start of treatment were also significantly higher in the non-VR than the VR group (P = 0.011). Multivariate logistic regression analysis for predicting VR showed that miR-192-5p level at baseline was an independent factor (Odds 4.5, P = 0.041). Serum miR-192-5p levels were significantly correlated with the levels of HBV DNA, hepatitis B core-related antigen, and hepatitis B surface antigen (r = 0.484, 0.384 and 0.759, respectively). The serum miR-192-5p level was useful as a biomarker for the therapeutic efficacy of Peg-IFN in CHB treatment.

Indexed as

AdultAntiviral AgentsBiomarkersCase-Control StudiesDNA, ViralFemaleGene Expression RegulationHepatitis B, ChronicHepatitis B virusHumansInterferon-alphaMaleMicroRNAsMiddle AgedPolyethylene GlycolsRecombinant ProteinsAntiviral AgentsBiomarkersDNA, ViralInterferon-alphaMicroRNAsMIRN192 microRNA, humanpeginterferon alfa-2aPolyethylene GlycolsRecombinant Proteins

Identifiers

PMID35157730
PMCPMC8843190
OpenAlexW4225596698

What OpenQuestion holds

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LicenceCC BY
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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.