Correlation analysis of latent hepatitis B virus infection gene mutation in unpaid blood donors

Abstract

Objective To analyze the HBV S region gene mutation in serum samples of occult hepatitis B virus (HBV) infection (OB1), and to further analyze the mechanism of gene mutation and OBI.

Methods Blood samples from unpaid blood donors from January 2022 to December 2023 were collected and analyzed for serology, liver function indicators, viral load and gene mutation.

Results A total of 90 OBI cases were detected, the detection rate was 0.051%, and the incidence of OBI was correlated with age. The sequence amplification of s region in the blood samples showed the presence of C type and B type genes, both of which occurred in the hydrophilic region.

Conclusion There is no abnormal liver function between OBI and hepatitis B population, and there is no difference in viral load between different serum modes. Mutations in the HBVS region are more likely to cause OBI, which provides a scientific basis for more sensitive HBV detection.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethic Committee of Jiangxi Province Blood Center gave ethical approval of this work

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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