The relationship between HDAC6, CXCR3, and SIRT1 genes expression levels with progression of primary open-angle glaucoma

Ophthalmic Genet. 2018 Jun;39(3):325-331. doi: 10.1080/13816810.2018.1432061. Epub 2018 Jan 31.

Abstract

Background: Primary open-angle glaucoma (POAG) belongs to neurodegenerative diseases. Its etiology is not fully understood. However, a lot of reports have indicated that many biochemical molecules are involved in the retinal ganglion cell damage. Therefore, the purpose of this study was to evaluate a relationship between HDAC6, CXCR3, and SIRT1 genes expression levels with the occurrence risk of POAG and its progression.

Materials and methods: The study included 34 glaucoma patients and 32 subjects without glaucoma symptoms. RNA was isolated from peripheral blood lymphocytes. Level of mRNA expression was determined by real-time PCR method.

Results: Our results have shown significant association of the HDAC6 and SIRT1 expression levels with progression of POAG according to rim area (RA) value, p = 0.041; p = 0.012. Moreover, the analysis of the CXCR3 expression level showed a correlation with progression of POAG based on RA and cup disc ratio (c/d) value, p = 0.006 and p = 0.012, respectively.

Conclusions: The expression level of HDAC6, CXCR3, and SIRT1 genes may be involved in the progression of POAG.

Keywords: Genes expression; glaucoma; neurodegeneration; progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Biomarkers / analysis*
  • Case-Control Studies
  • Disease Progression
  • Female
  • Gene Expression Regulation
  • Glaucoma, Open-Angle / genetics
  • Glaucoma, Open-Angle / pathology*
  • Histone Deacetylase 6 / genetics*
  • Histone Deacetylase 6 / metabolism
  • Humans
  • Male
  • Receptors, CXCR3 / genetics*
  • Receptors, CXCR3 / metabolism
  • Sirtuin 1 / genetics*
  • Sirtuin 1 / metabolism

Substances

  • Biomarkers
  • CXCR3 protein, human
  • Receptors, CXCR3
  • SIRT1 protein, human
  • Sirtuin 1
  • HDAC6 protein, human
  • Histone Deacetylase 6