Evidence map›Paper›PMID 24551214›Full record

ArticlePloS one2014

Analysis of hepatitis B virus intrahepatic covalently closed circular DNA and serum viral markers in treatment-naive patients with acute and chronic HBV infection.

Weijie Li, Jingmin Zhao, Zhengsheng Zou, Yan Liu, Baosen Li, Ying Sun, Xiaodong Li, Shuhong Liu, Shaoping Cai, Weiming Yao and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The role of HBV cccDNA in occult hepatitis B virus infection.Molecular and cellular biochemistry · 2023
    Review
  4. Follow-Up of Newborns with Hepatitis B Antigenemia.Infectious diseases and therapy · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Guideline of Prevention and Treatment for Chronic Hepatitis B (2015 Update).Journal of clinical and translational hepatology · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. [The guideline of prevention and treatment for chronic hepatitis B: a 2015 update].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2015
    Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

  • Erratum issued
    Yao, Weimin [corrected to Yao, Weiming]
5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Weijie LiDepartment of Microbiology, Peking University Health Science Center, Beijing, China ; Institute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Jingmin ZhaoDepartment of Pathology, Beijing 302 Hospital, Beijing, China.
Zhengsheng ZouInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Yan LiuInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Baosen LiInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Ying SunInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Xiaodong LiInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Shuhong LiuDepartment of Pathology, Beijing 302 Hospital, Beijing, China.
Shaoping CaiInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Weiming Yao
Weimin YaoInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Shaojie XinInstitute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
Fengmin LuDepartment of Microbiology, Peking University Health Science Center, Beijing, China.
Dongping XuDepartment of Microbiology, Peking University Health Science Center, Beijing, China ; Institute of Infectious Diseases and Medical Center for Liver Failure, Beijing 302 Hospital, Beijing, China.
302 Military Hospital of China · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to investigate the relationships of intrahepatic cccDNA with serum HBsAg and with HBV DNA in treatment-naive patients throughout acute and chronic HBV infection.

methodsA total of 120 patients who had a liver biopsy were enrolled, including 19 with acute hepatitis B (AHB), and 101 patients with chronic HBV infection (CHB) of whom were 10 in immune-tolerant (IT) phase, 59 in immune-clearance (IC) phase, 8 in low-replicative (LR) phase, and 24 in HBeAg-negative hepatitis (ENH) phase. Intrahepatic cccDNA, serum HBsAg and serum HBV DNA levels were comparatively analyzed.

resultsThe median intrahepatic cccDNA levels were 0.18 4.80, 3.81, 0.22 and 0.97 copies/cell for patients with AHB, CHB-IT, CHB-IC, CHB-LR, and CHB-ENH, respectively. In AHB patients, intrahepatic cccDNA was positively correlated with serum HBsAg (r = 0.665, P = 0.003), as well as serum HBV DNA (r = 0.536, P = 0.022). In CHB patients, intrahepatic cccDNA was positively correlated with serum HBsAg in the IC phase (r = 0.392, P = 0.005), and with serum HBV DNA in the IC phase (r = 0.301, P = 0.036) and ENH phase (r = 0.588, P = 0.013). HBV replicative efficiency, defined as the ratio of serum HBV DNA to intrahepatic cccDNA, was obviously lower in AHB and CHB-LR patients than in CHB-IT, CHB-IC and CHB-ENH patients (0.70 and 0.53 vs. 1.12, 1.09 and 0.99, P<0.001, values were logarithmic transformed for analysis). In CHB-IC patients, HBV replicative efficiency was positively correlated with histological activity index of liver inflammation (r = 0.308, P = 0.009).

conclusionSerum HBsAg and HBV DNA levels may reflect the amount of active intrahepatic cccDNA in treatment-naive AHB and CHB-IC patients. Reduced intrahepatic cccDNA and HBV replicative efficiency may imply effective immune control of HBV infection.

Indexed as

Acute DiseaseAdultBiomarkersChildDNA, CircularDNA, ViralFemaleHepatitis B, ChronicHepatitis B Surface AntigensHepatitis B virusHumansImmune ToleranceLiverMaleSeverity of Illness IndexVirus ReplicationBiomarkersDNA, CircularDNA, ViralHepatitis B Surface Antigens

Identifiers

PMID24551214
PMCPMC3923869
OpenAlexW2084643412

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Registered trials

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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.