Evidence map›Paper›PMID 31695474›Full record

ArticlePharmacogenomics and personalized medicine2019

Genotypic Resistance Remains A Concern In Chronic Hepatitis B Patients With High Viral Load After Lamivudine And Adefovir Combination Therapy.

Meijin Huang, Jie Zhong, Chunlei Lu, Fenglian Deng, Li Li, Yixi Nong, Liudan Liang, Houji Qin, Yibin Deng

Open access · goldAbstract read
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
–field-weighted citation impact, top 83% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Meijin Huang *Department of Infectious Diseases, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Jie Zhong *Department of Neurology, The First Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi Province, People's Republic of China.
Chunlei LuDepartment of Infectious Diseases, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Fenglian DengDepartment of Infectious Diseases, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Li LiDepartment of Infectious Diseases, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Yixi NongDepartment of Infectious Diseases, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Liudan LiangDepartment of Infectious Diseases, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Houji QinDepartment of Infectious Diseases, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Yibin DengMedical Examination Center, Affiliated Hospital of Youjiang Nationalities Medical College, Baise City, Guangxi Province, People's Republic of China.
Youjiang Medical College for Nationalities · CNGuangxi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsPrevious studies have shown that baseline high viral load is closely related to treatment response in chronic hepatitis B (CHB). This study was designed to evaluate the differences of treatment responses between de novo lamivudine (LAM) plus adefovir (ADV) combination therapy compared with entecavir monotherapy (ETV).

methodsA total of 185 HBeAg-positive CHB patients with high viral load were enrolled and assigned to the LAM+ADV group (n=90) or ETV group (n=95). Clinical variables are extracted from medical records.

resultsNo significant differences in baseline variables were found between the two groups before antiviral treatment. After 104 weeks of antiviral therapy, the mean HBV DNA viral load in the LAM+ADV group decreased from 8.01±0.65 log

conclusionBoth de novo combination therapy of LAM+ADV and ETV monotherapy could effectively inhibit HBV replication in patients with high viral load. However, the rate of genotypic resistance in LAM+ADV treatment remains a concern. For CHB patients with high viral load, ETV treatment may be superior.

Indexed as

chronic hepatitis Bhigh viral loadnucleos(t)ide analogsvirologic response

Identifiers

PMID31695474
PMCPMC6814354
OpenAlexW2981193559

What OpenQuestion holds

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LicenceCC BY-NC
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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.