Absence of GSTT1 and polymorphisms in GSTP1 and TP53 are associated with the incidence of acne vulgaris

Skin Res Technol. 2023 Apr;29(4):e13333. doi: 10.1111/srt.13333.

Abstract

Backgrounds: Acne vulgaris is a chronic inflammatory skin disease of the pilosebaceous unit affecting most teenagers and numerous adults throughout the world. The present study was designed to assess the association of the presence or absence of GSTM1, GSTT1, and single nucleotide polymorphisms rs1695 in GSTP1 and rs1042522 in TP53 gene with acne vulgaris.

Methods: The cross-sectional case-control study was conducted at the Institute of Zoology from May 2020 to March 2021 and included acne vulgaris patients (N = 100) and controls (N = 100) enrolled in Dera Ghazi Khan district, Pakistan. Multiplex and tetra-primer amplification refractory mutation system-polymerase chain reactions were applied to investigate the genotype in analyzed genes. The association of rs1695 and rs1042522 with acne vulgaris was studied either individually or in various combinations with GATM1 and T1.

Results: A significant association of absence of GSTT1 and mutant genotype at rs1695 (GG) and at rs1042522 (CC) in GSTP1 and TP53, respectively, was found to be associated with acne vulgaris in enrolled subjects. Subjects aged 10-25 years and smokers were more susceptible to acne vulgaris.

Conclusion: Our results suggest that genotypes of glutathione S-transferases (GSTs) and TP53 are involved in protection against oxidative stress and may influence disease progression in acne vulgaris.

Keywords: GSTM1; GSTT1; acne vulgaris; rs1042522 inTP53; rs1695 in GSTP1.

MeSH terms

  • Acne Vulgaris* / epidemiology
  • Acne Vulgaris* / genetics
  • Adolescent
  • Adult
  • Case-Control Studies
  • Cross-Sectional Studies
  • Genetic Predisposition to Disease* / genetics
  • Glutathione S-Transferase pi / genetics
  • Glutathione Transferase / genetics
  • Glutathione Transferase / metabolism
  • Humans
  • Incidence
  • Risk Factors
  • Tumor Suppressor Protein p53 / genetics

Substances

  • Glutathione Transferase
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • GSTP1 protein, human
  • Glutathione S-Transferase pi