Evidence map›Paper›PMID 10377169›Full record

ArticleThe Journal of clinical investigation1999

Susceptibility of lamivudine-resistant hepatitis B virus to other reverse transcriptase inhibitors.

S K Ono-Nita, N Kato, Y Shiratori, K H Lan, H Yoshida, F J Carrilho, M Omata

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

22 citing papers in PubMed, 132 citations in OpenAlex.

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  7. Current status of antiviral therapy for hepatitis B.Therapeutic advances in gastroenterology · 2008
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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

7 authors at 1 institution in 1 country.

S K Ono-NitaDepartment of Gastroenterology, Faculty of Medicine, University of Tokyo, Japan.
N Kato
Y Shiratori
K H Lan
H Yoshida
F J Carrilho
M Omata
The University of Tokyo · JP

Funding

Wellcome Trust
6 · The paper itself

Abstract

The emergence of resistant hepatitis B virus (HBV), with mutations in the YMDD motif of the polymerase gene after treatment with lamivudine, is becoming an important clinical problem. In this study, susceptibility of wild-type and lamivudine-resistant HBV M552I, M552V, and L528M/M552V mutants to other reverse transcriptase inhibitors was investigated by transient transfection of full-length HBV DNA into human hepatoma cells. HBV DNA replication was monitored by Southern blot hybridization, which showed the presence of a single-stranded band (representative of the HBV replicative intermediates) in the drug-free, wild-type HBV-transfected cells. This band was diminished in the samples of wild-type HBV DNA treated with either lamivudine, adefovir, or lobucavir. The band intensities from the lamivudine-resistant mutants were not decreased by treatment with lamivudine, but were decreased by the treatments with adefovir or lobucavir. In contrast, penciclovir and nevirapine did not diminish the intensity of the single-stranded band of wild-type HBV or the lamivudine-resistant mutants. These results demonstrate that lamivudine-resistant HBV is susceptible to adefovir and lobucavir. Lamivudine-resistant HBV should be treated with adefovir or lobucavir, and combination therapy with lamivudine and adefovir/lobucavir may prevent the emergence of lamivudine-resistant HBV.

Indexed as

OrganophosphonatesAcyclovirAdenineCarcinoma, HepatocellularDrug Resistance, MicrobialGuanineHepatitis B virusHumansLamivudineMutagenesis, Site-DirectedNevirapineReverse Transcriptase InhibitorsTransfectionTumor Cells, CulturedAcycloviradefovirAdenineGuanineLamivudinelobucavirNevirapineOrganophosphonatespenciclovirReverse Transcriptase Inhibitors

Identifiers

PMID10377169
PMCPMC408383
OpenAlexW2135638902

What OpenQuestion holds

Textmetadata
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.