ReviewWorld journal of gastroenterology2007
Future prospectives for the management of chronic hepatitis B.
Review in World journal of gastroenterology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
What it found
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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.
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.
Who cites it
12 citing papers in PubMed, 23 citations in OpenAlex.
- A novel method for diagnosing cirrhosis in patients with chronic hepatitis B: artificial neural network approach.Journal of medical systems · 2011Trial
- Circulating mitochondrial DNA content associated with the risk of liver cirrhosis: a nested case-control study.Digestive diseases and sciences · 2015Article
- Serum proteins in chronic hepatitis B patients treated with peginterferon alfa-2b.World journal of gastroenterology · 2013Article
- Changes of Some Hormones Levels in Patients With Hepatitis B Virus-Related Chronic Liver Disease.Gastroenterology research · 2013Article
- In vitro replication phenotype of a novel (-1G) hepatitis B virus variant associated with HIV co-infection.Journal of medical virology · 2012Article
- Anti-hepatitis B virus activity of chickweed [Stellaria media (L.) Vill.] extracts in HepG2.2.15 cells.Molecules (Basel, Switzerland) · 2012Article
- Classification of Traditional Chinese Medicine Syndromes in Patients with Chronic Hepatitis B by SELDI-Based ProteinChip Analysis.Evidence-based complementary and alternative medicine : eCAM · 2012Article
- The first transmembrane domain of the hepatitis B virus large envelope protein is crucial for infectivity.Journal of virology · 2009Article
- Baseline predictors of virological response for chronic hepatitis B patients.World journal of gastroenterology · 2009Article
- A new clade of hepatitis B virus subgenotype F1 from Peru with unusual properties.Virus genes · 2008Article
- Effect and mechanism of beta-L-D4A on DNA polymerase alpha.World journal of gastroenterology · 2007Article
- Interactions between buprenorphine and antiretrovirals: nucleos(t)ide reverse transcriptase inhibitors (NRTI) didanosine, lamivudine, and tenofovir.The American journal on addictionsArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
unlabelledChronic hepatitis B virus infection affects about 400 million people around the globe and causes approximately a million deaths a year. Since the discovery of interferon-alpha as a therapeutic option the treatment of hepatitis B has evolved fast and management has become increasingly complicated. The amount of viral replication reflected in the viral load (HBV-DNA) plays an important role in the development of cirrhosis and hepatocellular carcinoma. The current treatment modalities for chronic hepatitis B are immunomodulatory (interferons) and antiviral suppressants (nucleoside and nucleotide analogues) all with their own advantages and limitations. An overview of the treatment efficacy for both immunomodulatory as antiviral compounds is provided in order to provide the clinician insight into the factors influencing treatment outcome. With nucleoside or nucleotide analogues suppression of viral replication by 5-7 log(10) is feasible, but not all patients respond to therapy. Known factors influencing treatment outcome are viral load, ALT levels and compliance. Many other factors which might influence treatment are scarcely investigated. Identifying the factors associated with response might result in stopping rules, so treatment could be adapted in an early stage to provide adequate treatment and avoid the development of resistance. The efficacy of compounds for the treatment of mutant virus and the cross-resistance is largely unknown. However, genotypic and phenotypic testing as well as small clinical trials provided some data on efficacy in this population. Discontinuation of nucleoside or nucleotide analogues frequently results in viral relapse; however, some patients have a sustained response. Data on the risk factors for relapse are necessary in order to determine when treatment can be discontinued safely. IN
conclusionchronic hepatitis B has become a treatable disease; however, much research is needed to tailor therapy to an individual patient, to predict the sustainability of response and determine the best treatment for those failing treatment.
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Registered trials
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.