Evidence map›Paper›PMID 31886206›Full record

Trial reportBioMed research international2019

Genotypes and Hot Spot Mutations of Hepatitis B Virus in Northwest Chinese Population and Its Correlation with Diseases Progression.

Wei Wang, Yi Shu, Han Bao, Wenliang Zhao, Weihua Wang, Qin Wang, Xiaoying Lei, Daxiang Cui, Zhen Yan

Open access · hybridAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in BioMed research international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Review
  6. Detection of Hepatitis B Virus M204V Mutation Quantitatively via Real-time PCR.Journal of clinical and translational hepatology · 2021
    Article
  7. Article
  8. Hepatitis B Virus: From Diagnosis to Treatment.Polish journal of microbiology · 2020
    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

9 authors at 2 institutions in 1 country.

Wei Wang *The State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.ORCID https://orcid.org/0000-0001-5850-9107
Yi Shu *The State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.
Han BaoThe State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.
Wenliang ZhaoThe State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.
Weihua WangThe State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.
Qin WangThe State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.
Xiaoying LeiThe State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.
Daxiang CuiDepartment of Bio-Nano Science and Engineering, Key Laboratory for Thin Film and Microfabrication of Ministry of Education, Institute of Micro-Nano Science and Technology, Shanghai Jiao Tong University, Shanghai 200240, China.ORCID https://orcid.org/0000-0003-4513-905X
Zhen YanThe State Key Laboratory of Cancer Biology, Air Force Military Medical University, Xi'an 710032, China.ORCID https://orcid.org/0000-0001-6068-9645
State Key Laboratory of Cancer BiologyShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis B virus (HBV) infection is a critical incentive for chronic hepatitis B (CHB), liver cirrhosis (LC), and hepatocellular carcinoma (HCC). Different genotypes and genome mutations of HBV have been found to be related to the progression of these liver diseases. However, their clinical significance is still under debate. The objective of this study was to determine the association of HBV genotypes and hot spot mutations in the reverse transcriptase (RT) and basal core promoter-precore (BCP-PreC) region with HBV-infected diseases in a northwest Chinese population. HBV genotyping and DNA sequencing were performed in samples of 980 patients. Appropriate statistical methods were adopted to assess HBV genetic features and its clinical association. It was found that the prevalent HBV genotype in northwestern Chinese patients was HBV/C (61.33%), followed by HBV/B (36.63%). In RT region, in addition to the reported nucleoside analogue- (NA-) resistance missense mutations, new silent mutations at rt169 and rt180 were found to raise the risk of HCC in patients with HBV/C. And the heterozygous mutation status of rt169/rt180 was associated with the increased risk of both HCC and NA resistance (OR > 1,

Indexed as

GenotypeMutationAdultAsian PeopleCarcinoma, HepatocellularChinaDisease ProgressionDNA, ViralFemaleHepatitis B, ChronicHepatitis B virusHumansLiver CirrhosisLiver NeoplasmsMaleMiddle AgedDNA, Viral

Identifiers

PMID31886206
PMCPMC6925797
OpenAlexW3003908521

What OpenQuestion holds

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LicenceCC BY
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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.