Evidence map›Paper›PMID 37703117›Full record

ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2023

Maternal A90V mutation in the PreS1 gene of sub-genotype C2 hepatitis B virus is associated with intrauterine transmission.

Linzhu Yi, Jiaxin Wu, Zhiqing Yang, Yandi Li, Jia Lian, Tian Yao, Shuying Feng, Bo Wang, Yongliang Feng, Suping Wang

Abstract read
In one paragraph

Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

The trial behind it

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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

2 citing papers in PubMed.

  1. Article
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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

10 authors.

Linzhu YiShanxi Medical University, Department of Epidemiology, Taiyuan, Shanxi, China.
Jiaxin WuShanxi Provincial Center for Disease Control and Prevention, Taiyuan, Shanxi, China.
Zhiqing YangShanxi Medical University, Department of Epidemiology, Taiyuan, Shanxi, China.
Yandi LiShanxi Medical University, Department of Epidemiology, Taiyuan, Shanxi, China.
Jia LianShanxi Medical University, Department of Epidemiology, Taiyuan, Shanxi, China.
Tian YaoShanxi Medical University, Department of Epidemiology, Taiyuan, Shanxi, China.
Shuying FengThird People's Hospital, Department of Obstetrics and Gynaecology, Taiyuan, Shanxi, China.
Bo WangThird People's Hospital, Department of Obstetrics and Gynaecology, Taiyuan, Shanxi, China.
Yongliang FengShanxi Medical University, Department of Epidemiology, Taiyuan, Shanxi, China.
Suping WangShanxi Medical University, Department of Epidemiology, Taiyuan, Shanxi, China.ORCID http://orcid.org/0000-0002-1476-5595

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PreS/S gene mutations could impact virus secretion, infection and immune evasion. However, the relationship between PreS/S mutations and intrauterine transmission has not yet been clarified. Thus, we aimed to explore the associations between PreS/S gene mutations of HBV isolated from mothers and intrauterine transmission. We analyzed the mutations of PreS/S regions of the HBV genome in mothers with HBV DNA levels ≥ 106 IU/mL whose neonates experienced HBV intrauterine transmission (transmission group, GT) and those whose neonates did not experience intrauterine transmission (control group, GC) analyzed using clone-based sequencing. In total, 206 sequences were successfully amplified, including 98 sequences (from 21 mothers) from GT and 108 sequences (from 20 mothers) from GC of genotype C for mutational analysis. Among the 1203 nucleotides of PreS/S regions, there were 219 (18.20%) base substitutions, of which 103 (47.03%) base mutations caused amino acid changes. F80S, A90V and I68T were mutation hotspots. Mothers in GT had a higher mutation rate of A90V in the PreS1 gene than mothers in GC. The A90V mutation increased the risk of HBV intrauterine transmission after adjusting the maternal age and the mode of delivery (OR = 6.23, 95% CI: 1.18-32.97). Moreover, the area under the ROC curve (AUC) for intrauterine transmission due to A90V and a combination of A90V with the mode of delivery were 0.723 (95% CI: 0.575 to 0.891, P = 0.011) and 0.848 (95% CI: 0.723 to 0.972, P < 0.001), respectively. Mothers with the A90V mutation in the PreS1 gene may be a potential risk factor for HBV intrauterine transmission.

Indexed as

Hepatitis B virusGenotypeHumansInfant, NewbornMutationRisk Factors

Identifiers

PMID37703117
PMCPMC10495115

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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.