Association of Nucleostemin Polymorphisms with Chronic Hepatitis B Virus Infection in Chinese Han Population

Jixia Li1, Jinya Xu2, Yangui Wang1

  • 1Department of Clinical Laboratory, Yantaishan Hospital, Yantai, China.

Insights

Genetic variants in the nucleostemin (NS) gene are linked to chronic hepatitis B virus infection (CHB) risk in the Chinese Han population. These NS gene variations may serve as potential biomarkers for CHB susceptibility.

Area of Science:

  • Genetics
  • Hepatology
  • Infectious Diseases

Background:

  • Chronic hepatitis B virus infection (CHB) presents a significant global health and economic challenge.
  • Host genetic factors are recognized as crucial determinants of CHB susceptibility and disease progression.
  • The role of specific gene variants in CHB pathogenesis requires further elucidation.

Purpose of the Study:

  • To investigate the association between genetic variations in the nucleostemin (NS) gene and the susceptibility to CHB.
  • To identify potential genetic biomarkers for CHB risk within the Chinese Han population.

Main Methods:

  • Genotyping of four single nucleotide polymorphisms (SNPs) in the NS gene among 446 CHB patients and 399 healthy controls.
  • Utilized polymerase chain reaction-ligation detection reaction (PCR-LDR) for SNP analysis.
  • Performed Bonferroni correction and gender-specific analyses for statistical validation.

Main Results:

  • Three SNPs (rs3733039, rs1866268, rs11177) in the NS gene showed significant association with CHB.
  • The association of rs3733039 with CHB remained significant after Bonferroni correction.
  • Gender-specific analysis revealed associations in both male and female subgroups, with distinct SNP associations observed between genders after multiple comparison corrections.
  • Haplotype analysis identified significant associations for C-C-G and T-T-T haplotypes within the rs3733039-rs1866268-rs11177 block.

Conclusions:

  • This study provides the first evidence of a genetic association between NS gene SNPs and CHB risk in the Chinese Han population.
  • Variations within the NS gene may represent novel genetic biomarkers for predicting CHB susceptibility.
  • Further research is warranted to explore the functional implications of these NS gene variants in CHB pathogenesis.

Related Concept Videos

Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
16.0K
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
11.9K
The Nucleolus02:55

The Nucleolus

The nucleolus is the most prominent substructure of the nucleus. When it was first discovered, it was considered to be an isolated organelle that forms fibrils and granules. In 1931, the relationship between the nucleolus and chromosomes was first described by Heitz. He observed that the appearance and size of nucleolus varies depending on the stage of the cell cycle. He also noticed constricted regions on different chromosomes clustered together at definite cell cycle stages. These regions,...
9.2K
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
14.4K