Evidence map›Paper›PMID 32747646›Full record

ArticleScientific reports2020

Detectable HBV DNA during nucleos(t)ide analogues stratifies predictive hepatocellular carcinoma risk score.

Shun Kaneko, Masayuki Kurosaki, Kouji Joko, Hiroyuki Marusawa, Masahiko Kondo, Yuji Kojima, Yasushi Uchida, Hiroyuki Kimura, Keiji Tsuji, Hitoshi Yagisawa and 10 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Magnetic resonance elastography for the prediction of hepatocellular carcinoma in chronic hepatitis B.JGH open : an open access journal of gastroenterology and hepatology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
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

20 authors at 15 institutions in 1 country.

Shun KanekoDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1, Kyonan-cho, Musashino-shi, Tokyo, 180-8610, Japan.
Masayuki KurosakiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1, Kyonan-cho, Musashino-shi, Tokyo, 180-8610, Japan.
Kouji JokoCenter for Liver-Biliary-Pancreatic Diseases, Matsuyama Red Cross Hospital, Ehime, Japan.
Hiroyuki MarusawaDepartment of Gastroenterology, Japanese Red Cross Osaka Hospital, Osaka, Japan.
Masahiko KondoDepartment of Gastroenterology, Japanese Red Cross Otsu Hospital, Shiga, Japan.
Yuji KojimaDepartment of Gastroenterology, Japanese Red Cross Ise Hospital, Mie, Japan.
Yasushi UchidaDepartment of Gastroenterology, Japanese Red Cross Matsue Hospital, Shimane, Japan.
Hiroyuki KimuraDepartment of Gastroenterology, Japanese Red Cross Kyoto Daiichi Hospital, Kyoto, Japan.
Keiji TsujiDepartment of Gastroenterology, Hiroshima Red Cross Hospital and Atomic-Bomb Survivors Hospital, Hiroshima, Japan.
Hitoshi YagisawaDepartment of Gastroenterology, Japanese Red Cross Akita Hospital, Akita, Japan.
Atsunori KusakabeDepartment of Gastroenterology, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.
Haruhiko KobashiDepartment of Hepatology, Japanese Red Cross Okayama Hospital, Okayama, Japan.
Takehiro AkahaneDepartment of Gastroenterology, Japanese Red Cross Ishinomaki Hospital, Miyagi, Japan.
Nobuharu TamakiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1, Kyonan-cho, Musashino-shi, Tokyo, 180-8610, Japan.
Sakura KirinoDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1, Kyonan-cho, Musashino-shi, Tokyo, 180-8610, Japan.
Takehiko AbeDepartment of Gastroenterology, Japanese Red Cross Maebashi Hospital, Gunma, Japan.
Hideo YoshidaDepartment of Gastroenterology, Japanese Red Cross Medical Center, Tokyo, Japan.
Tomomichi MatsushitaDepartment of Gastroenterology, Japanese Red Cross Gifu Hospital, Gifu, Japan.
Chitomi HasebeDepartment of Gastroenterology, Japanese Red Cross Asahikawa Hospital, Hokkaido, Japan.
Namiki IzumiDepartment of Gastroenterology and Hepatology, Musashino Red Cross Hospital, 1-26-1, Kyonan-cho, Musashino-shi, Tokyo, 180-8610, Japan. izumi012@musashino.jrc.or.jp.
Musashino Red Cross Hospital · JPAkita Red Cross Hospital · JPGifu Red Cross Hospital · JPHiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital · JPIse Red Cross Hospital · JPJapanese Red Cross Asahikawa Hospital · JPJapanese Red Cross Medical Center · JPJapanese Red Cross Nagoya Daini Hospital · JPKyoto first Red Cross hospital · JPMaebashi Red Cross Hospital · JPMatsue Red Cross Hospital · JPMatsuyama Red Cross Hospital · JPOkayama Red Cross General Hospital · JPOsaka Hospital · JPOtsu Red Cross Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleos(t)ide analogs (NA) suppress hepatitis B virus (HBV) replication and reduce the risk of hepatocellular carcinoma (HCC). However, NA cannot suppress carcinogenesis completely in patients with chronic hepatitis B. The aims of this study were to identify risk factors for HCC and develop a refined carcinogenesis prediction model. Patients receiving NA therapy (n = 1,183) were recruited retrospectively from the 16 hospitals. All patients had been receiving NA continuously for more than 1 year until the end of the follow-up. During a median follow-up of 4.9 (1.0-12.9) years, 52 (4.4%) patients developed HCC. A multivariate analysis revealed that male gender, older age, lower platelet counts at the baseline, and detectable HBV DNA during NA therapy were independent predictive factors of HCC development. The PAGE-B score was calculated by using these factors. 240 (20.3%), 661 (55.9%), and 282 (23.8%) patients were classified into low-, intermediate-, and high-risk groups, respectively. In the intermediate- and high-risk group, detectable HBV DNA was significantly associated with a higher risk of HCC development compared with continuously undetectable HBV DNA, respectively (HR 3.338; 95% CI 1.045-10.66/HR 3.191; 95% CI 1.543-6.597). PAGE-B-DNA, which is the combined PAGE-B and HBV DNA status, was valuable for a more refined stratification of PAGE-B.

Indexed as

Carcinoma, HepatocellularDNA, ViralFemaleHepatitis B virusHumansIncidenceLiver NeoplasmsMaleMiddle AgedNucleotidesProportional Hazards ModelsRegression AnalysisRisk FactorsDNA, ViralNucleotides

Identifiers

PMID32747646
PMCPMC7400741
OpenAlexW3046905428

What OpenQuestion 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 OpenQuestion graph.