Interaction analysis of gene variants related to one-carbon metabolism with chronic hepatitis B infection in Chinese patients

J Gene Med. 2021 Aug;23(8):e3347. doi: 10.1002/jgm.3347. Epub 2021 May 10.

Abstract

Background: The risk of chronic hepatitis B (CHB) infection is influenced by aberrant DNA methylation and altered nucleotide synthesis and repair, possibly caused by polymorphic variants in one-carbon metabolism genes. In the present study, we investigated the relationship between polymorphisms belonging to the one-carbon metabolic pathway and CHB infection.

Methods: A case-control study using 230 CHB patients and 234 unrelated healthy controls was carried out to assess the genetic association of 24 single nucleotide polymorphisins (SNPs) determined by mass spectrometry.

Results: Three SNPs, comprising rs10717122 and rs2229717 in serine hydroxymethyltransferase1/2 (SHMT2) and rs585800 in betaine-homocysteine S-methyltransferase (BHMT), were associated with the risk of CHB. Patients with DEL allele, DEL.DEL and DEL.T genotypes of rs10717122 had a 1.40-, 2.00- and 1.83-fold increased risk for CHB, respectively. Cases inheriting TA genotype of rs585800 had a 2.19-fold risk for CHB infection. The T allele of rs2229717 was less represented in the CHB cases (odds ratio = 0.66, 95% confidence interval = 0.48-0.92). The T allele of rs2229717 was less in patients with a low hepatitis B virus-DNA level compared to the control group (odds ratio = 0.49, 95% confidence interval = 0.25-0.97) and TT genotype of rs2229717 had a significant correlation with hepatitis B surface antigen level (p = 0.0195). Further gene-gene interaction analysis showed that subjects carrying the rs10717122 DEL.DEL/DEL.T and rs585800 TT/TA genotypes had a 2.74-fold increased risk of CHB.

Conclusions: The results of the present study suggest that rs10717122, rs585800 and rs2229717 and gene-gene interactions of rs10717122 and rs585800 affect the outcome of CHB infection, at the same time as indicating their usefulness as a predictive and diagnostic biomarker of CHB infection.

Keywords: SNP; chronic hepatitis B infection; one-carbon metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / genetics
  • Adenosylhomocysteinase / genetics
  • Adult
  • Asian People / genetics
  • Betaine-Homocysteine S-Methyltransferase / genetics*
  • Carbon / metabolism*
  • Case-Control Studies
  • DNA Modification Methylases / genetics
  • DNA Repair Enzymes / genetics
  • Female
  • Genetic Predisposition to Disease
  • Glycine Hydroxymethyltransferase / genetics*
  • Glycine N-Methyltransferase / genetics
  • Hepatitis B, Chronic / genetics*
  • Hepatitis B, Chronic / metabolism
  • Humans
  • Male
  • Methionine Adenosyltransferase / genetics
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Tumor Suppressor Proteins / genetics

Substances

  • Tumor Suppressor Proteins
  • Carbon
  • MTHFR protein, human
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • DNA Modification Methylases
  • 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
  • MTR protein, human
  • GNMT protein, human
  • Glycine N-Methyltransferase
  • BHMT protein, human
  • Betaine-Homocysteine S-Methyltransferase
  • MGMT protein, human
  • Glycine Hydroxymethyltransferase
  • SHMT protein, human
  • MAT2A protein, human
  • Methionine Adenosyltransferase
  • AHCY protein, human
  • Adenosylhomocysteinase
  • DNA Repair Enzymes