Correlation between CAT polymorphism and susceptibility to DMAc-induced abnormal liver function: a case-control study of Chinese population

Biomarkers. 2018 Mar;23(2):147-153. doi: 10.1080/1354750X.2017.1360942. Epub 2017 Aug 14.

Abstract

Context: Acute or chronic exposure of N,N-dimethylacetamide (DMAc) is responsible for abnormal liver function. It appears that DMAc is mainly metabolized by cytochrome P450 in the liver and thereby produces reactive oxygen species (ROS). The elimination of ROS and the repairing of ROS-induced DNA damage are relevant to the ultimate toxicity of DMAc.

Objective: To investigate whether the polymorphisms in the CAT (rs564250, rs769214 and rs7943316), hOGG1 (rs2072668 and rs159153) and XRCC1 (rs25487 and rs1799782) genes are associated with susceptibility to DMAc-induced abnormal liver function in Chinese population.

Methods: Samples were obtained from 108 workers with DMAc-induced abnormal liver function and 108 workers with normal liver function.

Results: Subjects with the CAT rs769214 GA/GG genotypes had a reducing risk of abnormal liver function, which was more evident in the subgroups exposed to DMAc <10 years, exposed to DMAc <5 mg/m3, never smoked and never drank.

Conclusions: CAT rs769214 (-844 G > A) polymorphism may be associated with DMAc-induced abnormal liver function in Chinese population.

Keywords: CAT; N,N-dimethylacetamide; XRCC1; hOGG1; polymorphism.

MeSH terms

  • Acetamides / poisoning
  • Adult
  • Asian People / genetics
  • Case-Control Studies
  • Catalase / genetics*
  • Chemical and Drug Induced Liver Injury / ethnology
  • Chemical and Drug Induced Liver Injury / etiology
  • Chemical and Drug Induced Liver Injury / genetics*
  • China
  • DNA Glycosylases / genetics
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease / ethnology
  • Genetic Predisposition to Disease / genetics*
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Occupational Exposure / adverse effects
  • Polymorphism, Single Nucleotide*
  • Risk Factors
  • X-ray Repair Cross Complementing Protein 1 / genetics

Substances

  • Acetamides
  • X-ray Repair Cross Complementing Protein 1
  • XRCC1 protein, human
  • Catalase
  • DNA Glycosylases
  • oxoguanine glycosylase 1, human
  • dimethylacetamide