Evidence map›Paper›PMID 27626177›Full record

ArticleOncotarget2016

Interferon-stimulated gene 15 in hepatitis B-related liver diseases.

Nghiem Xuan Hoan, Hoang Van Tong, Dao Phuong Giang, Nguyen Linh Toan, Christian G Meyer, C-Thomas Bock, Peter G Kremsner, Le Huu Song, Thirumalaisamy P Velavan

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Serum NOX2 as a new biomarker candidate for HBV-related disorders.American journal of translational research · 2018
    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 at 5 institutions in 2 countries.

Nghiem Xuan HoanInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Hoang Van TongInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Dao Phuong GiangInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Nguyen Linh ToanVietnamese-German Center for Medical Research, Hanoi, Vietnam.
Christian G MeyerInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
C-Thomas BockDepartment of Infectious Diseases, Robert Koch Institute, Berlin, Germany.
Peter G KremsnerInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Le Huu Song108 Military Central Hospital, Hanoi, Vietnam.
Thirumalaisamy P VelavanInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
108 Military Central Hospital · VNUniversity of Tübingen · DEVietnamese - German Center of Excellence in Medical Research · VNVietnam Military Medical University · VNRobert Koch Institute · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigates the association of Interferon-stimulated gene 15 (ISG15) polymorphisms, ISG15 serum levels and expression with HBV-related liver diseases. The ISG15 promoter and the two exons of the gene were screened for polymorphisms in 766 HBV-infected patients and in 223 controls. Soluble ISG15 levels were measured by ELISA. ISG15 mRNA expression was quantified by qRT-PCR in 36 tumor and adjacent non-tumor tissues. The exon 2 allele rs1921A was found associated with decreased progression of HBV-related liver diseases (LC vs. CHB: OR = 0.6, 95%CI = 0.4-0.8, adjusted P = 0.003; HCC vs. CHB: OR = 0.6, 95%CI = 0.4-0.9, adjusted P = 0.005). The rs1921AA genotype was associated with low levels of AST, ALT and total bilirubin, but with high prothrombin levels (P < 0.05). ISG15 serum levels were higher among HBV patients compared to controls (P < 0.0001) and positively associated with HBV-related liver diseases, with highest levels among LC patients. ISG15 levels were correlated with HBV-DNA loads (P = 0.001). In non-tumor tissues from HCC patients, ISG15 mRNA expression was increased in HBV compared to non-HBV infection (P = 0.016). The ISG15 rs1921 variant and ISG15 expression are associated with HBV-related liver diseases. Taken together, ISG15 appears to be a proviral factor involved in HBV replication and triggering progression of HBV-related liver diseases.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedAged, 80 and overCarcinoma, HepatocellularCytokinesFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHepatitis B, ChronicHepatitis B virusHumansLiver CirrhosisLiver NeoplasmsCytokinesISG15 protein, humanUbiquitinsHBV infectionISG15ISG15 polymorphismISGlationliver diseasesPathology Section

Identifiers

PMID27626177
PMCPMC5356518
OpenAlexW2515424962

What OpenQuestion holds

Textmetadata
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.