Analyses of Sequence Variants in the MYOC Gene and of Single Nucleotide Polymorphisms in the NR3C1 and FKBP5 Genes in Corticosteroid-Induced Ocular Hypertension

Ophthalmic Genet. 2015;36(4):299-302. doi: 10.3109/13816810.2013.879598. Epub 2015 Aug 28.

Abstract

Background: To perform an independent replication study to determine whether genetic variants in MYOC, NR3C1 and FKBP5 are involved in steroid-induced ocular hypertension.

Materials and methods: A retrospective case-control study was peformed on native Dutch patients who were treated with 4.0 mg intravitreal triamcinolone acetonide (IVTA). The patients were divided into an intraocular hypertension group (intraocular pressure >21 mmHg within a year after IVTA) and a non-intraocular hypertension group. The cohort was genotyped for 31 single-nucleotide polymorphisms (SNPs): 21 in NR3C1 and 10 in FKBP5. In addition, the open reading frame of MYOC was sequenced.

Results: A total of 102 patients were included in this study: 58 steroid responders and 44 non-responders. No significant associations were found for the studied SNPs in NR3C1 and FKBP5. Heterozygous amino acid variants were detected in the MYOC gene in two patients of the non-intraocular hypertension group.

Conclusions: This study does not confirm a role for genetic variants in the MYOC, NR3C1 and FKBP5 genes in the pathogenesis of corticosteroid-induced ocular hypertension.

Keywords: FKBP5; MYOC; NR3C1; ocular hypertension/chemically induced; triamcinolone acetonide.

MeSH terms

  • Case-Control Studies
  • Cytoskeletal Proteins / genetics*
  • Eye Proteins / genetics*
  • Gene Frequency
  • Genetic Variation*
  • Genotyping Techniques
  • Glucocorticoids / adverse effects*
  • Glycoproteins / genetics*
  • Humans
  • Intraocular Pressure / drug effects
  • Intravitreal Injections
  • Macular Edema / drug therapy
  • Ocular Hypertension / chemically induced
  • Ocular Hypertension / diagnosis
  • Ocular Hypertension / genetics*
  • Open Reading Frames / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide*
  • Receptors, Glucocorticoid / genetics*
  • Retrospective Studies
  • Tacrolimus Binding Proteins / genetics*
  • Triamcinolone Acetonide / adverse effects

Substances

  • Cytoskeletal Proteins
  • Eye Proteins
  • Glucocorticoids
  • Glycoproteins
  • NR3C1 protein, human
  • Receptors, Glucocorticoid
  • trabecular meshwork-induced glucocorticoid response protein
  • Tacrolimus Binding Proteins
  • tacrolimus binding protein 5
  • Triamcinolone Acetonide